Register      Login
Animal Production Science Animal Production Science Society
Food, fibre and pharmaceuticals from animals
REVIEW (Open Access)

Advances in prebiotics for poultry: role of the caeca and oligosaccharides

Natalie K. Morgan https://orcid.org/0000-0002-9663-2365 A *
+ Author Affiliations
- Author Affiliations

A Curtin University, School of Molecular and Life Sciences, Kent Street, Bentley, WA 6102, Australia.

* Correspondence to: natalie.morgan@curtin.edu.au

Handling Editor: David Masters

Animal Production Science 63(18) 1911-1925 https://doi.org/10.1071/AN23011
Submitted: 9 January 2023  Accepted: 6 March 2023   Published: 30 March 2023

© 2023 The Author(s) (or their employer(s)). Published by CSIRO Publishing. This is an open access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND)

Abstract

Prebiotics are non-digestible carbohydrates that selectively stimulate the growth of beneficial bacteria. Prebiotic supplementation into poultry diets results in a decreased rate of pathogenic bacteria colonisation in the gastrointestinal tract. It also enhances production of volatile fatty acids and lactic acid, which provide the bird with energy. This results in improved host gastrointestinal health and productive performance. Oligosaccharides are the most notable prebiotics in poultry nutrition. Examples of prebiotic oligosaccharides include xylo-oligosaccharides, fructo-oligosaccharides, and galacto-oligosaccharides. Oligosaccharides are derived from hydrolysis of non-starch polysaccharides (NSP). They are manufactured from plant sources, synthesised by physiochemical methods or enzymatic processes. The effects of oligosaccharides occur primarily in the caeca; oligosaccharides bypass the small intestine and reach the caeca, where they are readily fermented by beneficial bacteria, such as those in family Lactobacillaceae and Bifidobacteriaceae. Caeca function is generally poorly understood, despite extensive reviews and studies in this field. A deeper understanding of the factors that influence ability of the caeca to effectively utilise oligosaccharides is warranted. This would allow new prebiotic products and NSP- degrading enzymes to be developed, targeted to specific diets and scenarios. This is required, given the lack of consistency observed in the outputs derived from different studies assessing oligosaccharide efficacy in poultry diets. A key hinderance to progression in this field is that authors rarely analyse the oligosaccharide content and composition in the test diets and products, or in the bird’s gastrointestinal tract. This review examines the mechanisms behind how oligosaccharides induce prebiotic effects in poultry, by identifying the role of the caeca in NSP digestion and identifying the impact of oligosaccharides on caeca microbiota and short-chain fatty acid composition.

Keywords: caeca, enzymes, fibre, microbiota, non-starch polysaccharides, oligosaccharides, poultry, prebiotic, short-chain fatty acids.


References

Aachary AA, Prapulla SG (2011) Xylooligosaccharides (XOS) as an emerging prebiotic: microbial synthesis, utilization, structural characterization, bioactive properties, and applications. Comprehensive Reviews in Food Science and Food Safety 10, 2–16.
Xylooligosaccharides (XOS) as an emerging prebiotic: microbial synthesis, utilization, structural characterization, bioactive properties, and applications.Crossref | GoogleScholarGoogle Scholar |

Abd El-Hack ME, El-Saadony MT, Shafi ME, Qattan SYA, Batiha GE, Khafaga AF, Abdel-Moneim A-ME, Alagawany M (2020) Probiotics in poultry feed: a comprehensive review. Journal of Animal Physiology and Animal Nutrition 104, 1835–1850.
Probiotics in poultry feed: a comprehensive review.Crossref | GoogleScholarGoogle Scholar |

Abdallah AG, Beshara MM (2015) Effect of different levels and sources of dietary fibre on productive and economic performance in local laying hens during growing period and subsequent laying performance. Egyptian Poultry Science Journal 35, 367–398.

