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Beneficial microbial signals from alternative feed ingredients: a way to improve sustainability of broiler production?

Published: August 5, 2019
By: Filip Van Immerseel 1, Venessa Eeckhaut 1, Robert J. Moore 2, Mingan Choct 3 and Richard Ducatelle 1. / 1 Department of Pathology, Bacteriology and Avian Diseases, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium; 2 School of Science, RMIT University, Bundoora, Vic., Australia; 3 School of Environmental and Rural Science, University of New England, Armidale, NSW, Australia.
Summary

More sustainable broiler meat production can be facilitated by the increased use of cheap by-products and local crops as feed ingredients, while not affecting animal performance and intestinal health, or even improving intestinal health, so that antibiotic usage is further reduced. To achieve this, knowledge of the relationship between the taxonomic and functional microbiota composition and intestinal health is required. In addition, the relationship between the novel feed sources, the substrates present in these feed sources, and the breakdown by enzymes and microbial networks can be crucial, because this can form the basis for development of tailored feed-type specific solutions for optimal digestion and animal performance.

Chicken meat production is more sustainable and has lower environmental impact than porcine and bovine meat production. Chicken production uses less feed consumed for each kilogram of meat produced and uses less land and water for both farming and feed production (Flachowsky et al., 2017). Moreover, the broiler production industry has, for many years, continuously improved animal performance, reflected by ever decreasing feed conversion (kg feed consumed per kg body weight) and reduced time to achieve market weight (Zuidhof et al., 2014). This helps reducing the carbon footprint. Drivers for the continuous improvements in performance parameters include genetic selection for high-performing chicken lines, technological developments in hatching and housing conditions, feed optimization and management practices that support (intestinal) health. Among the latter, the use of antimicrobial growth promoters (antimicrobials added to the diet at low concentrations) is a practice that has been stopped in the EU since 2006, but the use of therapeutic antimicrobials in the animal production industries is still high (Chantziaras et al., 2014; Diarra and Malouin, 2014; Van Boeckel et al., 2015). Because of concerns about antibiotic resistance and driven by legislation and consumers’ perception and demands, nowadays the use of antimicrobials is decreasing, in some cases leading to an increase in intestinal health problems.
The move away from antimicrobials has led to increasing concerns about gut health that may be compromised by bacterial diseases, enteritis, dysbiosis and poor digestibility and result in poor growth performance of birds. To overcome the increased incidence of gut health problems in animals, many different strategies have been developed. Often feed and drinking water additives are used. These include enzymes (mostly xylanases and glucanases), probiotics, short- and medium-chain fatty acids, herbal compounds, prebiotics and combinations of these, among other molecules (Huyghebaert et al., 2011; Caly et al., 2015; Gadde et al., 2017). In addition, research on the modes of action of these products and on underlying microbiota- or host-related functions involved in intestinal health has led to a better understanding of the intestinal ecosystem in health and disease (Stanley et al., 2014).
In production animals, a key issue is digestibility of nutrients and energy harvest from the diet. Although brush border enzymes and exogenous enzymes (in diet) are important in this regard, the gut microbiota has a key function in carbohydrate, fat and protein digestion as well (Flint et al., 2012; Scott et al., 2013). In case of incomplete digestion of nutrients in the small intestine, the excess nutrients from an energy-rich diet can fuel small intestinal bacterial overgrowth, potentially resulting in inflammation and in some case even severe disease (e.g. necrotic enteritis by Clostridium perfringens) (Shojadoost et al., 2012; Kiarie et al., 2013; Pan and Yu, 2014; Wu et al., 2014). To avoid such problems, different feed additives have been used to support host digestive processes. Exogenously added enzymes play a role and have been administered for many years as feed additives to enhance digestion (Amerah et al., 2017; Gonzalez-Ortiz et al., 2017).
