by Madalina Diaconu, Business Development Manager, EW Nutrition GmbH, and Maria Angeles Rodriguez, Gut Health Platform Manager, EW Nutrition GmbHABSTRACT
Avian coccidiosis, caused by intracellular protozoan parasites of the genus Eimeria, remains one of the most economically damaging diseases in commercial poultry production, costing the global industry an estimated USD 10–14 billion annually. For decades, disease management relied on seven recognized Eimeria species infecting chickens. However, the formal characterization in 2021 of three previously cryptic species – Eimeria lata, Eimeria nagambie, and Eimeria zaria – has fundamentally altered this landscape. These newly described parasites are pathogenic, capable of compromising bodyweight gain, and critically, they evade immunity induced by all currently available commercial anticoccidial vaccines. This white paper reviews the biology and epidemiology of these emerging species, examines the limitations of conventional control strategies, and presents the scientific rationale for phytogenic compounds as a complementary, resistance-resilient solution. Specific attention is given to the mechanisms of action of saponins, tannins, thymol, cinnamaldehyde, cumin, licorice, and others against Eimeria infection, intestinal inflammation, and secondary pathogen susceptibility.

1. Introduction: A shifting coccidiosis landscape

Coccidiosis, driven by Eimeria spp. infection of the intestinal epithelium, causes morbidity through hemorrhagic or malabsorptive diarrhea, disrupted gut microbiota, and impaired immune responses. Even subclinical infections exert measurable production costs through reduced bodyweight gain, deteriorated feed conversion ratios (FCR), and heightened susceptibility to secondary pathogens – most notably Clostridium perfringens (necrotic enteritis). The disease is ubiquitous: Eimeria oocysts are environmentally resilient, highly reproductive, and transmitted via fecal-oral routes in all commercial production systems.

For more than seven decades, the field recognized seven Eimeria species as the causative agents of avian coccidiosis in chickens: E. acervulina, E. brunetti, E. maxima, E. mitis, E. necatrix, E. praecox, and E. tenella. Each species infects a distinct region of the intestinal tract and produces characteristic pathological signatures. This taxonomy formed the basis for all commercial coccidiosis vaccines and the design of anticoccidial rotation programs.

In 2021, this foundational assumption was overturned. A landmark study by Blake et al. formally named three cryptic species – previously described only as operational taxonomic units (OTUs) x, y, and z – as Eimeria lata, Eimeria nagambie, and Eimeria zaria. This discovery, enabled by next-generation genomic sequencing, has critical implications for every layer of coccidiosis control: diagnostics, vaccination, and pharmacological management.Economic context
Avian coccidiosis costs the global poultry industry approximately £10.4 billion annually at 2016 prices (Blake et al., 2020). These losses include poor growth performance, treatment costs, increased feed consumption, increased replacement of chicks, and enhanced susceptibility to concurrent infections such as necrotic enteritis.

2. The three new Eimeria species: Biology, pathogenicity, and global spread

2.1 Discovery and formal classification

The three cryptic Eimeria OTUs were first identified through molecular epidemiological surveys in Australia in 2007–2008 (Cantacessi et al., 2008). Initially named OTU-X, OTU-Y, and OTU-Z, these genotypes showed consistent genetic divergence from the seven recognized species but lacked formal biological characterization. Blake et al. (2021), working at the Royal Veterinary College (UK), conducted an exhaustive characterization combining oocyst morphology, pre-patent periods, pathology, and draft genome sequence assemblies. The conclusion was unambiguous: all three OTUs possess sufficient genetic and biological diversity to constitute new species.

The three new species were named:

Eimeria lata n. sp. (formerly OTU-X): Named for its unusually wide oocyst morphology – the broadest average oocyst width of any Eimeria species infecting chickens.

Eimeria nagambie n. sp. (formerly OTU-Y): Named after Nagambie, Victoria, Australia, the location of the first isolate.

Eimeria zaria n. sp. (formerly OTU-Z): Named after Zaria, Nigeria, reflecting the geographic origin of its initial isolation.

Figure 1. Sporulated oocysts of the Eimeria Operational Taxonomic Unit (OTU) genotypes x, y, and z collected from domestic chickens (Gallus gallus domesticus). Photomicrographs of sporulated oocysts are shown for (A) OTUx, (B) OTUy and (C) OTUz. Composite line drawings are shown for (D) OTUx, (E) OTUy and (F) OTUz. RB, residual body; SB, stieda body; PG, polar granule. Scale bars = 10 µm. © 2021 Blake et al., Int J Parasitol. 2021 Jul;51(8):621–634. doi: 10.1016/j.ijpara.2020.12.004

2.2 Pathogenicity and production impact

Experimental infection trials demonstrated that all three new species are capable of compromising broiler bodyweight gain, a direct measure of economic impact. Unlike historically recognized species such as E. acervulina and E. tenella, whose pathological signatures are well-characterized, the intestinal tropism and precise pathological mechanisms of E. lata, E. nagambie, and E. zaria remain under active investigation. Their clinical presentation may overlap with existing species, complicating field diagnosis through standard lesion scoring alone.
The Eimeria-gut microbiota interaction is particularly relevant here. Research has demonstrated that Eimeria infection disrupts intestinal bacterial communities, reducing beneficial taxa and creating dysbiosis conditions that facilitate opportunistic bacterial overgrowth – most critically by C. perfringens. The bidirectional interaction between coccidiosis and necrotic enteritis leads to cumulative economic burdens. However, it remains to be determined whether the newly identified species possess distinct microbiota-modulating profiles.

2.3 Geographic distribution and diagnostic blind spots

Initially considered geographically restricted to the Southern Hemisphere, detection has since expanded significantly. One or more of the three new species have now been confirmed in Australia, multiple sub-Saharan African countries, India, Venezuela, the United States, and – as of 2023 – Europe, with the first reported detection of E. zaria in European broiler flocks (Jaramillo-Ortiz et al., 2023). The heavy reliance of existing diagnostic protocols on oocyst morphology and PCR panels developed for the original seven Eimeria species raises concerns that newly identified species are routinely underdetected in field surveillance.Critical diagnostic gap
Standard coccidiosis diagnostics – including lesion scoring, oocyst morphology, and many commercial PCR kits – were designed around the seven classical Eimeria species. E. lata, E. nagambie, and E. zaria may circulate undetected in flocks, contributing to unexplained performance losses and vaccine failures. Next-generation sequencing (NGS) targeting 18S rRNA is currently the most reliable identification tool (Blake et al., 2021).

2.4 Vaccine evasion: The central challenge

The most commercially disruptive characteristic of the three new species is their demonstrated ability to evade immunity induced by all currently available commercial anticoccidial vaccines. Live attenuated coccidiosis vaccines, the cornerstone of antibiotic-free coccidiosis control programs, are designed against the original seven species. Experimental challenge studies confirmed that prior vaccination provides no protective immunity against E. lata, E. nagambie, or E. zaria (Blake et al., 2021). This creates a significant vulnerability in integrated coccidiosis control programs, particularly in broiler production systems where vaccination programs are used as the primary long-term resistance management strategy.

The inability of current vaccines to address these new species underscores a critical need for broad-spectrum, mechanism-resilient complementary tools. Phytogenic compounds, acting through multiple simultaneous mechanisms, represent an ideal candidate for this role.

3. Current control strategies and their limitations

3.1 Chemical anticoccidials and ionophores

Chemical anticoccidials (e.g., diclazuril, toltrazuril, amprolium) and ionophore antibiotics (e.g., monensin, salinomycin) remain the primary pharmaceutical tools for coccidiosis control globally. These compounds target specific metabolic or ion transport mechanisms in Eimeria and have historically been highly effective when deployed in rotational shuttle programs. However, decades of continuous use have driven the emergence of resistance across multiple drug classes. Field resistance to monensin, robenidine, salinomycin, maduramicin, and diclazuril has been extensively documented across multiple geographic regions (Ferdji et al., 2022; Flores et al., 2022).

Resistance development occurs through multiple mechanisms: altered cell membrane permeability reducing drug uptake, use of alternative biochemical pathways, mutations at drug target sites, and genetic recombination within Eimeria populations. Crucially, resistance to one drug class does not necessarily confer resistance to compounds with different mechanisms – providing the theoretical basis for rotation programs. However, field conditions, partial compliance, and concurrent use often undermine the protective effects of rotation strategies.

3.2 Vaccines: Effective but incomplete

Live attenuated and live non-attenuated coccidiosis vaccines have represented a major advance in resistance management, offering cycle-by-cycle immunity development without driving pharmacological resistance. In broiler production, their use has grown significantly in recent years, particularly in no-anticoccidial or antibiotic-free production systems. However, as established in Section 2.4, no current commercial vaccine confers immunity against E. lata, E. nagambie, or E. zaria. This gap is not a minor caveat – it means that a vaccinated flock may be fully protected against classical species while remaining completely susceptible to the three newly described ones.

3.3 The regulatory and consumer pressure context

Across the European Union and in growing markets globally, regulatory restrictions on preventive antibiotic use, ionophore limitations in organic systems, and consumer demand for residue-free products have created strong incentives to explore alternatives. The combination of resistance pressure, vaccine limitations against new species, and regulatory trends makes the case for phytogenic integration both scientifically and commercially compelling.

4. Phytogenics as a multi-mechanism solution

4.1 Why phytogenics are relevant for coccidiosis control

Phytogenic compounds – plant-derived bioactive molecules including essential oil components, polyphenols, saponins, tannins, alkaloids, and bitter glycosides – have gained substantial scientific attention as a class of natural feed additives with demonstrated antimicrobial, antiparasitic, antioxidant, and immunomodulatory properties. Their relevance to coccidiosis management is grounded in three complementary properties: (1) direct antiparasitic action against Eimeria oocysts, sporozoites, and intracellular stages; (2) protection and restoration of intestinal mucosal integrity following Eimeria-induced damage; and (3) modulation of host immune responses to improve resilience against both Eimeria and secondary pathogens.

A key advantage of phytogenic compounds over conventional anticoccidials is their multi-target mode of action. Because each active molecule typically acts on multiple biological pathways simultaneously, the probability of resistance development through a single mutation is substantially lower than for single-target drugs. Furthermore, the inclusion of phytogenic blends in programs alongside vaccines or anticoccidials can provide synergistic or additive coverage – particularly relevant now that three new Eimeria species fall outside the protective scope of all available vaccines.

4.2 Compound-specific mechanisms of action

The following section reviews the scientific evidence for eight key phytogenic compounds relevant to coccidiosis control. A summary table is presented at the end of this section.

Saponins

Saponins are amphiphilic glycosides found in diverse plant species including Quillaja saponaria and Yucca schidigera. Their anticoccidial activity is primarily attributable to their capacity to interact with and disrupt lipid bilayer membranes. In the context of Eimeria, this membrane-disrupting action weakens the structural integrity of the parasite’s outer protective layers, rendering it more vulnerable to host immune effectors. Importantly, saponins also impair Eimeria attachment to intestinal epithelial cells, interrupting the invasion cascade. Bafundo et al. (2020) demonstrated that broilers receiving Quillaja/Yucca-derived saponin diets showed significantly reduced oocyst counts and improved weight gain compared to untreated controls challenged with Eimeria spp. Abbas et al. (2012), in a comprehensive botanical review, concluded that saponins significantly reduce both oocyst shedding and intestinal lesion scores, with efficacy approaching that of conventional anticoccidials.

Tannins

Tannins are polyphenolic compounds classified as condensed (proanthocyanidins) or hydrolysable (ellagitannins, gallotannins), found in chestnut, quebracho, and oak, among others. Their antiparasitic action against Eimeria involves protein precipitation at the parasite cell membrane – a non-specific mechanism that does not readily lend itself to resistance development. Tannins also exert strong antioxidant activity, directly reducing oxidative stress in intestinal tissue damaged by Eimeria – a crucial function given that lipid peroxidation is a primary driver of mucosal injury in coccidiosis. Masood et al. (2013) confirmed that tannin supplementation reduced intestinal oxidative stress and improved performance in broilers challenged with Eimeria. Abbas et al. (2012) further established their equivalence to chemical anticoccidials in reducing lesion severity and oocyst output.