Adhikari P, Cosby DE, Cox NA, Franca MS, Williams SM, Gogal RM, Ritz CW, Kim WK (2018) Effect of dietary fructooligosaccharide supplementation on internal organs Salmonella colonization, immune response, ileal morphology, and ileal immunohistochemistry in laying hens challenged with Salmonella enteritidis. Poultry Science 97, 2525–2533.
Effect of dietary fructooligosaccharide supplementation on internal organs Salmonella colonization, immune response, ileal morphology, and ileal immunohistochemistry in laying hens challenged with Salmonella enteritidis.Crossref | GoogleScholarGoogle Scholar |

Akbaryan M, Mahdavi A, Jebelli-Javan A, Staji H, Darabighane B (2019) A comparison of the effects of resistant starch, fructooligosaccharide, and zinc bacitracin on cecal short-chain fatty acids, cecal microflora, intestinal morphology, and antibody titer against Newcastle disease virus in broilers. Comparative Clinical Pathology 28, 661–667.
A comparison of the effects of resistant starch, fructooligosaccharide, and zinc bacitracin on cecal short-chain fatty acids, cecal microflora, intestinal morphology, and antibody titer against Newcastle disease virus in broilers.Crossref | GoogleScholarGoogle Scholar |

Apajalahti J, Vienola K (2016) Interaction between chicken intestinal microbiota and protein digestion. Animal Feed Science and Technology 221, 323–330.
Interaction between chicken intestinal microbiota and protein digestion.Crossref | GoogleScholarGoogle Scholar |

Apajalahti JHA, Kettunen A, Bedford MR, Holben WE (2001) Percent G+C profiling accurately reveals diet-related differences in the gastrointestinal microbial community of broiler chickens. Applied and Environmental Microbiology 67, 5656–5667.
Percent G+C profiling accurately reveals diet-related differences in the gastrointestinal microbial community of broiler chickens.Crossref | GoogleScholarGoogle Scholar |

Asare PT, Greppi A, Pennacchia A, Brenig K, Geirnaert A, Schwab C, Stephan R, Lacroix C (2021) In vitro modeling of chicken cecal microbiota ecology and metabolism using the PolyFermS platform. Frontiers in Microbiology 12,
In vitro modeling of chicken cecal microbiota ecology and metabolism using the PolyFermS platform.Crossref | GoogleScholarGoogle Scholar |

Ayman U, Akter L, Islam R, Bhakta S, Rahman MA, Islam MR, Sultana N, Sharif A, Jahan MR, Rahman MS, Haque Z (2022) Dietary chitosan oligosaccharides improves health status in broilers for safe poultry meat production. Annals of Agricultural Sciences 67, 90–98.
Dietary chitosan oligosaccharides improves health status in broilers for safe poultry meat production.Crossref | GoogleScholarGoogle Scholar |

Ballou AL, Ali RA, Mendoza MA, Ellis JC, Hassan HM, Croom WJ, Koci MD (2016) Development of the chick microbiome: how early exposure influences future microbial diversity. Frontiers in Veterinary Science 3,
Development of the chick microbiome: how early exposure influences future microbial diversity.Crossref | GoogleScholarGoogle Scholar |

Baurhoo B, Phillip L, Ruiz-Feria CA (2007) Effects of purified lignin and mannan oligosaccharides on intestinal integrity and microbial populations in the ceca and litter of broiler chickens. Poultry Science 86, 1070–1078.
Effects of purified lignin and mannan oligosaccharides on intestinal integrity and microbial populations in the ceca and litter of broiler chickens.Crossref | GoogleScholarGoogle Scholar |

Bautil A, Verspreet J, Buyse J, Goos P, Bedford MR, Courtin CM (2019) Age-related arabinoxylan hydrolysis and fermentation in the gastrointestinal tract of broilers fed wheat-based diets. Poultry Science 98, 4606–4621.
Age-related arabinoxylan hydrolysis and fermentation in the gastrointestinal tract of broilers fed wheat-based diets.Crossref | GoogleScholarGoogle Scholar |

Bautil A, Verspreet J, Buyse J, Goos P, Bedford MR, Courtin CM (2020) Arabinoxylan-oligosaccharides kick-start arabinoxylan digestion in the aging broiler. Poultry Science 99, 2555–2565.
Arabinoxylan-oligosaccharides kick-start arabinoxylan digestion in the aging broiler.Crossref | GoogleScholarGoogle Scholar |