Different feed ingredients are used in poultry diets in different regions around the world, with wheat and corn the most predominant cereals, and soya the most important protein source. Substituting (partly) these high-quality feed ingredients with alternative feed materials, often by-products from other industries or local products, could be a valuable way to further enhance sustainability of poultry production worldwide. Such alternative feed sources are often cheaper but may be less digestible, so animal performance can be reduced and the incidence of gut health problems can increase. Examples of alternative feed sources include distiller’s dried grains with solubles (DDGS), sunflower cake meal, cassava pulp, palm kernel cake/meal, lupines, sweet potatoes, insects, worms, seaweed and many others, often depending on local availabilities (Ravindran, 2013). Improving the digestibility of poorly digestible ingredients is a valuable objective where microbial biotechnological solutions can fill a need. Complex indigestible substrates, such as plant cell wall polysaccharides, require several enzymatic reactions in cascade in order to achieve full catabolism. The microbiota can break down these complex molecules, to an extent, and thus harvest energy that can, at least partly, be used by the host. In this process, microbial networks are essential, as different steps in complex substrate breakdown involve different bacterial taxa, with their specific enzymes, each participating in a certain step or process depending on the type of substrate present (Flint et al., 2012, 2015; White et al., 2014). Not only breakdown of substrates but also the end metabolic products that are produced during fermentation are of utmost importance, as these metabolites, for example short-chain fatty acids, steer intestinal health (Russell et al., 2013; Zhang and Davies, 2016). Microbial biotechnology can be of use in different disciplines that can contribute to more sustainable poultry (and other animal species) production in the future:
1) Defining the microbiota composition and microbial functional pathways in the chicken’s intestinal tract and their relation with intestinal health and performance.
Insight in microbial community organization and characterization of the functional activities of these communities is a key topic nowadays and essential to understand how microbiota–host interactions drive intestinal health and function. While some work has been done on describing microbiota composition in the different segments of the intestinal tract of chickens (Oakley et al., 2014; Antonissen et al., 2016; Stanley et al., 2016), there is a clear need to further investigate microbial taxa that are over- or underrepresented in the gut of chickens in specific experimentally induced or field cases of intestinal health problems. Even then, it will be of importance to evaluate the significance and possible causal relationships of these findings, as data derived from 16S rRNA sequencing are descriptive and do not necessarily reflect functionally and pathologically relevant changes. As an example, isolating and evaluating the behaviour of specific species in intestinal health models or studying their behaviour in vitro (e.g. substrate preference, metabolite production) can be valuable (De Maesschalck et al., 2015; Eeckhaut et al., 2016). Even more, future studies should target pathways present in the microbiota, as can be done using metagenomic approaches. This can add information on the functionality of a microbiota that is linked with intestinal health, and ideally, with performance.
A particular challenge in determining the contribution of gut microbiota to poultry productivity is understanding the metabolic potential and role of species within the microbiota that have not been cultured and characterized. 16S rRNA sequencing has shown that there are typically many members of the broiler gut microbiota that are only distantly related to strains that have currently been characterized. There are new culturing methods now available which may capture some of these unknown strains (Browne et al., 2016) and there are also advanced metagenomic sequence assembly methods that have been successfully used to construct whole genomes of novel organisms within the microbiota (Sangwan et al., 2016). There are great opportunities to apply these advanced microbiological methods to the chicken microbiota in order to improve our understanding of how the microbiota may influence the utilization of novel feed inputs.