Thymol (Thyme, Thymus vulgaris)

Thymol, the principal bioactive phenol of Thymus vulgaris essential oil, has been extensively studied for its anticoccidial properties. In vitro work by Remmal et al. (2013) demonstrated that thymol disrupts oocyst structural integrity and inhibits sporulation at concentrations of ≥2%, with maximal oocyst degeneration rates reaching 96% at 10%. At the level of intracellular parasite development, thyme essential oil was shown to inhibit the first round of schizogony in E. tenella with efficacy comparable to commercial anticoccidial drugs. Beyond direct antiparasitic action, thyme essential oil significantly downregulates pro-inflammatory mediators in Eimeria-challenged systems, reducing immune-mediated intestinal damage without suppressing protective immunity (Felici et al., 2024).

Cinnamaldehyde (Cinnamon, Cinnamomum verum)

Cinnamaldehyde, the principal aldehyde constituent of cinnamon bark, inhibits E. tenella sporozoite invasion of Madin-Darby bovine kidney (MDBK) epithelial cells in vitro, as part of a broader phenolic compound class with documented anti-invasion activity against Eimeria (Sidiropoulou et al., 2020). It reduces oocyst sporulation by approximately 79% in vitro (Remmal et al., 2013). Particularly notable is the synergistic effect between cinnamaldehyde and carvacrol (the active component of oregano oil): when used in combination, they achieve approximately 90% reduction in oocyst viability – substantially superior to either compound alone. This synergism supports the formulation of multi-compound blends. Cinnamaldehyde also demonstrates significant antimicrobial activity against Clostridium perfringens, providing simultaneous protection against the primary secondary pathogen associated with coccidiosis-driven necrotic enteritis.

Cumin (Cuminaldehyde, Cuminum cyminum)

Cumin seed contains cuminaldehyde as its primary bioactive compound, alongside cymene and other phenolic constituents. The anticoccidial relevance of cumin derives from multiple overlapping mechanisms: phenolic compounds interact with Eimeria oocyst membranes in a manner analogous to tannins, disrupting cytoplasmic membrane integrity and causing parasite cell death. Antioxidant properties protect intestinal epithelial cells from oxidative damage following Eimeria invasion. Broad-spectrum antimicrobial activity against common poultry pathogens, including C. perfringens, Salmonella spp., and E. coli, addresses the bacterial gateway mechanisms that amplify Eimeria-associated pathology. El-Shall et al. (2022) and the phytochemical coccidiosis control review (El-Shall et al., 2022) confirm cumin among the botanicals with documented anticoccidial and mucoprotective activity.

Licorice (Glycyrrhizin, Glycyrrhiza glabra)

Licorice root, through its primary bioactive compound glycyrrhizin and associated flavonoids (liquiritin, isoliquiritigenin), exerts potent immunomodulatory and anti-inflammatory effects particularly relevant to Eimeria-associated pathology. Glycyrrhizin stimulates T-cell mediated immune responses – the primary adaptive immune mechanism governing protective immunity against Eimeria – while modulating excessive inflammatory cascades that cause collateral intestinal damage. This dual action (immune stimulation + anti-inflammatory) is uniquely valuable in coccidiosis: it supports the development of parasite-specific immunity while limiting tissue destruction. Licorice compounds also support intestinal epithelium repair following Eimeria-induced villous atrophy, contributing to faster restoration of absorptive surface and productive performance. The immunomodulatory profile of licorice makes it particularly relevant as a complement to anticoccidial vaccination programs – supporting the immune priming process against classical species while potentially reinforcing innate defenses against the new, vaccine-evading species.

The right phytogenics can support coccidiosis control

Fig. 1 Lesion scores by intestinal segment. All treatments reduced lesion scores significantly compared to the positive control, but the Phytogenic was the clear winner overall, especially dominant in the caeca (E. tenella). Notably, the phytogenic products outperformed the coccidiostat on total lesion score, which is a strong result, particularly because the coccidiostat struggled against E. tenella in the caeca, where Phytogenic excelled.

Fig. 2 Microbiota recovery by day 18 pi. All four treatment groups performed similarly and dramatically better than the untreated positive control, reducing the dysbacteriosis score by roughly 45–49% compared to the positive control. The differences between the treated groups are minor and likely not statistically significant, meaning the phytogenic products performed on par with the coccidiostat in protecting gut health after Eimeria infection.

4.3 Summary: Phytogenic compound mechanisms at a glance

5. Integration into coccidiosis control programs

5.1 Phytogenics in combination with vaccines

The ideal integration model for phytogenics in the context of the new Eimeria species is as a permanent background layer within any coccidiosis control program – regardless of whether that program is vaccine-based, chemical-based, or a shuttle combination. For vaccinated flocks, phytogenics provide complementary activity against E. lata, E. nagambie, and E. zaria – species against which vaccines offer no protection – while supporting the immune priming process for species covered by the vaccine. Their immunomodulatory effects (particularly licorice and thyme) optimize T-cell responses during the vaccination window.

5.2 Phytogenics in chemical anticoccidial programs

In flocks managed with chemical anticoccidials, phytogenics serve a dual function: reducing the parasite load and oocyst environmental contamination (through saponins, tannins, cinnamaldehyde, and anise), and protecting intestinal integrity during chemotherapy-related periods when mucosal recovery is needed. Given the documented resistance issues with current chemical classes, the multi-mechanism action of phytogenic blends provides coverage that complements rather than competes with pharmacological programs.

5.3 Resistance management and sustainability

A defining advantage of multi-component phytogenic blends is their resistance resilience. Because compounds such as saponins, tannins, essential oil phenols, and bitter glycosides act on multiple biological targets simultaneously – membrane integrity, cell adhesion, sporulation, immune activation, oxidative balance – the probability of Eimeria developing resistance to a well-formulated phytogenic blend is fundamentally lower than for single-target anticoccidials. As regulatory pressure on chemical anticoccidials increases globally, particularly in the EU, phytogenic integration offers a scientifically grounded pathway to sustainable, long-term coccidiosis management.Key message for integrators and veterinarians
The characterization of E. lata, E. nagambie, and E. zaria creates a non-negotiable gap in current vaccine-based control programs. No available commercial vaccine provides protection against these three new species. Phytogenic blends – specifically those combining saponins, tannins, thymol, cinnamaldehyde, and supporting compounds (cumin, licorice, etc.) – offer the only currently available broad-spectrum complementary tool capable of addressing this gap while simultaneously managing drug-resistant classical species.

6. Conclusions

The formal naming of Eimeria lata, Eimeria nagambie, and Eimeria zaria in 2021 represents the most significant taxonomic development in avian coccidiosis in decades. Beyond nomenclature, these new species present concrete operational challenges: they are pathogenic, performance-impairing, capable of global spread, and invisible to all currently available commercial vaccines and most routine diagnostic protocols.

This discovery reinforces the case for moving beyond single-mechanism control strategies. Phytogenic compounds, through their complementary and multi-target mechanisms of action, provide a scientifically validated layer of broad-spectrum coccidiosis management. The compound portfolio reviewed in this paper – saponins, tannins, thymol, cinnamaldehyde, cumin, licorice, etc. – collectively addresses direct parasite suppression, intestinal barrier protection, immune modulation, oxidative stress reduction, and secondary pathogen control. These mechanisms operate independently of vaccine-induced immunity and without the resistance trajectories associated with conventional anticoccidials.

As the global poultry industry adapts to a coccidiosis landscape that now includes ten recognized Eimeria species infecting chickens, phytogenic integration is no longer an optional enhancement – it is a fundamental component of resilient, future-proof flock health management.

For more information on EW Nutrition’s phytogenic solutions supporting coccidiosis control,
contact your EW Nutrition regional representative or visit ew-nutrition.com

References

Abbas, R.Z., Colwell, D.D., Gilleard, J. (2012). Botanicals: an alternative approach for the control of avian coccidiosis. World’s Poultry Science Journal, 68(2), 203–215.

Abbas, R.Z., Iqbal, Z., Blake, D., Khan, M.N., Saleemi, M.K. (2011). Anticoccidial drug resistance in fowl coccidia: the state of play revisited. World’s Poultry Science Journal, 67(2), 337–350.

Bafundo, K.W., Johnson, A.B., Mathis, G.F. (2020). The effects of a combination of Quillaja saponaria and Yucca schidigera on Eimeria spp. in broiler chickens. Avian Diseases, 64(3), 300–304.

Blake, D.P., Knox, J., Dehaeck, B., Huntington, B., Rathinam, T., Ravipati, V., Ayoade, S., Gilbert, W., Adebambo, A.O., Tiambo, C.K., Tomley, F.M. (2020). Re-calculating the cost of coccidiosis in chickens. Veterinary Research, 51, 115.

Blake, D.P., Marugan-Hernandez, V., Tomley, F.M. (2021). Spotlight on avian pathology: Eimeria and the disease coccidiosis. Avian Pathology, 50(3), 209–213.

Blake, D.P., Vrba, V., Xia, D., Jatau, I.D., Spiro, S., Nolan, M.J., Underwood, G., Tomley, F.M. (2021). Genetic and biological characterisation of three cryptic Eimeria operational taxonomic units that infect chickens (Gallus gallus domesticus). International Journal for Parasitology, 51(8), 621–634.

Cantacessi, C., Riddell, S., Morris, G.M., Doran, T., Woods, W.G., Otranto, D., Gasser, R.B. (2008). Genetic characterization of three unique operational taxonomic units of Eimeria from chickens in Australia based on nuclear spacer ribosomal DNA. Veterinary Parasitology, 152(3–4), 226–234.

El-Shall, N.A., Abd El-Hack, M.E., Albaqami, N.M., Khafaga, A.F., Taha, A.E., Swelum, A.A., El-Saadony, M.T., Salem, H.M., El-Tahan, A.M., AbuQamar, S.F., El-Tarabily, K.A., Elbestawy, A.R. (2022). Phytochemical control of poultry coccidiosis: a review. Poultry Science, 101(1), 101542.

Felici, M., Tugnoli, B., De Hoest-Thompson, C., Piva, A., Grilli, E., Marugan-Hernandez, V. (2024). Thyme, oregano, and garlic essential oils and their main active compounds influence Eimeria tenella intracellular development. Animals, 14(1), 77.

Ferdji, F., Zahraoui-Mehadji, M., Baazizi, R., Meghit-Boumediene, K. (2022). Anticoccidial drug resistance in Eimeria field isolates from broiler farms in western Algeria. Veterinary Parasitology: Regional Studies and Reports, 32, 100733.

Flores, M.I., Saldana, B., Orozco, M.M., Quijada, N.M., Bersosa, F., Mateo, E. (2022). Anticoccidial resistance to chemical compounds and ionophores in Eimeria field isolates from commercial broiler farms. Poultry Science, 101(11), 102180.

Hailat, A.M., Abdelqader, A.M., Gharaibeh, M.H. (2024). Efficacy of phyto-genic products to control field coccidiosis in broiler chickens. International Journal of Veterinary Science, 13(3), 266–272.

Jaramillo-Ortiz, J.M., Burrell, C., Adeyemi, O., Werling, D., Blake, D.P. (2023). First detection and characterisation of Eimeria zaria in European chickens. Veterinary Parasitology, 323, 109857.

Masood, S., Abbas, R.Z., Iqbal, Z., Mansoor, M.K., Sindhu, Z.U.D., Zia, M.A., Khan, J.A. (2013). Role of natural antioxidants for the control of coccidiosis in poultry. Pakistan Veterinary Journal, 33(4), 401–407.

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Remmal, A., Achahbar, S., Bouddine, L., Chami, F., & Chami, N. (2013). Oocysticidal effect of essential oil components against chicken Eimeria oocysts. International Journal of Veterinary Medicine: Research & Reports, 2013, 599816.