Bautil A, Buyse J, Goos P, Bedford MR, Courtin CM (2021) Feed endoxylanase type and dose affect arabinoxylan hydrolysis and fermentation in ageing broilers. Animal Nutrition 7, 787–800.
Feed endoxylanase type and dose affect arabinoxylan hydrolysis and fermentation in ageing broilers.Crossref | GoogleScholarGoogle Scholar |

Bedford MR (2018) The evolution and application of enzymes in the animal feed industry: the role of data interpretation. British Poultry Science 59, 486–493.
The evolution and application of enzymes in the animal feed industry: the role of data interpretation.Crossref | GoogleScholarGoogle Scholar |

Bedford MR, Apajalahti J (2018) Exposure of a broiler to a xylanase for 35d increases the capacity of cecal microbiome to ferment soluble xylan. Poultry Science 97, 98–99.

Bedford MR, Apajalahti JH (2022) The role of feed enzymes in maintaining poultry intestinal health. Journal of the Science of Food and Agriculture 102, 1759–1770.
The role of feed enzymes in maintaining poultry intestinal health.Crossref | GoogleScholarGoogle Scholar |

Belenguer A, Duncan SH, Calder AG, Holtrop G, Louis P, Lobley GE, Flint HJ (2006) Two routes of metabolic cross-feeding between Bifidobacterium adolescentis and butyrate-producing anaerobes from the human gut. Applied and Environmental Microbiology 72, 3593–3599.
Two routes of metabolic cross-feeding between Bifidobacterium adolescentis and butyrate-producing anaerobes from the human gut.Crossref | GoogleScholarGoogle Scholar |

Biggs P, Parsons CM, Fahey GC (2007) The effects of several oligosaccharides on growth performance, nutrient digestibilities, and cecal microbial populations in young chicks. Poultry Science 86, 2327–2336.
The effects of several oligosaccharides on growth performance, nutrient digestibilities, and cecal microbial populations in young chicks.Crossref | GoogleScholarGoogle Scholar |

Bindari YR, Gerber PF (2022) Centennial Review: Factors affecting the chicken gastrointestinal microbial composition and their association with gut health and productive performance. Poultry Science 101,
Centennial Review: Factors affecting the chicken gastrointestinal microbial composition and their association with gut health and productive performance.Crossref | GoogleScholarGoogle Scholar |

Björnhag G, Sperber I (1977) Transport of various food components through the digestive tract of turkeys, geese and guinea fowl. Swedish Journal of Agricultural Research 7, 57–66.

Borda-Molina D, Mátis G, Mackei M, Neogrády Z, Huber K, Seifert J, Camarinha-Silva A (2021) Caeca microbial variation in broiler chickens as a result of dietary combinations using two cereal types, supplementation of crude protein and sodium butyrate. Frontiers in Microbiology 11,
Caeca microbial variation in broiler chickens as a result of dietary combinations using two cereal types, supplementation of crude protein and sodium butyrate.Crossref | GoogleScholarGoogle Scholar |

Broekaert WF, Courtin CM, Verbeke K, Van de Wiele T, Verstraete W, Delcour JA (2011) Prebiotic and other health-related effects of cereal-derived arabinoxylans, arabinoxylan-oligosaccharides, and xylooligosaccharides. Critical Reviews in Food Science and Nutrition 51, 178–194.
Prebiotic and other health-related effects of cereal-derived arabinoxylans, arabinoxylan-oligosaccharides, and xylooligosaccharides.Crossref | GoogleScholarGoogle Scholar |

Burton RA, Fincher GB (2014) Evolution and development of cell walls in cereal grains. Frontiers in Plant Science 5,
Evolution and development of cell walls in cereal grains.Crossref | GoogleScholarGoogle Scholar |

Canani RB, Costanzo MD, Leone L, Pedata M, Meli R, Calignano A (2011) Potential beneficial effects of butyrate in intestinal and extraintestinal diseases. World Journal of Gastroenterology 17, 1519–1528.
Potential beneficial effects of butyrate in intestinal and extraintestinal diseases.Crossref | GoogleScholarGoogle Scholar |

Cao BH, Karasawa Y, Guo YM (2005) Effects of green tea polyphenols and fructo-oligosaccharides in semi-purified diets on broilers’ performance and caecal microflora and their metabolites. Asian-Australasian Journal of Animal Sciences 18, 85–89.
Effects of green tea polyphenols and fructo-oligosaccharides in semi-purified diets on broilers’ performance and caecal microflora and their metabolites.Crossref | GoogleScholarGoogle Scholar |