2) Defining metabolic profiles in the gut and their relation with intestinal health.
While 16S rRNA sequencing and metagenomics can yield information on abundances of taxa and abundances of genes encoding functional activities, including DNA biomarker estimation (Segata et al., 2011), information on gene expression but especially on microbial metabolic profiles in the intestine will be essential to understand microbiota–host interplay in the gut. Products from polysaccharide fermentation (mainly lactate, shortchain fatty acids and gases) have been well studied in relation to intestinal health (Havenaar, 2011; Russell et al., 2013; Onrust et al., 2015). This is not the case for products from protein and fat degradation, although beneficial effects of, for example, indole, which is formed during degradation of tryptophan, are well described. More in-depth studies on the relationship between feed sources, their constituents and the microbial taxa that degrade these substrates, the microbial end-products and their dependence on the microbiota composition itself, are key targets for future research. This will enable moves towards optimal intestinal health using nutritional approaches. Ideally, besides the production of enzymes or other actions, probiotics could be designed to produce a set of microbial signals that reduce inflammation, inhibit pathogen overgrowth and favour digestion when delivered in-feed together with its substrates. The use of a complex of probiotic strains, which operate as a network to feed each other or produce different agonistic end metabolites, should be considered. Butyrate production is the most well-known example of a beneficial endproduct (Onrust et al., 2015).
3) Identifying enzymes and enzymatic degradation pathways needed to break down novel feed sources and application of tailored solutions for specific feed types
Enzymes have been used as feed additives in poultry diets for many years. Their main target so far was to reduce viscosity and decrease the levels of the so-called antinutritional compounds (Kiarie et al., 2013). A lot of these viscous compounds are soluble non-starch polysaccharides (NSPs, e.g. pectins, arabinoxylans and beta-glucans), typically present at high concentrations in specific feed ingredients (e.g. rye, barley and wheat; Knudsen, 2014). These NSPs are very complex because they can differ in molecular weight, side-chain length and composition, linkage types between molecules, and many more (Knudsen, 2014). The substrates are very heterogeneous, even within the same type of compounds (e.g. arabinoxylans), and thus, the enzymes needed to be tailored for these substrates in order to degrade them. Here, the challenge for microbial biotechnology is evident: first, there is a definite need to characterize, in detail, the composition of feed ingredients that can potentially replace high-quality cereals and soya; second, there is a strong need to identify enzymes (or mixes of them) that are capable of degrading these specific substrates. In this way, a feed-specific enzyme mixture could be designed and supplemented when specific sustainable feed ingredients are used to, at least partly, replace conventional cereals and protein sources in feed. Furthermore, there is an opportunity to develop microbial mixtures that form a substrate-degradation product of end metabolites beneficial for intestinal health. Thus, mass-scale stable production of these mixtures is a biotechnological challenge. All these above-mentioned ideas need coordinated approaches that combine classical microbiology, analytical chemistry, but also high-throughput sequencing and bioinformatics.
Summarizing, more sustainable broiler meat production can be facilitated by the increased use of cheap by-products and local crops as feed ingredients, while not affecting animal performance and intestinal health, or even improving intestinal health, so that antibiotic usage is further reduced. Therefore, knowledge of the relationship between the taxonomic and functional microbiota composition and intestinal health is required, and the relationship between the feed sources, the substrates present, and the breakdown by enzymes and microbial networks can be crucial, because this can form the basis for development of tailored feed-type specific solutions for optimal digestion and animal performance.
 