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Sidiropoulou, E., Skoufos, I., Marugan-Hernandez, V., Giannenas, I., Bonos, E., Aguiar-Martins, K., Lazari, D., Blake, D.P., Tzora, A. (2020). In vitro anticoccidial study of oregano and garlic essential oils and effects on growth performance, fecal oocyst output, and intestinal microbiota in vivo. Frontiers in Veterinary Science, 7, 420.

by Ivan Ilić, Application Manager EW Nutrition GmbH

Choosing the right strategy

During global client visits, I frequently observe that the primary objective of a process is disconnected from the subsequent steps and final actions. Choosing a strategy is sometimes done paradoxically – like putting worn-out winter tires on a vehicle just because they are cheap and available in your garage, and then attempting to race in the Paris-Dakar rally. To succeed, you must choose the right race or use the proper equipment; anything else is a waste of time and energy without meaningful results. Let’s examine heat treatment and Salmonella control in feed processing as a prime example.

Moisture is not merely a percentage point in the final product; it is a fundamental component of high-quality feed. While much has been written about its influence on pellet quality, energy efficiency, and starch gelatinization, its role extends much further. Moisture is one of the most critical parameters influencing the effectiveness of Salmonella control in feed manufacturing. Its impact is observed across multiple stages, including thermal treatment, chemical control using organic acids, and post-processing stability during storage and handling.

Thermal processing and microbial resistance

From a thermal processing perspective, moisture directly affects the heat resistance of Salmonella. In low-moisture environments, such as dry feed (10–11% moisture), Salmonella cells exhibit significantly increased thermal resistance. This is primarily because reduced moisture stabilizes cellular structures and limits heat-induced damage. As demonstrated by Gautam et al. (2020), decreasing moisture leads to increased survival of Salmonella during heat exposure. Consequently, higher temperatures or longer retention times are required to achieve equivalent microbial reduction in dry feed.

In contrast, the presence of moisture – especially in the form of steam during conditioning – enhances heat transfer and increases microbial susceptibility. Coe et al. (2022) showed that effective reductions (>6 log₁₀) of Salmonella in feed could be achieved under hydrothermal conditions, confirming that temperature, moisture, and time must be considered together. Moisture facilitates protein denaturation within bacterial cells and disrupts membrane integrity, significantly improving the lethality of heat treatment.

The role of organic acids

Moisture also plays a key role in the efficacy of organic acids used for Salmonella control. Organic acids act primarily through their undissociated form, which penetrates bacterial cell membranes. This mechanism is highly dependent on the presence of water. Liquid acids, already in an aqueous phase, are immediately active and capable of rapid antimicrobial action. Powder acids, on the other hand, require moisture for dissolution, diffusion, and activation. Under dry conditions, their antimicrobial effect is delayed or reduced; however, in conditioned feed, they can approach the efficacy of liquid acids.

When comparing powder versus liquid acids, it is important to distinguish between immediate efficacy in feed hygiene and biological efficacy in the bird. Liquid acids are typically more effective for rapid feed decontamination because they distribute more readily and do not require the same degree of moisture activation. Powder acids and salts may be less aggressive, easier to handle, and more stable during storage, providing a longer-lasting effect against recontamination. However, their performance depends heavily on feed moisture, conditioning, and release characteristics.

In the bird, protected or coated acids may outperform free liquid acids in later gut segments because they are designed to survive the upper digestive tract. Therefore, the definition of ‘better’ depends on the target: surface/feed kill, residual feed hygiene, or gut modulation. Direct comparative evidence remains limited, so this distinction should be viewed as a mechanistic interpretation rather than a universal ranking.

Balancing hygiene and nutritional quality

The interaction between heat treatment and organic acids also affects broiler performance. Research by Goodarzi Boroojeni et al. indicates that thermal processing severity changes nutrient digestibility. Their work shows that harsh conditioning can reduce ileal nutrient digestibility, while organic acid inclusion can improve early feed efficiency and help maintain performance. This is a vital practical point: the most aggressive hygienization strategy is not necessarily the best biological strategy. A feed mill can reduce microbial risk but may lose nutritional value if the thermal load is excessive.

Additionally, moisture improves the distribution and penetration of acids into microenvironments where bacteria may be protected, such as within dust particles or organic matrices. However, excessive moisture can dilute acids and reduce their local concentration. As in many aspects of processing, balance is the key.

Post-process hygiene and recontamination

Reviews of Salmonella in feed manufacturing emphasize that even heat-treated feed may become contaminated again via dust, coolers, conveyors, or storage. While moisture and heat determine the success of the initial ‘kill step,’ post-process hygiene determines whether those gains are maintained. This is why chemical control measures are usually discussed as complements to – not replacements for – hydrothermal processing and mill hygiene.

Practical conclusions

Moisture acts as both an enabler and a risk factor. It enhances heat and acid efficacy during processing but can increase microbial risk if not properly managed after production. Effective Salmonella control requires an integrated approach. The research supports three practical conclusions:

• Moisture significantly enhances the effectiveness of heat treatment; dry feed protects Salmonella and increases its thermal resistance.
• Moisture influences acid efficacy, with powder forms being more moisture-dependent than liquid forms for rapid action.
• Organic acids can support animal performance, particularly body weight gain and feed efficiency.

With products like Surf-Ace, we can achieve increased pellet output, improved conditioning, enhanced durability of the pelleted feed, reduced fines formation, and improved overall quality of the final feed product. However, the best feed hygiene strategy is not to rely on one tool alone, but to also integrate controlled moisture, appropriate thermal treatment, organic acid application (such as Acidomix, whose strong antimicrobial effects help improve feed hygiene and help prevent / control salmonella), and strict post-pellet hygiene into a single cohesive system. We just need to select the right tools to achieve the results we want.

References

Abd El-Ghany, W. A. (2024). Applications of organic acids in poultry production: An updated and comprehensive review. Agriculture, 14(10), 1756. https://doi.org/10.3390/agriculture14101756

Coe, N., Wei, S., Little, C., & Shen, C. (2022). Thermal inactivation of Salmonella surrogate, Enterococcus faecium, in mash broiler feed pelleted in a university pilot feed mill. Poultry Science, 104(5), 104998. https://doi.org/10.1016/j.psj.2025.104998

Gautam, M., Lian, K., Jin, Y., Steinbrunner, P., & Tang, J. (2020). Water activity influence on the thermal resistance of Salmonella in soy protein powder at elevated temperatures. Food Control, 113, 107160. https://doi.org/10.1016/j.foodcont.2020.107160

Goodarzi Boroojeni, F., Mader, A., Knorr, F., Vahjen, W., & Zentek, J. (2014). The effect of different thermal processing methods and carbohydrate sources on performance, nutrient digestibility and the intestinal microbiota of broiler chickens. Poultry Science, 93(5), 1152–1162. https://doi.org/10.3382/ps.2013-03632

Polycarpo, G. V., Burbarelli, M. F., Carão, A. C., Merseguel, C. E., Dadalt, J. C., Magalhães, R., … & Albuquerque, R. (2017). Effects of organic acids, probiotics and antibiotics on performance, gastrointestinal pH, and intestinal morphology of broiler chickens. Poultry Science, 96(1), 127–134. https://doi.org/10.3382/ps/pew270

Tomičić, Z., Čabarkapa, I., Čolović, R., Đuragić, O., & Tomičić, R. (2019). Salmonella in the feed industry: Problems and potential solutions. Journal of Agronomy, Technology and Engineering Management, 2(1), 130–139.

Van Immerseel, F., Russell, J. B., Flythe, M. D., Gantois, I., Timbermont, L., Pasmans, F., … & Ducatelle, R. (2006). The use of organic acids to combat Salmonella in poultry: A mechanistic explanation of the efficacy. Avian Pathology, 35(3), 182–188. https://doi.org/10.1080/03079450600711045

by Ilinca Anghelescu, Global Director Marketing & Communications, EW Nutrition

Every week, a new story promises to change how we eat. Lab-grown steaks. Vertical farms fed by LED lights. Cricket flour. The algae revolution. Regenerative everything.

Meanwhile, somewhere in Iowa, a farmer is managing soil drainage at 4 a.m. In the Yangtze River Delta, flooded paddy fields are being leveled by laser-guided equipment. In the Sahel, sorghum is being harvested by hand under brutal heat. In the Netherlands, greenhouse engineers are coaxing eight tomato harvests a year from hydroponic systems. Such professionals, such practices are, collectively, the reason 8 billion people ate today.

How we got here, and why we cannot go back

The density problem nobody talks about

In his 2024 book How to Feed the World, Czech-Canadian professor and researcher Vaclav Smil notes that, across 300 forager societies that persisted into the 19th and 20th centuries, the mean population density was 0.25 persons per square kilometer.¹ The most productive forager groups, those with access to salmon runs or seal hunting on Pacific coastlines, could reach just above one person per square kilometer. By contrast, intensive agricultural systems in southern China during the Qing dynasty supported more than 500 people per square kilometer of farmland.¹ Contemporary industrial agriculture can support between 500-900.

In Smil’s analysis, agriculture is not slightly more efficient at feeding people than foraging. Agriculture is between 500 and 2,000 times more efficient than foraging.

The thought experiment Smil runs through disposes of several popular fantasies at once, including those in which humans go back to a primitive way of eating. For instance, an adult human eating like a chimpanzee (roughly 80 percent fruit by mass) would need four to five kilograms of ripe fruit daily, requiring hours of foraging and providing almost no fat or protein.¹ To supply just the European Union’s 450 million people with adequate protein via this dietary route would require more than half a billion tons of figs per year, roughly 400 times the entire 2020 global fig harvest.¹ The chimp model, like other primitive models (whether purely foraging or hunting or a mixed model), cannot scale.

In other words, in a world currently trying to feed 8.3 billion people, the transition to agriculture cannot be undone.

The rule of 20: Why we eat so few plants

One of the more counterintuitive facts in food systems science is how narrow our dietary base actually is. Botanists have classified nearly 400,000 species of vascular plants. Roughly 12,000 of those are grasses capable of producing nutritious seeds. Of these, humanity has domesticated a tiny fraction. Just 20 plant species account for 75 percent of all annually harvested crops by weight. Two of those species, rice and wheat, alone supply 35 percent of global food energy.¹

This is not a failure of agricultural imagination but the result of stringent selection criteria that operated over thousands of years. Smil calls these criteria the “entry requirements” for staple crops: fast maturation, high yield, long shelf life, resistance to pests, and high energy density. Wheat, for example, contains roughly 350 kilocalories per 100 grams. Tomatoes contain fewer than 20 kcal/100g. Wheat is 18 times more energy-dense per unit weight.¹

The early civilizations that independently discovered the cereal-legume combination (corn and beans in the Americas, rice and soybeans in Asia, wheat and lentils in the Middle East) were solving an amino acid optimization problem without knowing it. Cereals are low in the essential amino acid lysine. Legumes are high in it. Together, they provide a complete protein profile. The world’s great cuisines, from Mexican rice and beans to Japanese miso soup over rice, are not accidents. They are dietary solutions that natural selection, mediated through human survival and culture, arrived at over millennia.¹

What the economy doesn’t count

The GDP illusion

In standard economic accounting, agriculture contributes roughly 1 to 4 percent of GDP in developed countries and somewhat more in developing ones. This number is cited constantly as evidence that farming is a residual sector, economically marginal, safely neglected in favor of “shinier” industries.

Smil dismantles this framing methodically. When you add food processing, food manufacturing, beverages, food retail, and food service, the food system in the United States accounts for approximately 5 percent of GDP and more than 10 percent of total employment.¹ But even this number, broad as it is, underestimates the true scale, because it fails to capture the full infrastructure dependency: the fuel and energy consumed by agricultural machinery, the chemical industry built to supply fertilizer, the logistics networks dedicated to food transport and cold chain management, and the healthcare costs tied to diet-related disease.