Carvalho AFA, Neto PdO, da Silva DF, Pastore GM (2013) Xylo-oligosaccharides from lignocellulosic materials: chemical structure, health benefits and production by chemical and enzymatic hydrolysis. Food Research International 51, 75–85.
Xylo-oligosaccharides from lignocellulosic materials: chemical structure, health benefits and production by chemical and enzymatic hydrolysis.Crossref | GoogleScholarGoogle Scholar |

Casteleyn C, Doom M, Lambrechts E, Van den Broeck W, Simoens P, Cornillie P (2010) Locations of gut-associated lymphoid tissue in the 3-month-old chicken: a review. Avian Pathology 39, 143–150.
Locations of gut-associated lymphoid tissue in the 3-month-old chicken: a review.Crossref | GoogleScholarGoogle Scholar |

Chang L, Ding Y, Wang Y, Song Z, Li F, He X, Zhang H (2022) Effects of different oligosaccharides on growth performance and intestinal function in broilers. Frontiers in Veterinary Science 9,
Effects of different oligosaccharides on growth performance and intestinal function in broilers.Crossref | GoogleScholarGoogle Scholar |

Choct M, Hughes RJ, Wang J, Bedford MR, Morgan AJ, Annison G (1996) Increased small intestinal fermentation is partly responsible for the anti-nutritive activity of non-starch polysaccharides in chickens. British Poultry Science 37, 609–621.
Increased small intestinal fermentation is partly responsible for the anti-nutritive activity of non-starch polysaccharides in chickens.Crossref | GoogleScholarGoogle Scholar |

Clavijo V, Flórez MJV (2018) The gastrointestinal microbiome and its association with the control of pathogens in broiler chicken production: a review. Poultry Science 97, 1006–1021.
The gastrointestinal microbiome and its association with the control of pathogens in broiler chicken production: a review.Crossref | GoogleScholarGoogle Scholar |

Courtin CM, Broekaert WF, Swennen K, Lescroart O, Onagbesan O, Buyse J, Decuypere E, Van de Wiele T, Marzorati M, Verstraete W, Huyghebaert G, Delcour JA (2008) Dietary inclusion of wheat bran arabinoxylooligosaccharides induces beneficial nutritional effects in chickens. Cereal Chemistry 85, 607–613.
Dietary inclusion of wheat bran arabinoxylooligosaccharides induces beneficial nutritional effects in chickens.Crossref | GoogleScholarGoogle Scholar |

Craig AD, Khattak F, Hastie P, Bedford MR, Olukosi OA (2020a) Xylanase and xylo- oligosaccharide prebiotic improve the growth performance and concentration of potentially prebiotic oligosaccharides in the ileum of broiler chickens. British Poultry Science 61, 70–78.
Xylanase and xylo- oligosaccharide prebiotic improve the growth performance and concentration of potentially prebiotic oligosaccharides in the ileum of broiler chickens.Crossref | GoogleScholarGoogle Scholar |

Craig AD, Khattak F, Hastie P, Bedford MR, Olukosi OA (2020b) The similarity of the effect of carbohydrase or prebiotic supplementation in broilers aged 21 days, fed mixed cereal diets and challenged with coccidiosis infection. PLoS ONE 15,
The similarity of the effect of carbohydrase or prebiotic supplementation in broilers aged 21 days, fed mixed cereal diets and challenged with coccidiosis infection.Crossref | GoogleScholarGoogle Scholar |

Crisol-Martínez E, Stanley D, Geier MS, Hughes RJ, Moore RJ (2017) Sorghum and wheat differentially affect caecal microbiota and associated performance characteristics of meat chickens. PeerJ 5,
Sorghum and wheat differentially affect caecal microbiota and associated performance characteristics of meat chickens.Crossref | GoogleScholarGoogle Scholar |

Dale T, Hannay I, Bedford MR, Tucker GA, Brameld JM, Parr T (2020) The effects of exogenous xylanase supplementation on the in vivo generation of xylooligosaccharides and monosaccharides in broilers fed a wheat-based diet. British Poultry Science 61, 471–481.
The effects of exogenous xylanase supplementation on the in vivo generation of xylooligosaccharides and monosaccharides in broilers fed a wheat-based diet.Crossref | GoogleScholarGoogle Scholar |