Conflict of interest
The authors declare that there is no conflict of interest.
 
This article was originally published in Microbial Biotechnology (2017) 10(5), 1008–1011 doi:10.1111/1751-7915.12794. This is an Open Access article under the terms of the Creative Commons Attribution License.

Amerah, A.M., Romero, L.F., Awati, A., and Ravindran, V. (2017) Effect of exogenous xylanase, amylase, and protease as single or combined activities on nutrient digestibility and growth performance of broilers fed corn/ soy diets. Poult Sci 96: 807–816.

Antonissen, G., Eeckhaut, V., Van Driessche, K., Onrust, L., Haesebrouck, F., Ducatelle, R., Moore, R.J., and Van Immerseel, F. (2016) Microbial shifts associated with necrotic enteritis. Avian Pathol 45: 308–312.

Browne, H.P., Forster, S.C., Anonye, B.O., Kumar, N., Neville, B.A., Stares, M.D., Goulding, D., and Lawley, T.D. (2016) Culturing of ‘unculturable’ human microbiota reveals novel taxa and extensive sporulation. Nature 533: 543–546.

Caly, D.L., D’Inca, R., Auclair, E., and Drider, D. (2015) Alternatives to antibiotics to prevent necrotic enteritis in broiler chickens: a microbiologist’s perspective. Front Microbiol 6: 1336.

Chantziaras, I., Boyen, F., Callens, B., and Dewulf, J. (2014) Correlation between veterinary antimicrobial use and antimicrobial resistance in food-producing animals: a report on seven countries. J Antimicrob Chemother 69: 827–834.

De Maesschalck, C., Eeckhaut, V., Maertens, L., De Lange, L., Marchal, L., Nezer, et al. (2015) Effects of xylo-oligosaccharides on broiler chicken performance and microbiota. Appl Environ Microbiol 81: 5880–5888.

Diarra, M.S., and Malouin, F. (2014) Antibiotics in Canadian poultry productions and anticipated alternatives. Front Microbiol 5: 282.

Eeckhaut, V., Wang, J., Van Parys, A., Haesebrouck, F., Joossens, M., Falony, G., et al. (2016) The probiotic butyricicoccus pullicaecorum reduces feed conversion and protects from potentially harmful intestinal microorganisms and necrotic enteritis in broilers. Front Microbiol 7: 1416.

Flachowsky, G., Meyer, U., and Sudekum, K.H. (2017) Land use for edible protein of animal origin-a review. Animals (Basel) 7. pii: E25. doi: 10.3390/ani7030025.

Flint, H., Scott, K., Duncan, S., Louis, P., and Forano, E. (2012) Microbial degradation of complex carbohydrates in the gut. Gut Microbes 3: 289–306.

Flint, H.J., Duncan, S.H., Scott, K.P., and Louis, P. (2015) Links between diet, gut microbiota composition and gut metabolism. Proc Nutr Soc 74: 13–22.

Gadde, U., Kim, W.H., Oh, S.T., and Lillehoj, H.S. (2017) Alternatives to antibiotics for maximizing growth performance and feed efficiency in poultry: a review. Anim Health Res Rev [Epub ahead of print] doi: 10.1017/ S1466252316000207.

Gonzalez-Ortiz, G., Sola-Oriol, D., Martinez-Mora, M., Perez, J.F., and Bedford, M.R. (2017) Response of broiler chickens fed wheat-based diets to xylanase supplementation. Poult Sci [Epub ahead of print] doi: 10.3382/ps/pex092.

Havenaar, R. (2011) Intestinal health functions of colonic microbial metabolites: a review. Benef Microbes 2: 103–114.

Huyghebaert, G., Ducatelle, R., and Van Immerseel, F. (2011) An update on alternatives to antimicrobial growth promoters for broilers. Vet J 187: 182–188.

Kiarie, E., Romero, L.F., and Nyachoti, C.M. (2013) The role of added feed enzymes in promoting gut health in swine and poultry. Nutr Res Rev 26: 71–88.

Knudsen, K.E. (2014) Fiber and nonstarch polysaccharide content and variation in common crops used in broiler diets. Poult Sci 93: 2380–2393.

Oakley, B.B., Lillehoj, H.S., Kogut, M.H., Kim, W.K., Maurer, J.J., Pedroso, A., et al. (2014) The chicken gastrointestinal microbiome. FEMS Microbiol Lett 360: 100–112.

Onrust, L., Ducatelle, R., Van Driessche, K., De Maesschalck, C., Vermeulen, K., Haesebrouck, F., Eeckhaut, V., and Van Immerseel, F. (2015) Steering endogenous butyrate production in the intestinal tract of broilers as a tool to improve gut health. Front Vet Sci 2: 75.

Pan, D., and Yu, Z. (2014) Intestinal microbiome of poultry and its interaction with host and diet. Gut Microbes 5: 108–119.