When Smil attempts a full-system accounting of global food, including production, processing, transportation, wholesale, retail, storage, and consumption, he concludes that the food system’s true share of global economic activity is on the order of 25 to 30 percent of respective totals, with standard economic accounts attributing less than 5 percent representing “grossly inaccurate and highly misleading quantifications.”¹

The energy picture is similarly startling. Smil calculates that the global food system consumes between 20 and 25 percent of the world’s annual primary energy supply.¹ This includes the energy to grow, harvest, process, refrigerate, transport, package, cook, and dispose of food. It is the single largest category of energy use in human civilization, larger than personal transportation, larger than industrial manufacturing of most goods, and yet it rarely appears in climate policy discussions with the prominence its scale demands.

Smil offers one striking comparison that has only sharpened since his original analysis. The global smartphone market in 2024 generated approximately $441 billion in wholesale revenue, calculated from approximately 1.24 billion units shipped at a record average selling price of $356.³⁴ In that same year, the global wheat harvest, some 799 million tons, was worth approximately $215 billion at reference export prices, and the global rice harvest of roughly 541 million tons was worth approximately $318 billion.^{32 33} Combined, just these two crops generated an estimated $533 billion, roughly 20 percent more than the entire global smartphone market. Two crops, grown on a fraction of Earth’s farmland, produced economic value that exceeds the most ubiquitous consumer technology device in human history.

Revolutions usually come from empty stomachs

A history lesson worth remembering

The historical relationship between food insecurity and political instability is one of the most robustly documented relationships in social science. The French Revolution of 1789 was preceded by catastrophic grain harvests in 1788. Bread prices in Paris in early 1789 consumed up to 88 percent of a worker’s daily wage.² The Arab Spring of 2010-2011 was triggered, at least in part, by a spike in global food commodity prices. Mohamed Bouazizi, the Tunisian street vendor whose self-immolation catalyzed a regional uprising, was a food vendor who had his produce confiscated.³

The research is consistent. A 2011 preprint study published by Marco Lagi and colleagues at the New England Complex Systems Institute found that global food price spikes, as measured by the FAO Food Price Index, were a consistent precursor to social unrest and political instability events across multiple continents.³ A 2015 paper in the American Journal of Agricultural Economics extended this analysis, finding statistically significant relationships between cereal price levels and social unrest.⁴

The baseline condition for social order is that people have access to food. Everything else, including the liberal democratic institutions, the tech economies, and the climate negotiations that dominate contemporary policy attention, depends on that foundation being intact. Smil makes this point in structural rather than historical terms. When he asks whether smartphones or food matter more, the answer is obvious to him: “A world without smartphones would be poorer and less convenient. A world without food would not exist.”¹

The 9%

According to the UN Food and Agriculture Organization, approximately 733 million people, roughly 9 percent of the global population, were undernourished in 2023.⁵ This is not primarily a production problem. As Smil notes and the FAO confirms, global food production averages around 3,000 kilocalories per person per day, which is substantially above the roughly 2,500 kilocalories required by an average active adult.¹⁵ The world produces enough calories to feed everyone.

The problem is access, poverty, and distribution. Hunger is a political economy failure, as price spikes hit the poor first and hardest. But if global food production fell by 10 percent, the 9 percent who are currently undernourished would not be the only ones suffering. Supply shocks ripple through markets and a globalized world does not allow for compartmentalized impact as much as it used to.

The real environmental cost: Agriculture and alternatives

Some immediate problems have immediate solutions

Agriculture accounts for approximately 72 percent of global freshwater withdrawals.¹ Cropland and permanent pastures together cover about 36 percent of non-glaciated land.¹ The food system is responsible for approximately 34 percent of global greenhouse gas emissions, based on the most comprehensive analysis available.⁶ These figures are often presented as indictments. They should instead be understood as measures of necessity. The question is not “why does food production use so much?” but “what would we use it on instead, and would that work?”

The FAO’s global assessment of livestock’s climate impact, the famous 2006 report Livestock’s Long Shadow, attributed 18 percent of greenhouse gas emissions to livestock. A revised methodology in 2013, applying the same accounting framework used for other sectors, reduced this figure to approximately 14.5 percent.⁷

The nitrogen story is more nuanced. Smil notes that global nitrogen use efficiency (the share of applied fertilizer that ends up in harvested crop rather than escaping to air or water) averages around 40 percent globally, and has been falling in intensively farmed regions.¹ In China, over-fertilization has driven efficiency from 37 percent down to 29 percent, with the difference escaping as nitrous oxide (a potent greenhouse gas), ammonia (an air pollutant), and nitrates (which contaminate groundwater and create coastal dead zones).¹ This is a genuine problem with practical and affordable solutions: better timing of fertilizer application, matching fertilizer type to soil need, and precision agriculture technologies that reduce over-application.

The problems of industrial agriculture are, to a large extent, engineering problems. They have technical solutions that can be implemented incrementally, at scale, within existing agricultural systems. They do not require abandoning food production as we know it; they require improving it.

What “organic” actually means at scale

The appeal of organic farming as an environmental solution is real but its limits are underappreciated. A 2012 meta-analysis in Nature by Seufert and colleagues found that organic farming produces, on average, 25 percent lower yields than conventional farming across all crops, with the gap widening to 43 percent below conventional yields for some cereal crops.^x8 A subsequent 2017 analysis in Agronomy for Sustainable Development by Lesur-Dumoulin and colleagues examining more than 50 studies found yield gaps of 19 to 25 percent, with significant variation by crop and region.^x9

The implication is straightforward. Feeding the current global population on fully organic agriculture would require converting an additional 16 to 30 percent of the world’s remaining non-agricultural land to farmland, in order to compensate for lower yields.^x10 The biodiversity loss from that land conversion would likely exceed the biodiversity gains from reduced pesticide use on existing farmland. This does not make organic farming in any way bad, it simply makes it a context-specific tool instead of a global solution.

Smil notes that in the centuries before synthetic fertilizers, when all farming was “organic” by definition, 80 percent of people worked in farming, doing physically exhausting work for marginal returns. The “liberation” of the majority of humanity from agricultural labor, one of the most profound quality-of-life improvements in history, was made possible by the Haber-Bosch process, the synthesis of ammonia from atmospheric nitrogen, invented in 1913. Without synthetic nitrogen fertilizer, global crop yields would fall by roughly 40 to 50 percent, and roughly half of the current human population could not be fed on existing farmland.^x11

The alternatives don’t add up

Cultured meat: Promising, not a solution

The first cultured beef burger was produced in 2013 in the Netherlands at an estimated cost of $330,000.¹ By 2020, Singapore approved the first commercial sale of cultured chicken nuggets, produced by Eat Just, at a price point still far above commodity chicken. By 2021, total investment in the sector had reached approximately $2 billion.¹

The fundamental challenge is not biological but a matter of thermodynamics. Cultured meat production requires maintaining cells in a growth medium at controlled temperature and pH, with continuous oxygen supply, nutrient input, and waste removal. A 2023 preprint study by Risner and colleagues at UC Davis found that, under current production processes, the lifecycle greenhouse gas emissions of cultured beef could actually be higher than conventional beef over a 1,000-year time horizon, because the production of growth media requires large amounts of purified water and energy-intensive pharmaceutical-grade inputs.^x12

The energy demand is particularly problematic. A 2019 analysis in Frontiers in Sustainable Food Systems by Lynch and Pierrehumbert (Oxford) found that cultured meat’s climate advantage over cattle depends heavily on whether energy production is decarbonized. Because cultured meat emissions are almost entirely CO₂ (which accumulates indefinitely) rather than methane, which breaks down within a decade, the long-term warming impact of cultured meat can exceed that of cattle under scenarios of continued high consumption. The energy advantage of cultured meat over monogastrics (pigs and poultry) is marginal at best and may reverse under realistic production conditions.”¹³

None of this means cultured meat has no future. It may eventually serve specific markets, particularly as a supplement to conventional production in regions where land is extremely constrained. But Smil’s verdict is clear: it is currently “pilot scale” technology, commercially unproven at mass market pricing, and it cannot meaningfully contribute to feeding up to 10 billion people in the next two to three decades.¹

The vegan transition?

Beef is by far the largest emitter of CO₂ equivalent per kilogram of protein, compared to chicken or pork.¹⁴ A diet shift from beef to other proteins in high-income countries would measurably reduce the food system’s climate impact.

But Smil flags an important caveat that often goes unmentioned in advocacy for plant-based diets: mass adoption of veganism in wealthy countries, if it leads to increased consumption of out-of-season fruits, nuts, avocados, and specialty protein crops, may not reduce and could even increase total environmental pressure.¹ Almonds require approximately 12 liters of water per nut.¹⁵ Avocados, with their supply chains running from Mexico to Europe, have water footprints of approximately 320 liters per fruit and contribute to deforestation in growing regions.¹⁶

There is also a structural argument that rarely gets made: production animals serve functions beyond meat (and not even mentioning milk or eggs). Approximately 57 percent of current global livestock feed consists of materials that are not edible by humans: crop residues, grass from land unsuitable for cropping, and food processing byproducts such as oilseed cakes, bran, and distillers’ grains.¹⁷ Animals convert non-human-edible biomass into high-quality protein and fat. This is not waste but efficiency.

What Would Actually Work

First target waste

Global food waste amounts to approximately 1,000 kilocalories per person per day, roughly one-third of total food production.

The FAO estimates that approximately one-third of all food produced for human consumption, roughly 1.3 billion tons per year, is lost or wasted annually.¹⁸ Losses occur throughout the supply chain, from post-harvest spoilage in developing countries (where cold chain infrastructure is inadequate) to consumer behavior and retail overproduction in wealthy ones. The environmental cost of this waste is itself enormous: the production of food that is ultimately not eaten accounts for approximately 8 percent of global greenhouse gas emissions.¹⁹

The N fix that is already possible

Improving global nitrogen use efficiency (NUE) from its current 40 percent average to 60 to 65 percent, a target achievable through existing precision agriculture technologies (as mentioned before), would reduce the amount of synthetic nitrogen required to produce the current food output by roughly a third.²⁰ This single change would decrease nitrous oxide emissions (which are 273 times more potent than CO₂ over a 100-year timescale as a greenhouse gas, according to AR6, 2021 ²⁸), reduce freshwater nitrate contamination, and shrink coastal dead zones.

The technologies required are not exotic. Split nitrogen application (applying fertilizer in multiple smaller doses timed to crop uptake rather than one large dose at planting) can increase NUE by 15 to 20 percent with no change in yield.²¹ Soil testing and variable rate application technology, where GPS-guided equipment applies different fertilizer rates across a field based on measured soil nutrient levels, can improve NUE by a further 10 to 15 percent.²² These are available now, at commercially viable cost, for large-scale farming operations.

The barrier is not technical but rather economic and behavioral: fertilizer is cheap relative to its yield benefit, so farmers have limited financial incentive to apply it precisely. Policy tools, whether taxes on nitrogen over-application, payments for NUE improvements, or tighter limits on fertilizer application near waterways, could close this gap.

Meat mix and moderation

Smil estimates that approximately one-third of global cereal production and two-thirds of the US grain harvest are currently fed to animals.¹ Feedlot beef carries a feed conversion ratio of roughly 30 kilograms of feed per kilogram of edible product at the high end.¹ Poultry and pork convert feed to protein far more efficiently, and pasture-raised ruminants on land unsuitable for cropping represent a different calculation entirely.

The case for moderating high-end beef consumption in wealthy countries rests primarily on efficiency and emissions, not on the nutritional dispensability of meat as a food category. Meat, including beef, is a nutritionally dense and difficult-to-replicate protein source. It provides all essential amino acids in highly bioavailable form, along with heme iron, which is absorbed at rates of 15 to 35 percent compared to 2 to 20 percent for non-heme iron from plant sources, as well as zinc, vitamin B12, selenium, and conditionally essential compounds such as creatine and carnitine that are absent or negligible in unfortified plant foods.²⁹ For populations in low- and middle-income countries where protein deficiency, iron deficiency, and micronutrient gaps remain widespread public health problems, the argument for reducing meat consumption requires a different cost-benefit analysis than it does in the United States or Northern Europe, where the concern is overconsumption rather than inadequacy.