De Maesschalck C, Eeckhaut V, Maertens L, De Lange L, Marchal L, Nezer C, De Baere S, Croubels S, Daube G, Dewulf J, Haesebrouck F, Ducatelle R, Taminau B, Van Immerseel F (2015) Effects of xylo-oligosaccharides on broiler chicken performance and microbiota. Applied and Environmental Microbiology 81, 5880–5888.
Effects of xylo-oligosaccharides on broiler chicken performance and microbiota.Crossref | GoogleScholarGoogle Scholar |

Ding XM, Li DD, Bai SP, Wang JP, Zeng QF, Su ZW, Xuan Y, Zhang KY (2018) Effect of dietary xylooligosaccharides on intestinal characteristics, gut microbiota, cecal short-chain fatty acids, and plasma immune parameters of laying hens. Poultry Science 97, 874–881.
Effect of dietary xylooligosaccharides on intestinal characteristics, gut microbiota, cecal short-chain fatty acids, and plasma immune parameters of laying hens.Crossref | GoogleScholarGoogle Scholar |

Donalson LM, Kim WK, Chalova VI, Herrera P, McReynolds JL, Gotcheva VG, Vidanović D, Woodward CL, Kubena LF, Nisbet DJ, Ricke SC (2008) In vitro fermentation response of laying hen cecal bacteria to combinations of fructooligosaccharide prebiotics with alfalfa or a layer ration. Poultry Science 87, 1263–1275.
In vitro fermentation response of laying hen cecal bacteria to combinations of fructooligosaccharide prebiotics with alfalfa or a layer ration.Crossref | GoogleScholarGoogle Scholar |

Duke GE, Eccleston E, Kirkwood S, Louis CF, Bedbury HP (1984) Cellulose digestion by domestic turkeys fed low or high fiber diets. The Journal of Nutrition 114, 95–102.
Cellulose digestion by domestic turkeys fed low or high fiber diets.Crossref | GoogleScholarGoogle Scholar |

Elling-Staats ML, Gilbert MS, Smidt H, Kwakkel RP (2022) Caecal protein fermentation in broilers: a review. World’s Poultry Science Journal 78, 103–123.
Caecal protein fermentation in broilers: a review.Crossref | GoogleScholarGoogle Scholar |

Engberg RM, Hedemann MS, Steenfeldt S, Jensen BB (2004) Influence of whole wheat and xylanase on broiler performance and microbial composition and activity in the digestive tract. Poultry Science 83, 925–938.
Influence of whole wheat and xylanase on broiler performance and microbial composition and activity in the digestive tract.Crossref | GoogleScholarGoogle Scholar |

Fathima S, Shanmugasundaram R, Adams D, Selvaraj RK (2022) Gastrointestinal microbiota and their manipulation for improved growth and performance in chickens. Foods 11,
Gastrointestinal microbiota and their manipulation for improved growth and performance in chickens.Crossref | GoogleScholarGoogle Scholar |

Ferrer R, Planas JM, Durfort M, Moretó M (1991) Morphological study of the caecal epithelium of the chicken (Gallus Gallus Domesticus L.). British Poultry Science 32, 679–691.
Morphological study of the caecal epithelium of the chicken (Gallus Gallus Domesticus L.).Crossref | GoogleScholarGoogle Scholar |

Feye KM, Baxter MFA, Tellez-Isaias G, Kogut MH, Ricke SC (2020) Influential factors on the composition of the conventionally raised broiler gastrointestinal microbiomes. Poultry Science 99, 653–659.
Influential factors on the composition of the conventionally raised broiler gastrointestinal microbiomes.Crossref | GoogleScholarGoogle Scholar |

Glendinning L, Watson KA, Watson M (2019) Development of the duodenal, ileal, jejunal and caecal microbiota in chickens. Animal Microbiome 1,
Development of the duodenal, ileal, jejunal and caecal microbiota in chickens.Crossref | GoogleScholarGoogle Scholar |