Ravindran, V. (2013) Poultry feed availability and nutrition in developing countries. Rome, Italy: FAO, pp. 67–69. http:// www.fao.org/3/a-al706e.pdf

Russell, W.R., Hoyles, L., Flint, H.J., and Dumas, M.E. (2013) Colonic bacterial metabolites and human health. Curr Opin Microbiol 16: 246–254.

Sangwan, N., Xia, F., and Gilbert, J.A. (2016) Recovering complete and draft population genomes from metagenome datasets. Microbiome 4: 8.

Scott, K.P., Gratz, S.W., Sheridan, P.O., Flint, H.J., and Duncan, S.H. (2013) The influence of diet on the gut microbiota. Pharmacol Res 69: 52–60.

Segata, N., Izard, J., Waldron, L., Gevers, D., Miropolsky, L., Garrett, W.S., and Huttenhower, C. (2011) Metagenomic biomarker discovery and explanation. Genome Biol 12: R60.

Shojadoost, B., Vince, A.R., and Prescott, J.F. (2012) The successful experimental induction of necrotic enteritis in chickens by Clostridium perfringens: a critical review. Vet Res 43: 74.

Stanley, D., Hughes, R.J., and Moore, R.J. (2014) Microbiota of the chicken gastrointestinal tract: influence on health, productivity and disease. Appl Microbiol Biotechnol 98: 4301–4310.

Stanley, D., Hughes, R.J., Geier, M.S., and Moore, R.J. (2016) Bacteria within the gastrointestinal tract microbiota correlated with improved growth and feed conversion: challenges presented for the identification of performance enhancing probiotic bacteria. Front Microbiol 7: 187.

Van Boeckel, T.P., Brower, C., Gilbert, M., Grenfell, B.T., Levina, S.A., and Robinson, T.P. (2015) Global trends in antimicrobial use in food animals. Proc Natl Acad Sci USA 112: 5649–5654.

White, B.A., Lamed, R., Bayer, E.A., and Flint, H.J. (2014) Biomass utilization by gut microbiomes. Annu Rev Microbiol 68: 279–296.

Wu, S.B., Stanley, D., Rodgers, N., Swick, R.A., and Moore, R.J. (2014) Two necrotic enteritis predisposing factors, dietary fishmeal and Eimeria infection, induce large changes in the caecal microbiota of broiler chickens. Vet Microbiol 169: 188–197.

Zhang, L.S., and Davies, S.S. (2016) Microbial metabolism of dietary components to bioactive metabolites: opportunities for new therapeutic interventions. Genome Med 8: 46.

Zuidhof, M.J., Schneider, B.L., Carney, V.L., Korver, D.R., and Robinson, F.E. (2014) Growth, efficiency, and yield of commercial broilers from 1957, 1978, and 2005. Poult Sci 93: 2970–2982.

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Authors:
Filip Van Immerseel
Ghent University
Ghent University
Venessa Eeckhaut
Ghent University
Ghent University
Professor Robert Moore
RMIT University
Mingan Choct
University of New England
University of New England
Richard Ducatelle
Ghent University
Ghent University
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dan hofer
7 de septiembre de 2019

Has anybody ever fed peas extruded at 300 Fahrenheit being heat extruded? I think it would be like eating raw potato versus french fries.

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Lawal Sesan
15 de julio de 2020

There are lots of alternative feed ingredients that have not been put into use, especially in Africa, but with the use of beneficial microbes a lot of them can be detoxified and used.

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Asaad Ahmed Elsabbagh
25 de marzo de 2020

This is a very nice and attractive article but i think it will take a long time to reach to the point that we can know the total microbiota composition and the specific function of each one or group, also to know the end product of each, the synergy or antagonist action between each other. So I think we have to depend on the advanced meta-genomic sequence assembly methods, which can allow us to more understanding the intestinal microbiota composition, grouping , functions, end products and its effects over the different digestibility, gut health and total performance markers.

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