The appropriate policy lever for high-income countries is therefore not elimination of meat categories but a shift in the composition of meat consumption toward more efficient and lower-emissions sources (more poultry and pork, less feedlot beef) while maintaining total protein adequacy. This is consistent with both the environmental evidence and updated dietary guidelines in major consuming nations. A 2016 analysis by Springmann and colleagues at Oxford, published in PNAS, found that transitioning toward diets in line with standard dietary guidelines could reduce global mortality by 6 to 10 percent and food-related greenhouse gas emissions by 29 to 70 percent compared with a 2050 reference scenario. ³⁰ A subsequent 2018 modelling study by the same group in Nature confirmed that the dietary-guidelines scenario alone (without requiring full elimination of animal products) achieves a 29 percent reduction in food-related GHG emissions relative to projected baseline consumption.²³ The gains are concentrated in high-income countries, and the modelling explicitly notes that applying the same dietary shift logic to low-income countries would in several cases increase land and water use rather than reduce it.³¹

Smil’s preferred framing holds: the goal is meat moderation and mix optimization, not categorical elimination.

What happens to everything else if the food system fails?

The answer is: everything collapses. Food insecurity at scale produces predictable cascades: political instability, refugee flows, conflict over resources, public health crises, and the breakdown of governance institutions that depend on social legitimacy. The Arab Spring, which reshaped the politics of a continent (and arguably the world), was triggered in part by a global food price spike following the 2010 Russian wheat export ban and droughts in major grain-producing regions.³

By contrast, the collapse of the smartphone market, while economically painful, would likely not produce famine, mass migration, or state failure. The collapse of social media platforms, though consequential for public discourse, would not endanger human life. The collapse of the global financial system, as catastrophic as the 2008 crisis demonstrated it could be, is survivable in ways that the collapse of food production is not.

The world needs to feed 9.7 billion people in 2050, according to the UN medium-population projection.²⁴ The cultured meat industry cannot scale to meaningful market share within that timeframe under any realistic projection. Precision nitrogen management can, and is already beginning to, because it requires only incremental adoption of existing technology by existing farmers working existing land.

The nutritional transition that high-income countries have largely completed, from adequate calories to excess calories to dietary choice, is not yet available to much of the world’s population. Agricultural development policy that ignores this gradient would impose wealthy-world concerns on people or categories for whom adequate nutrition remains an unsolved problem.

Sustainability discourses must get priorities right

Food production is the prerequisite for everything else. Applying regulatory pressure to it without carefully calibrating the effects on output, price, and access is different in kind from applying regulatory pressure to other sectors. When a factory closes due to regulatory non-compliance, workers lose jobs and consumers pay more for a product. When a region’s agricultural capacity declines due to poorly designed policy, people go hungry.

The European Union’s Farm to Fork strategy, adopted in 2020, proposed reducing synthetic pesticide use by 50 percent and synthetic fertilizer use by 20 percent, while increasing organic farmland to 25 percent of total agricultural area, all by 2030.²⁵ These are admirable environmental goals. But a 2021 analysis by Beckman and colleagues at the USDA Economic Research Service found that full implementation of the Farm to Fork targets would reduce EU agricultural output by 7 to 12 percent and increase consumer food prices by 5 to 11 percent.²⁶ A JRC (Joint Research Centre of the European Commission) report from the same year found that global adoption of Farm to Fork-style policies would actually increase GHG emissions by up to 6 percent, because production displaced from Europe would move to regions with less efficient farming systems and weaker environmental controls.²⁷

Agricultural environmental policy is essential; so is designing it carefully, with quantitative impact assessment, realistic timelines, and protections for the most vulnerable consumers.

What actually reduces food system emissions

The research literature on food system decarbonization converges on a consistent set of effective interventions, none of which involve dismantling existing agricultural production:

Reducing food waste. A 30 percent reduction in food loss and waste globally would reduce food system GHG emissions by roughly 8 to 10 percent.¹⁹ This is achievable through infrastructure investment (cold chains in developing countries), behavioral change (consumer education in wealthy ones), and regulatory reform (relaxing cosmetic standards for produce that create waste at the retail level).

Sustainable diets in high-income countries with a smart mix of protein sources, including poultry, pork, legumes, and dairy. Agriculture systems, including livestock production, should indeed operate at the lowest emissions level possible and with reduced antibiotic use to protect the environment, animals, and ultimately humans.

Improving agricultural productivity in low-income countries, particularly sub-Saharan Africa. Smil notes that average nitrogen application rates in sub-Saharan Africa are approximately 3 kilograms per hectare, compared to 50 kilograms in China and 30 kilograms in Europe.¹ Increasing yields in Africa to levels achievable with modest fertilizer application and better seed varieties would allow the same food output from less land, reducing pressure on forests and biodiversity.

Improving nitrogen use efficiency in high-input farming systems through the technologies described earlier in the article.

None of these interventions require a technological revolution. They require investment, policy reform, and the political will to treat food production as the strategic priority it is.

References

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13. Lynch, J., & Pierrehumbert, R. (2019). Climate impacts of cultured meat and beef cattle. Frontiers in Sustainable Food Systems, 3, 5. https://doi.org/10.3389/fsufs.2019.00005

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16. Carrasco, L.R., Papworth, S.K., Reed, J., et al. (2017). High trade-offs between local and global demand for avocados. Nature Plants, 3, 1–3. See also Kibria, M.G., & Behrooz, M. (2022). Water footprint and environmental impact of avocado production. Sustainability, 14(2), 888.

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23. Springmann, M., Clark, M., Mason-D’Croz, D., Wiebe, K., Bodirsky, B.L., Lassaletta, L., de Vries, W., Vermeulen, S.J., Herrero, M., Carlson, K.M., Jonell, M., Troell, M., DeClerck, F., Gordon, L.J., Zurayk, R., Scarborough, P., Rayner, M., Loken, B., Fanzo, J., Godfray, H.C.J., Tilman, D., Rockstrom, J., & Willett, W. (2018). Options for keeping the food system within environmental limits. Nature, 562, 519–525. https://doi.org/10.1038/s41586-018-0594-0

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Antibiotic growth promoters (AGPs) have routinely been used in intensive poultry production for improving birds’ performance. However, in recent years, reducing the use of antibiotics in animal production has become a top priority, due to concerns about the development of antibiotic-resistant bacteria and mounting consumer pressure. Multiple countries have introduced bans or severe restrictions on the non-therapeutic use of antibiotics, including in the US, where the Food and Drug Administration has implemented measures to curb the use of antibiotics since 2017.

However, the removal of AGPs poses challenges for poultry performance, including reduced feed efficiency, decreased daily weight gain, as well as higher mortality. Moreover, the withdrawal of AGPs in feed is widely recognized as one of the predisposing factors for necrotic enteritis (NE). NE is one of the most common and economically important poultry diseases, with an estimated global impact of US$ 5 to 6 billion per year. As a result of withdrawing AGPs, the usage of therapeutic antibiotics to treat NE has increased. To break out of this vicious cycle and to secure the efficiency of poultry production, alternatives are needed that combat NE where it starts: in the gut.

Necrotic enteritis: a complex disease

NE is caused by pathogenic strains of Clostridium perfringens (CP): ubiquitous, gram-positive, spore-forming anaerobic bacteria. The spores of CP can be found in poultry litter, feces, soil, dust, and contaminated feed. Low levels of different CP strains are naturally present in the intestines of healthy birds, kept in check by a balanced microbiome. However, when gut health is compromised, pathogenic strains can proliferate at the expense of unproblematic strains, resulting in clinical or sub-clinical NE.

Animals suffering from the clinical form show symptoms such as general depression, reluctance to move, and diarrhea, with mortality rates of up to 50%. Infected birds suffer from degenerated mucosa lesions in the small intestines. Even in its “mild”, subclinical form, which often goes unnoticed, the damage to the animals’ intestinal mucosa can result in permanently reduced performance and consequent economic losses for the producer.

Certain predisposing factors have been found to enable the proliferation of pathogenic strains in the gastrointestinal tract. Diet is a key example: the composition of the gut flora is directly linked to feed composition. High inclusion rates of cereals (barley, rye, oats, and wheat) that contain high levels of non-starch polysaccharides (NSPs), high levels of indigestible protein, and inclusion of proteins of animal origin (e.g. fishmeal) have been shown to predispose birds to NE.

A range of diseases (e.g. chicken infectious anemia, Gumboro, and Marek’s disease), but also other factors that have immunosuppressive effects, such as heat or cold stress, mycotoxins, feed changes, or high stocking density, render birds more susceptible to intestinal infections. The single most prominent predisposing factor for the occurrence of NE is the mucosal damage caused by coccidiosis.

Gut health is key to combating necrotic enteritis

To control NE, a holistic approach to optimizing the intestinal health of poultry is needed. It should take into account not only parameters such as diet, hygiene, and stress, but should also make use of innovative tools.

Phytomolecules, also known as secondary plant compounds, are essentially plants’ defense mechanisms against pathogens such as moulds, yeasts, and bacteria. Studies have demonstrated the antimicrobial effects of certain phytomolecules, including against antibiotic-resistant pathogens. Phytomolecules have also been found to boost the production of digestive enzymes, to suppress pro-inflammatory prostaglandins and have antioxidant properties. These features make them a potent tool for optimizing gut health, potentially to the point of replacing AGPs.

Can phytomolecules mitigate the impact of necrotic enteritis?

To study the impact of phytomolecules on the performance of broilers challenged with a NE-causing CP strain, a trial was conducted at a US-based research facility. In this 42-day study, 1050 male day-old Cobb 500 broiler chicks were divided into 3 groups, with 7 replicates of 50 chicks each.

On the first day, all animals were vaccinated against coccidiosis through a live oocyst spray vaccination. The experimental diets met or exceeded the National Research Council requirements, and were fed as crumbles/pellets. On days 19, 20, and 21, all pens, except the negative control group, were challenged with a broth culture of C. perfringens. A field isolate of CP known to cause NE (originating from a commercial broiler operation) was utilized as the challenge organism. On day 21, three birds from each pen were selected, sacrificed, group weighed, and examined for the degree of present NE lesions.

The positive control group received no supplements. The trial group received a synergistic combination of two phytogenic products containing standardized amounts of selected, microencapsulated phytomolecules: an in-feed phytogenic premix (Activo^®, EW Nutrition GmbH) and a liquid complementary feed supplied via the drinking water (Activo® Liquid, EW Nutrition GmbH). The products were given at inclusion rates corresponding to the manufacturer’s baseline antibiotic reduction program recommendations (Figure 1):

Figure 1: Trial design

The trial results indicate that the addition of phytomolecules helps to mitigate the impact of NE on broilers’ performance. The group receiving Activo® and Activo® Liquid showed a better feed conversion (Figure 2) compared to the positive control group (NE challenge, no supplement). Also, better lesion scores were noted for animals receiving phytomolecules (0.7 and 1) than for the positive control group (1.6).

The most significant effect was observed concerning mortality: the group receiving Activo® and Activo® Liquid showed a 50% lower mortality rate than the positive control group (Figure 3). These results clearly indicate that phytomolecules can play an important role in mitigating losses due to NE.

Figure 1: Adjusted FCR

Figure 2: Lesion scores and mortality

Tackling necrotic enteritis in a sustainable way

In an age of AGP-free poultry production, a concerted focus on fostering animals’ gut health is key to achieving optimal performance. This study strongly demonstrates that, thanks to their antimicrobial, digestive, anti-inflammatory and antioxidant properties, phytomolecules effectively support birds’ intestinal health when challenged with NE. The inclusion of Activo® and Activo® Liquid, two phytogenic products designed to synergistically support birds during critical periods, resulted in improved feed conversion, better lesion scores, and 50% lower mortality.