Glendinning L, Stewart RD, Pallen MJ, Watson KA, Watson M (2020) Assembly of hundreds of novel bacterial genomes from the chicken caecum. Genome Biology 21,
Assembly of hundreds of novel bacterial genomes from the chicken caecum.Crossref | GoogleScholarGoogle Scholar |

Gong J, Forster RJ, Yu H, Chambers JR, Sabour PM, Wheatcroft R, Chen S (2002) Diversity and phylogenetic analysis of bacteria in the mucosa of chicken ceca and comparison with bacteria in the cecal lumen. FEMS Microbiology Letters 208, 1–7.
Diversity and phylogenetic analysis of bacteria in the mucosa of chicken ceca and comparison with bacteria in the cecal lumen.Crossref | GoogleScholarGoogle Scholar |

Gong J, Yu H, Liu T, Gill JJ, Chambers JR, Wheatcroft R, Sabour PM (2008) Effects of zinc bacitracin, bird age and access to range on bacterial microbiota in the ileum and caeca of broiler chickens. Journal of Applied Microbiology 104, 1372–1382.
Effects of zinc bacitracin, bird age and access to range on bacterial microbiota in the ileum and caeca of broiler chickens.Crossref | GoogleScholarGoogle Scholar |

Gonzalez-Ortiz G, Gomes GA, dos Santos TT, Bedford MR (2019) New strategies influencing gut functionality and animal performance. In ‘The value of fibre – engaging the second brain for animal nutrition’. (Eds G González-Ortiz, MR Bedford, KE Bach Knudsen, CM Courtin, HL Classen) pp. 233–254. (Wageningen Academic Press: Netherlands)

González-Ortiz G, Olukosi OA, Jurgens G, Apajalahti J, Bedford MR (2020) Short-chain fatty acids and ceca microbiota profiles in broilers and turkeys in response to diets supplemented with phytase at varying concentrations, with or without xylanase. Poultry Science 99, 2068–2077.
Short-chain fatty acids and ceca microbiota profiles in broilers and turkeys in response to diets supplemented with phytase at varying concentrations, with or without xylanase.Crossref | GoogleScholarGoogle Scholar |

Guilloteau P, Martin L, Eeckhaut V, Ducatelle R, Zabielski R, Van Immerseel F (2010) From the gut to the peripheral tissues: the multiple effects of butyrate. Nutrition Research Reviews 23, 366–384.
From the gut to the peripheral tissues: the multiple effects of butyrate.Crossref | GoogleScholarGoogle Scholar |

Hunt A, Al-Nakkash L, Lee AH, Smith HF (2019) Phylogeny and herbivory are related to avian cecal size. Scientific Reports 9,
Phylogeny and herbivory are related to avian cecal size.Crossref | GoogleScholarGoogle Scholar |

Ijaz UZ, Sivaloganathan L, McKenna A, Richmond A, Kelly C, Linton M, Stratakos AC, Lavery U, Elmi A, Wren BW, Dorrell N, Corcionivoschi N, Gundogdu O (2018) Comprehensive longitudinal microbiome analysis of the chicken cecum reveals a shift from competitive to environmental drivers and a window of opportunity for campylobacter. Frontiers in Microbiology 9,
Comprehensive longitudinal microbiome analysis of the chicken cecum reveals a shift from competitive to environmental drivers and a window of opportunity for campylobacter.Crossref | GoogleScholarGoogle Scholar |

Jahan AA, González Ortiz G, Moss AF, Bhuiyan MM, Morgan NK (2022) Role of supplemental oligosaccharides in poultry diets. World’s Poultry Science Journal 78, 615–639.
Role of supplemental oligosaccharides in poultry diets.Crossref | GoogleScholarGoogle Scholar |

Janssen PWM, Lentle RG, Hulls C, Ravindran V, Amerah AM (2009) Spatiotemporal mapping of the motility of the isolated chicken caecum. Journal of Comparative Physiology B 179, 593–604.
Spatiotemporal mapping of the motility of the isolated chicken caecum.Crossref | GoogleScholarGoogle Scholar |