In combination with good dietary, hygiene, and management practices, phytomolecules are therefore a potent tool for reducing the use of antibiotics: including Activo® and Activo® Liquid in their animals’ diets allows poultry producers to reduce the incidence of NE, to mitigate its economic impact in case of outbreaks, and therefore to control NE in a sustainable way.

By A. Bhoyar, T. van Gerwe and S. Regragui Mazili

References

Antonissen, Gunther, Siska Croubels, Frank Pasmans, Richard Ducatelle, Venessa Eeckhaut, Mathias Devreese, Marc Verlinden, Freddy Haesebrouck, Mia Eeckhout, Sarah De Saeger, Birgit Antlinger, Barbara Novak, An Martel, and Filip Van Immerseel. “Fumonisins Affect the Intestinal Microbial Homeostasis in Broiler Chickens, Predisposing to Necrotic Enteritis.” Veterinary Research 46, no. 1 (September 23, 2015): Article 98. doi:10.1186/s13567-015-0234-8.

Moore, Robert J. “Necrotic Enteritis Predisposing Factors in Broiler Chickens.” Avian Pathology 45, no. 3 (May 31, 2016): 275-81. doi:10.1080/03079457.2016.1150587.

Tang, Karen L., Niamh P. Caffrey, Diego B. Nóbrega, Susan C. Cork, Paul E. Ronksley, Herman W. Barkema, Alicia J. Polachek, Heather Ganshorn, Nishan Sharma, James D. Kellner, and William A. Ghali. “Restricting the Use of Antibiotics in Food-producing Animals and Its Associations with Antibiotic Resistance in Food-producing Animals and Human Beings: A Systematic Review and Meta-analysis.” The Lancet Planetary Health 1, no. 8 (November 6, 2017): 316-27. doi:10.1016/s2542-5196(17)30141-9.

Van Immerseel, Filip, Julian I. Rood, Robert J. Moore, and Richard W. Titball. “Rethinking Our Understanding of the Pathogenesis of Necrotic Enteritis in Chickens.” Trends in Microbiology 17, no. 1 (2009): 32-36. doi:10.1016/j.tim.2008.09.005.

Wade, Ben, and Anthony Keyburn. “The True Cost of Necrotic Enteritis.” PoultryWorld. October 09, 2015. Accessed August 19, 2019.

 Source Photo: Aviagen

by Ajay Bhoyar, Global Technical Manager, EW Nutrition

Anyone working with today’s fast-growing broiler chicken knows that it is a sensitive creature – and so is its gut health. Thanks to continuous improvements in terms of genetics and breeding, nutrition and feeding, as well as general management strategies, broiler production has tremendously upped performance and efficiency over the past decades. It is estimated that, between 1957 and 2005, the broiler growth rate increased by over 400%, while the feed conversion ratio dropped by 50%.

These impressive improvements, however, have come at the cost of intense pressure on the birds’ digestive system, which needs to process large quantities of feed in little time. To achieve optimal growth, a broiler’s gastrointestinal tract (GIT) needs to be in perfect health, all the time. Unsurprisingly, enteric diseases such as necrotic enteritis, which severely damages the intestinal mucosa, hamper the intestines’ capacity to absorb nutrients and induce an inflammatory immune response.

The modern broiler’s gut – a high-performing, but sensitive system

However, in a system as high performing as the modern broiler’s GIT, much less can lead to problems. From when they are day-old chicks up to slaughter, broilers go through several challenging phases during which they are more likely to show impaired gut functionality, e.g. after vaccinations or feed changes. Good management practices go a long way towards eliminating unnecessary stressors for the animals, but some challenging periods are unavoidable.

The transition from starter to grower diets is a classic situation when nutrients are very likely to not be well digested and build up in the gut, fueling the proliferation of harmful microbes. Immunosuppressive stress in combination with an immature intestinal microflora results in disturbances to the bacterial microbiota. At “best”, this entails temporarily reduce nutrient absorption, in the worst case the birds will suffer serious intestinal diseases.

Phytomolecules – the intelligent alternative to antibiotics

To safeguard performance during stressful periods, poultry producers need to anticipate them and proactively provide effective gut health support. For many years, this support came in the form of antibiotic growth promoters (AGP): administered prophylactically, they were effective at keeping harmful enteric bacteria in check. However, due to grave concerns about the development of antimicrobial resistance, non-therapeutic antibiotics use has been banned in many countries. Alternatives need to focus on improving feed digestibility and strengthening gut health, attacking the root causes of why the intestinal microflora would become unbalanced in the first place.

Phytomolecules are secondary metabolites active in the defense mechanisms of plants. Studies have found that certain phytomolecules stimulate digestive enzyme activities and stabilize the gut microflora, “leading to improved feed utilization and less exposure to growth-depressing disorders associated with digestion and metabolism” (Zhai et al., 2018). With other trials showing positive effects on broilers’ growth performance and feed conversion, the research indicates that phytomolecules might also specifically support chickens during challenging phases.

The effect of phytomolecules on broilers during a challenging phase

A study was conducted over a period of 49 days on a commercial broiler farm of an AGP-free integration operation in Japan. The farm reported gut health challenges in the second and third week of the fattening period due to vaccinations and changes to the animals’ diets. The trial included 15504 Ross 308 broilers, divided into two groups. The negative control group included a total of 7242 birds, kept in another house.

All the birds were fed the standard feed of the farm. The trial group (8262 birds) received Activo Liquid, which contains a synergistic combination of phytomolecules, administered directly through the drinking water. Activo Liquid was given at an inclusion rate of 200ml per 1000L of water (3.3 US fl oz per gallon of stock solution, diluted at 1:128), from day 8 until day 25, for 8 hours a day.

The results are summarized in Figure 1:

Figure 1: Improved broiler performance for Activo Liquid group (day 49)

The Activo Liquid group clearly showed performance improvements compared to the control group. Livability augmented by 1.5%, while the feed conversion rate improved by 3.2%. This resulted in a more than 5% higher score in terms of the performance index.

Challenging times? Tackle them using phytomolecules

Poultry producers take great care to eliminate unnecessary sources of stress for their birds. Nonetheless, during their lifecycle, broiler chickens face challenging periods during which the balance of the intestinal microflora can easily become disturbed, with consequences ranging from decreased nutrient absorption to full-blown enteric disease.

The trial reviewed here showed that, after receiving Activo Liquid, broilers raised without AGPs showed encouraging performance improvements during a challenging phase of feed changes and vaccinations. Likely thanks to the activation of digestive enzymes and a stabilization of the gut flora, the broilers showed improved livability and feed conversion, thus delivering a much more robust performance during a critical phase of their lives. In times where the non-therapeutic use of antibiotics is no longer an option, phytomolecules allow poultry farmers to effectively support their animals during challenging times.

References

Photo Source: Aviagen

Adedokun, Sunday A., and Opeyemi C. Olojede. “Optimizing Gastrointestinal Integrity in Poultry: The Role of Nutrients and Feed Additives.” Frontiers in Veterinary Science 5 (January 31, 2019): 348.

Jamroz, D., T. Wertelecki, M. Houszka, and C. Kamel. “Influence of Diet Type on the Inclusion of Plant Origin Active Substances on Morphological and Histochemical Characteristics of the Stomach and Jejunum Walls in Chicken.” Journal of Animal Physiology and Animal Nutrition 90, no. 5-6 (March 23, 2006): 255–68. 

Tavárez, Marcos A., and Fausto Solis De Los Santos. “Impact of Genetics and Breeding on Broiler Production Performance: a Look into the Past, Present, and Future of the Industry.” Animal Frontiers 6, no. 4 (October 1, 2016): 37–41.

Zhai, Hengxiao, Hong Liu, Shikui Wang, Jinlong Wu, and Anna-Maria Kluenter. “Potential of Essential Oils for Poultry and Pigs.” Animal Nutrition 4, no. 2 (June 2018): 179–86.

Zuidhof, M. J., B. L. Schneider, V. L. Carney, D. R. Korver, and F. E. Robinson. “Growth, Efficiency, and Yield of Commercial Broilers from 1957, 1978, and 20051.” Poultry Science 93, no. 12 (December 2014): 2970–82. 

Antimicrobial resistance (AMR) is a major threat to global public health. It is largely caused by the overuse of antibiotics in human medicine and agriculture. In intensive poultry production most antibiotics are used as antimicrobial growth promoters and/or used as prophylactic and metaphylactic treatments to healthy animals. Reducing such antibiotic interventions is crucial to lowering the incidence of AMR. However, antibiotic reduction often results in undesirable performance losses. Hence alternative solutions are needed to boost poultry performance. Phytomolecules have antimicrobial, digestive, anti-inflammatory and antioxidant properties, which could make them key to closing the performance gap.

Poultry performance depends on intestinal health

Poultry performance is to a large extent a function of intestinal health. The intestines process nutrients, electrolytes and water, produce mucin, secrete immunoglobulins and create a barrier against antigens and pathogens.

In addition, it is an important component of the body’s immune defense system. The intestine has to identify pathogens and reject them, but also has to tolerate harmless and beneficial microorganisms. If the intestines do not function properly this can lead to food intolerance, dysbiosis, infections and diseases. All of these are detrimental to feed conversion and therefore also to animal performance.

Antibiotics reduce the number of microorganisms in the intestinal tract. From a performance point of view this has two benefits: first, the number of pathogens is reduced and therefore also the likelihood of diseases; second, bacteria are eliminated as competitors for the available nutrients. However, the overuse of antibiotics not only engenders AMR: antibiotics also eliminate probiotic bacteria, which negatively impacts the digestive tracts’ microflora.

Products to boost poultry performance may be added to their feed or water. They range from pre- and probiotics to medium chain fatty acids and organic acids to plant extracts or phytomolecules. Especially the latter have the potential to substantially reduce the use of antibiotics in poultry farming.

Phytomolecules are promising tools for antibiotic reduction

Plants produce phytomolecules to fend off pathogens such as moulds, yeasts and bacteria. Their antimicrobial effect is achieved through a variety of complex mechanisms. Terpenoids and phenols, for example, disturb or destroy the pathogens’ cell wall. Other phytomolecules inhibit their growth by influencing their genetic material. Studies on broilers show that certain phytomolecules reduce the adhesion of pathogens such as to the wall of the intestine. Carvacrol and thymol were found to be effective against different species of Salmonella and Clostridium perfringens.

There is even evidence that secondary plant compounds also possess antimicrobial characteristics against antibiotic resistant pathogens. In-vitro trials with cinnamon oil, for example, showed antimicrobial effects against methicillin resistant Staphylococcus aureus, as well as against multiresistant E. coli, Klebsiella pneumoniae and Candida albicans.

Importantly, there are no known cases to date of bacteria developing resistances to phytomolecules. Moreover, phytomolecules increase the production and activity of digestive enzymes, they suppress the metabolism of pro-inflammatory prostaglandins and they act as antioxidants. Their properties thus make them a promising alternative to the non-therapeutic use of antibiotics.

Study design and results

In order to evaluate the effect of phytomolecules on poultry performance, multiple feeding studies were conducted on broilers and laying hens. They were given a phytogenic premix (Activo, EW Nutrition GmbH) that contains standardized  amounts of selected phytomolecules.

To achieve thermal stability during the feed processing and a targeted release in the birds’ gastrointestinal tract, the product is microencapsulated. For each , the studies evaluated both the tolerance of the premix and the efficacy of different dosages.

Study I: Evaluation of the dose dependent efficacy and tolerance of Activo for broilers
Animals:             400 broilers; age: 1-35 days of age
Feed:                  Basal starter and grower diets
Treatments:
– No supplement (negative control)
– 100 mg of Activo /kg of feed
– 1.000 mg of Activo /kg of feed
– 10.000 mg of Activo /kg of feed
Parameters:       weight gain, feed intake, feed conversion ratio, health status, and blood parameters

Results: The trial group given the diet supplemented with 100 mg/kg Activo showed significant improvements in body weight gain during the starter period (+4%) compared to the control group. Additional significant improvements in feed conversion ratio (FCR) in the growing period (+4%) resulted in an overall improvement in FCR of 3%. At a 1.000 mg/kg supplementation, a significant improvement in FCR of 6% was observed over the entire feeding period. Hematological parameters were within the reference range of healthy birds when feeding up to 10,000 Activo/ kg of feed.

Study II: Evaluation of the dose depending efficacy and tolerance of Activo for laying hens

Animals:             200 hens; age: 20 to 43 weeks
Feed:                  basal diet for laying hens
Treatments:
– No supplement (negative control)
– 100 mg of Activo/ kg of feed
– 250 mg of Activo/ kg of feed
– 500 mg of Activo/ kg of feed
– 5.000 mg of Activo/ kg of feed
Parameters:      weight gain, feed intake, feed conversion ratio, health status, and blood parameters

Results: Inclusion levels from 100 mg/kg of Activo onwards improved laying performance, egg mass and egg weight and reduced FCR compared to the control group. Results recorded for hematological parameters were within the reference range of healthy birds when feeding up to 5.000 mg Activo/ kg of feed.

Study III: Evaluation of the dose-dependent effects of Activo for coccidiosis vaccinated broilers

Animals:             960 broiler chickens; age: 42 days
Feed:                  Standard starter and finisher feed
Treatments:
– No supplement (negative control)
– 50 g of Activo /US ton of feed
– 100 g of Activo /US ton of feed
– 150 g of Activo /US ton of feed
– 200 g of Activo /US ton of feed
– 250 g of Activo /US ton of feed
– Antibiotic growth promoter (AGP)(positive control)
Parameters:      weight gain, feed efficiency
Specific:           In order to represent field conditions, the birds were challenged with used, homogenized litter.

Results: A clear dose response for both body weight gain and feed efficiency was observed (see Figure 1): the more phytogenic premix given, the better the birds’ performance. The group with 200g of Activo /US ton of feed showed similar performance levels than the positive control group supplemented with AGP.

Figure 1: Dose-dependent effects of for coccidiosis vaccinated broilers

Study IV:  Evaluation of the dose-dependent effects of Activo for laying hens

Animals:           40 hens; age: week 20 to 43
Feed:                basal diet for laying hens
Treatments:
– No supplement (negative control)
– 100 mg of Activo/ kg of feed
– 250 mg of Activo/ kg of feed
– 500 mg of Activo/ kg of feed
– 5.000 mg of Activo/ kg of feed
Parameters:      weight gain, feed intake, egg production, feed conversion ratio, health status
Duration:         168 days of feeding period

Results: The laying hens showed a higher laying rate when fed with a higher concentration of phytomolecules (Figure 2). Similarly improved results were observed for the feed efficiency. The more phytogenic premix added to their diet the better feed efficiency (Figure 3).

Figure 2: Dose-dependent effects of Activo on laying rate in laying hens

Figure 3: Dose-dependent effects of Activo on feed efficiency in laying hens

In conclusion, all four studies indicate that the inclusion of phytomolecules in broilers’ and laying hens’ diet improves their performance. Increasing levels of a phytogenic premix (Activo) significantly increased the production parameters for both groups. These improvements might bring performance in antibiotic-free poultry production on par with previous performance figures achieved with antimicrobial growth promoters.

The studies also showed that microencapsulated phytogenic premixes are safe when used in dose ranges recommended by the suppliers. No negative effects on animal health could be observed even at a 100 fold / 50 fold of the recommended inclusion rate in diets for broiler or laying hens, respectively. Thanks to their positive influence on intestinal health, phytomolecules thus boost poultry performance in a safe and effective way.

By Technical Team, EW Nutrition

Literature

Alanis, Alfonso J. “Resistance to Antibiotics: Are We in the Post-Antibiotic Era?” Archives of Medical Research 36, no. 6 (October 08, 2005): 697-705. doi:10.1016/j.arcmed.2005.06.009.

Borda-Molina, Daniel, Jana Seifert, and Amélia Camarinha-Silva. “Current Perspectives of the Chicken Gastrointestinal Tract and Its Microbiome.” Computational and Structural Biotechnology Journal 16 (March 15, 2018): 131-39. doi:10.1016/j.csbj.2018.03.002.

Diaz-Sanchez, Sandra, Doris Dsouza, Debrabrata Biswas, and Irene Hanning. “Botanical Alternatives to Antibiotics for Use in Organic Poultry Production.” Poultry Science 94, no. 6 (June 2015): 1419-430. doi:10.3382/ps/pev014.

Du, Encun, Weiwei Wang, Liping Gan, Zhui Li, Shuangshuang Guo, and Yuming Guo. “Effects of Thymol and Carvacrol Supplementation on Intestinal Integrity and Immune Responses of Broiler Chickens Challenged with Clostridium Perfringens.” Journal of Animal Science and Biotechnology 7, no. 19 (March 22, 2016). doi:10.1186/s40104-016-0079-7.

Gao, Pengfei, Chen Ma, Zheng Sun, Lifeng Wang, Shi Huang, Xiaoquan Su, Jian Xu, and Heping Zhang. “Feed-additive Probiotics Accelerate Yet Antibiotics Delay Intestinal Microbiota Maturation in Broiler Chicken.” Microbiome 5, no. 1 (August 03, 2017). doi:10.1186/s40168-017-0315-1.

Khan, Rosina, Barira Islam, Mohd Akram, Shazi Shakil, Anis Ahmad Ahmad, S. Manazir Ali, Mashiatullah Siddiqui, and Asad Khan. “Antimicrobial Activity of Five Herbal Extracts Against Multi Drug Resistant (MDR) Strains of Bacteria and Fungus of Clinical Origin.” Molecules 14, no. 2 (February 04, 2009): 586-97. doi:10.3390/molecules14020586.

Manafi, Milad, Mahdi Hedayati, Saeed Khalaji, and Mohammad Kamely. “Assessment of a Natural, Non-antibiotic Blend on Performance, Blood Biochemistry, Intestinal Microflora, and Morphology of Broilers Challenged with Escherichia Coli.” Revista Brasileira De Zootecnia 45, no. 12 (December 2016): 745-54. doi:10.1590/s1806-92902016001200003.

Photo source: Aviagen

Increased profitability in poultry production: EW Nutrition presents new comprehensive programs for the American market at Midwest Poultry Federation (MPF)
To support customers with effective solutions in animal production, EW Nutrition introduces the programs for Antibiotic Reduction and Toxin Risk Management in poultry. These programs contribute to solving the problem of antibiotic resistance by minimizing the input of antibiotics. In addition to innovative products the programs include customized consultancy services in the fields of animal nutrition, management and biosecurity.

At MPF, EW Nutrition will present new programs to reduce antibiotic use in broiler, broiler breeder and turkeys. A program to manage the toxin risk in poultry will also be introduced. One part of the programs is innovative products supporting gut and liver health and mitigating the impact of myco- and bacterial toxins. The other part is formed by consultancy services tailored to the particular needs of the customers.

The goals of the poultry programs are:

• stabilization of performance throughout the whole cycle
• constant high numbers of high quality chicks
• a reduced variety between flocks
• improved weight gain and feed conversion.

MARK RICHARDS, President of EW Nutrition USA

“Keeping performance high by simultaneously reducing the use of antibiotics is a balance act in animal production. We are convinced that the reduction of antibiotic use is the best way to reduce antibiotic resistance. With our comprehensive programs we support integrators, farmers and animals in coping with challenges occurring in animal production while increasing customers’ profitability.”

 EW Nutrition:

The customer-oriented company focusses on solving critical issues in animal nutrition by offering holistic and tailored programs for antibiotic reduction, toxin risk management and young animal nutrition. For this purpose EW Nutrition introduced innovative products and services resulting from solid R&D and business development. A global network of local commercial and technical support by experts guarantees the closeness to the customer. The reliable family-owned company is situated in Germany and has own R&D, production and application facilities in different parts of  the world.

Press contacts
EW Nutrition USA:   Mark Richards, mr@ew-nutrition.com

Animal plasma has been widely used in piglet feeding, not only as a protein source, but also as a tool to reduce gastrointestinal disorders after weaning.
Drs FELLIPE BARBOSA and INGE HEINZL* consider a safe alternative in order to keep animals healthy and to avoid loss of performance.

The recent developments surrounding the health risks associated with using animal plasma as a piglet feed ingredient is growing serious concerns in China. After the reported cases of African swine fever (ASF) commencing in August 2018, the Chinese government decided to ban the use of pig blood (and its by-products) in animal feed for some time.

The reason for the temporary ban of pig blood ingredients: African swine fever.
ASF is a viral disease of pigs and wild boars. The virus causes a lethal hemorrhagic disease in pigs. In some cases, the death of infected animals can occur during one week after the infection. There are no vaccines against the ASF Virus. When it hits the herd it is virtually impossible to stop its spread contaminating all animals.
Spreading of the virus occurs as follows:
• contact with contagious pigs from infected areas,
• contact with contaminated materials, being fed with kitchen waste and
• non-trusted animal origin feed ingredients.

There is a risk of pig blood carrying different types of viruses like ASF virus. Therefore, from time to time the use of ingredients based on blood is questioned by pig producers. To minimise this risk, the use of ingredients derived from pig slaughterhouses (including animal plasma) in pig feed is no longer allowed in China. This measure will cause not only a protein deficit in piglet feeds but also reduced protection of weaned piglets when intestinal disorders are concerned.

Immunoglobulins from animal plasma and its benefits on reducing post-weaning diarrhea (PWD)
The use of animal plasma has a positive effect on post-weaning performance of piglets. It is generally known that as a palatable ingredient, animal plasma stimulates feed intake. This results in better growth and a higher post-weaning performance in piglets. However, a closer inspection on the mode of action of spray dried plasma reveals its properties as an immune-ingredient and shows its supporting effect on the overall health status of the animals. Scientific publications showed that the positive influence on growth when feeding plasma to piglets is mainly due to its “immunoglobulin fraction”. This assigns to plasma a specific role in nutrition of weaned pigs to prevent PWD and to reduce the need for antibiotics.

Egg immunoglobulins: a natural way of protecting weaned piglets
Globigen® Jump Start (EW Nutrition GmbH) is a functional and standardized product based on whole egg powder. It contains natural immunoglobulins (IgY – “immunoglobulins from yolk”) mixed with a carrier. IgY are cells of the immune system from birds similar to the IgG in mammals. They have the main function of identifying and neutralizing harmful substances in the body. IgYs are obtained through a non-invasive process and are natural ingredients from eggs. There is no connection with blood and slaughter by-products and therefore no risk of carrying animal diseases.
Globigen® Jump Start is used to support piglets during critical stages of life, as long as their natural immunity is not completely developed. Scientific data confirmed that the IgY present in egg powder are capable of supporting intestinal health and growth performance of newly weaned piglets. More recently, also the possibility of using immunoglobulins as alternatives to zinc oxide (ZnO) and in-feed antibiotics (Hedegaard et al., 2017; Li at al. 2015) were evaluated with promising results.

Better results than plasma IgG: understanding the antigens causing post-weaning diarrhea
Animal plasma is a by-product of the meat industry. The animals slaughtered were possibly exposed to various diseases over their whole life. It cannot be considered as a standardized product in terms of immunoglobulins (either quantity nor quality). The Ig contained could be useful but also totally useless, depending on the pathogens the animals have been confronted with. As a source of immunoglobulins Globigen Jump Start is a costefficient and effective alternative to replace plasma in piglets’ diets. Its IgY content will have the same protection effect in the gut as IgG, but the nutritionist will have the possibility of choosing different protein sources in the market, either because of price or availability of raw materials. Our recommendation is that 40kg of plasma can be replaced by 2kg of Globigen Jump Start supplied with different high digestible protein sources.

A piglet trial was conducted with the objective of evaluate the efficacy of egg immunoglobulins on performance parameters of weaned piglets and to evaluate it as a substitute for animal plasma. Piglets were challenged with F4 and F18 entertoxic E. coli (ETEC) strains and feed either 2kg of Globigen Jump Start (GJS) or 40kg of spray dried plasma (SDP) in the weaner diet. The comparison was also done to a negative group (NG – microbiological challenge and no protection in the diet); and a positive group (PG – no microbiological challenge and antibiotics + ZnO in the diet).

Piglets from NG had lower feed intake, weight gain, and feed efficiency than animals from PG. The same was observed for piglets from GJS and SDP group. However, the impact of bacterial challenge on weight gain was lower for GJS piglets than for SDP (-14% and -52% when compared to PG); whereas feed intake was similar for both groups (-13% and -14% when compared to PG). The results showed that piglets receiving GJS where more efficient on converting feed into growth even when challenged when compared to SDP animals.

Trial conclusion
In this trial, the product based on egg immunoglobulins showed better influence on the performance of piglets than blood plasma. This may be due to the fact that the quality of the plasma depends on the animals slaughtered and on their contact with diseases, determining how much and which antibodies are available in this feed.
Additionally, blood plasma includes the danger of infectious diseases.

Safe and standard: free of swine related diseases and ruminant material
EW Nutrition clearly understands the importance of maintaining standardisation. It is a key factor for the customers to have a product that they can depend on every day.
Therefore, trough specific steps during the production of Globigen products, EW Nutrition ensures product quality. During production, all eggs are pasteurised and dried to a whole egg powder. In between steps include microbiological analysis, Salmonella, and avian disease controls to ensure the final product is free of the mentioned threats. Furthermore, as Globigen products are originated from laying hen farms there is no risk of contamination with any swine disease, like the devastating ASF. Finally, Globigen products do not contain any raw materials produced from, or substances derived from ruminants nor do the products come in contact with risk materials during the whole process (not be at risk for carrying transmissible spongiform encephalopathy or bovine spongiform encephalopathy – BSE).

ASIAN FEED MAGAZINE – February/March 2019

Another tool to reduce the use of antibiotics is the use of immunoglobulins from eggs.
Trials showed that this product is effective to support a calf’s start in life and also to offer support when challenged by various forms of diarrhoea.

The main cause for calf losses during the first two weeks of life is diarrhea. In general diarrhoea is characterised by more liquid being secreted than that being resorbed. However, diarrhoea is not a disease, but actually only a symptom. Diarrhea has a protective function for the animal, because the higher liquid volume in the gut increases motility and pathogens and toxins are excreted faster. Diarrhoea can occur for several reasons. It can be caused by incorrect nutrition, but also by pathogens such as bacteria, viruses and protozoa.

Bacteria in the gut
E. coli belong to the normal gut flora of humans and animals and can be mainly found in the colon. Only a fraction of the serotypes causes diseases. The pathogenicity of E.coli is linked to virulence factors. Decisive virulence factors are for example the fimbria used for the attachment to the gut wall and the bacteria’s ability to produce toxins.

Salmonella in general plays a secondary role in calf diarrhea, however, salmonellosis in cattle is a notifiable disease. Disease due to Clostridia is amongst the most expensive one in cattle farming globally. In herbivores, clostridia are part of the normal gastro-intestinal flora, only a few types can cause serious disease. In calves, Clostridium perfringens occurs with the different types A, C, and D. Rotaviruses are the most common viral pathogens causing diarrhoea in calves and lambs. They are mainly found at the age of 5 to 14 days. Coronaviruses normally attack calves at the age of 5 to 21 days. Cryptosporidium parvum is a protozoa and presumed to be the most common pathogen causing diarrhoea (prevalence up to more than 60 %) in calves.

Undigested feed and incorrect use of antibiotics
Plant raw materials (mainly soy products) are partly used in milk replacers as protein sources. These products contain carbohydrates, that cannot be digested by calves which can lead to diarrhea. The transition from milk to milk replacer can also be a reason.

An early application of tetracyclines and neomycin to young calves can lead to a change in the villi, malabsorption and therefore to slight diarrhoea. Longer therapies using high dosages of antibiotics can also lead to a bacterial superinfection of the gut. The problem is that in a disease situation, antibiotics are often used incorrectly. The use of antibiotics only makes sense when there is a bacterial diarrhea and not due to viruses, protozoa or poor feed management. To keep the use of antibiotics as low as possible, alternatives need to be considered.

Egg powder to add immunoglobulins
In order to achieve optimal results in calf rearing two approaches are possible. Firstly, the prophylaxis approach. This is the method of choice as diarrhoea can mostly be prevented. Therefore, it is necessary to supply the calf with the best possible equipment. As antibodies are one crucial but limiting factor in the colostrum of the “modern” cow, this gap needs to be minimised.  A study conducted in Germany in 2015 demonstrated that more than 50% of the new-born calves had a deficiency of immunoglobulins in the blood. Only 41% of the calves showed an adequate concentration of antibodies in the blood (>10 mg IgG/ml blood serum). Immunoglobulins contained in hen eggs (IgY) can partly compensate for poor colostrum quality and serve as a care package for young animals. A trial was conducted with an egg powder product* on a dairy farm (800 cows) in Brandenburg, Germany. In total 39 new-born calves were observed until weaning (65^th day of life). Before birth, the calves were already divided into control and trial group according to the lactation number of their mother cow. All calves were fed the same and received four litres of colostrum with ≥ 50 mg IgG /ml on the first day of life.

Control (n=20):            no additional supplementation
Trial group (n=19):      day 1 – 5: 100 g of the egg powder product per animal per day mixed into the colostrum or milk.

It was shown that the calves in the trial group showed a significantly higher (13%) weaning weight (105.74 kg compared to 93.45 kg in the control group) and 18%  higher average daily gain (999 g compared to 848 g in the control group) (Figure 1 and Figure 2).

Support during acute diarrhea
When diarrhea occurs, the calf has to be treated. So the second approach is to find the best and quickest solution. It is not always necessary to use antibiotics, as they do not work against virus or protozoa. Egg antibodies can be an answer when combined with electrolytes as the following trial shows. On a dairy farm (550 cows) in Germany a feeding trial with a product based on egg powder and electrolytes** was conducted from December 2017 to May 2018. Two groups of calves were used. Before birth the animals were allocated into the two groups according to the calving plan and were examined from day one until weaning (77^th day of life). All calves suffering from diarrhea (38 in total, 17 in the control and 21 in the trial group) were treated as follows:

Control (n=17):            Application of electrolytes
Trial group (n=21):      50 g of the egg powder and electrolytes product twice daily, stirred into the milk replacer until diarrhea stopped.

If the diarrhea did not stop or even got worse, the animals were treated with antibiotics. It was shown that in the control group the antibiotic treatment necessary was nearly twice as long as needed in the trial group (Figure 3). This means also that nearly twice the amount of antibiotics were used. This leads to the conclusion that calves in the trial group had an improved health status compared to calves in the control group. A further result from the improved health status was an increase in performance in the trial group (Figure 4).

The average daily weight gain of the trial group was 20% higher than in the control (600 vs. 500 g per day) leading to a significantly higher weaning weight (87.8 kg) than in the control (80.7 kg).

By Dr. Inge Heinzl, Editor EW Nutrition
Published in Dairy Global (Online and Printed), 10/2018

Breeding hens are a valuable asset for the poultry industry, as they produce the hatching eggs and day-old chicks. It is therefore important to manage contamination as well as possible. Mycotoxin management is part of that.

Egg production, however, is not the only parameter that is affected when breeding hens are exposed to mycotoxins. Earlier on in the reproductive cycle they already impact on embryonic mortality and hatchability. These effects are potentially more severe and may even occur without any noticeable change in the number of eggs produced.

Mycotoxins’ insidious consequences for eggshell quality and embryonic mortality

The eggshell is important to protect the progeny: thin and fragile shells can increase embryonic mortality, lower embryonic weight gain and decrease hatchability. Egg shell quality is a function of the hen’s calcium and vitamin D3 metabolism. The bioavailability of calcium and of vitamin D3 depends on intestinal integrity and on the production of enzymes and transporters that aid in feed metabolism. These processes can be adversely affected by aflatoxins, DON, T2, and Fumonisins.

The gastrointestinal tract is not the only site of mycotoxin action, however. Mycotoxins such as aflatoxins and ochratoxins have nephrotoxic effects, affecting calcium metabolism and increasing its excretion via the urine, while lowering its levels in blood serum.

Moreover, mycotoxins damage the liver, which plays a central role in egg production, being responsible for vitamin D3 metabolism and the synthesis of the lipids that make up the yolk. Moreover, the synthesis of transporters for lipids, calcium and carotenoids   ̶  important components of the egg  ̶  also takes place in liver. When liver function is impaired, the internal and external quality of the egg declines, which, in the end, affects the production of day-old chicks.

Figure 2 – Effects of mycotoxins on eggshell quality and embryonic mortality.

Figure 3 shows the effect of different mycotoxins on embryonic mortality. Incremental levels of ochratoxin or aflatoxin heighten embryonic mortality in a range from 1.5 to 7.5 times the embryonic mortality of the control group. In some cases, embryos are affected even when the hens received feed contaminated with mycotoxin levels that are within the guidelines suggested by the EFSA.

For example, an exposure to 4900ppb of DON for ten weeks increases the number of embryos with abnormalities. The causes are not entirely clear, as only traces of DON can be found in the egg. However, we do know that this mycotoxin can affect the protein synthesis at the level of the hen’s liver and therefore compromise the deposition of nutrients into the egg.

Mycotoxins’ effects on the progeny may cause long-term damage

Ochratoxin and aflatoxin can be transferred into the egg, where they exert toxicity on the embryos. This does not necessarily result in mortality. However, the chicks can suffer from a compromised immune function due to two reasons: lower transmission of antibodies from the hen and lower viability of the chickens’ immune cells, accompanied by a lower relative weight of the bursa of Fabricio and the thymus.

When both aflatoxin and ochratoxin are present in the feed, the effect on these parameters is synergistic. As a consequence of mycotoxin contamination, the animals’ immune response is impaired, which makes them more susceptible to infection. The final result could be an increased early chick mortality due to a higher incidence of bacterial and viral infections.

The transmission of other mycotoxins into the egg is minimal. While this means that a direct effect on the progeny is unlikely to occur, mycotoxin contamination still has a snowball effect: we have to consider the indirect effect of a lower deposition of nutrients on chick quality.

Prevention is key: mycotoxin risk management for breeder hens

The best approach to manage mycotoxin risk is to implement an integrated strategy that includes good crop and grain storing practices, regular raw material sampling and mycotoxin evaluation and analysis. Management tools (such as MasterRisk) can help to evaluate mycotoxin interactions and to choose the best strategy for dealing with specific mycotoxin challenges.

The results of mycotoxin analyses can be used to take decisions regarding the inclusion levels of raw materials and in choosing feed additives that counteract mycotoxins. Products based on plant extracts, yeast cell walls and clay minerals can help to stabilise a digestive system challenged by mycotoxins. They support the barrier function in the intestine, preventing the passage of mycotoxins into the bloodstream.

Phytomolecules are another piece of the puzzle: thanks to their antimicrobial, anti-inflammatory and antioxidant properties, they support liver function. This is particularly important for long-living animals prone to accumulating mycotoxins in their body tissues.

For a long time the “deleterious effects” of mycotoxins on breeder hens and “their repercussions on progeny health status and performance have not received from a scientific point of view as much attention”(Calini and Sirri, 2007) as they ought to have. However, now that the dangers of mycotoxins for breeder hens’ welfare, health and performance are better understood, it is clear that mycotoxin risk evaluation and management is central to successful poultry production.