Józefiak D, Rutkowski A, Frątczak M, Boros D (2004) The effect of dietary fibre fractions from different cereals and microbial enzyme supplementation on performance, ileal viscosity and short-chain fatty acid concentrations in the caeca of broiler chickens. Journal of Animal and Feed Sciences 13, 487–496.
The effect of dietary fibre fractions from different cereals and microbial enzyme supplementation on performance, ileal viscosity and short-chain fatty acid concentrations in the caeca of broiler chickens.Crossref | GoogleScholarGoogle Scholar |

Józefiak D, Rutkowski A, Jensen BB, Engberg RM (2006) The effect of β-glucanase supplementation of barley- and oat-based diets on growth performance and fermentation in broiler chicken gastrointestinal tract. British Poultry Science 47, 57–64.
The effect of β-glucanase supplementation of barley- and oat-based diets on growth performance and fermentation in broiler chicken gastrointestinal tract.Crossref | GoogleScholarGoogle Scholar |

Józefiak D, Rutkowski A, Kaczmarek S, Jensen BB, Engberg RM, Højberg O (2010) Effect of β-glucanase and xylanase supplementation of barley- and rye-based diets on caecal microbiota of broiler chickens. British Poultry Science 51, 546–557.
Effect of β-glucanase and xylanase supplementation of barley- and rye-based diets on caecal microbiota of broiler chickens.Crossref | GoogleScholarGoogle Scholar |

Keerqin C, Morgan NK, Wu SB, Swick RA, Choct M (2017) Dietary inclusion of arabinoxylo-oligosaccharides in response to broilers challenged with subclinical necrotic enteritis. British Poultry Science 58, 418–424.
Dietary inclusion of arabinoxylo-oligosaccharides in response to broilers challenged with subclinical necrotic enteritis.Crossref | GoogleScholarGoogle Scholar |

Kers JG, Oliveira JE, Fischer EAJ, Tersteeg-Zijderveld MHG, Konstanti P, Stegeman JA(Arjan), Smidt H, Velkers FC (2020) Associations between phenotypic characteristics and clinical parameters of broilers and intestinal microbial development throughout a production cycle: a field study. MicrobiologyOpen 9,
Associations between phenotypic characteristics and clinical parameters of broilers and intestinal microbial development throughout a production cycle: a field study.Crossref | GoogleScholarGoogle Scholar |

Kim E, Moss AF, Morgan NK, Gharib-Naseri K, Ader P, Choct M (2022) Non-starch polysaccharide-degrading enzymes may improve performance when included in wheat- but not maize-based diets fed to broiler chickens under subclinical necrotic enteritis challenge. Animal Nutrition 10, 54–67.
Non-starch polysaccharide-degrading enzymes may improve performance when included in wheat- but not maize-based diets fed to broiler chickens under subclinical necrotic enteritis challenge.Crossref | GoogleScholarGoogle Scholar |

Langhout DJ, Schutte JB (1996) Nutritional implications of pectins in chicks in relation to esterification and origin of pectins. Poultry Science 75, 1236–1242.
Nutritional implications of pectins in chicks in relation to esterification and origin of pectins.Crossref | GoogleScholarGoogle Scholar |

Li J, Cheng Y, Chen Y, Qu H, Zhao Y, Wen C, Zhou Y (2019) Dietary chitooligosaccharide inclusion as an alternative to antibiotics improves intestinal morphology, barrier function, antioxidant capacity, and immunity of broilers at early age. Animals 9,
Dietary chitooligosaccharide inclusion as an alternative to antibiotics improves intestinal morphology, barrier function, antioxidant capacity, and immunity of broilers at early age.Crossref | GoogleScholarGoogle Scholar |

Liao X, Shao Y, Sun G, Yang Y, Zhang L, Guo Y, Luo X, Lu L (2020) The relationship among gut microbiota, short-chain fatty acids, and intestinal morphology of growing and healthy broilers. Poultry Science 99, 5883–5895.
The relationship among gut microbiota, short-chain fatty acids, and intestinal morphology of growing and healthy broilers.Crossref | GoogleScholarGoogle Scholar |

Lin Y, Teng P-Y, Olukosi OA (2022) The effects of xylo-oligosaccharides on regulating growth performance, nutrient utilization, gene expression of tight junctions, nutrient transporters, and cecal short chain fatty acids profile in Eimeria-challenged broiler chickens. Poultry Science 101,
The effects of xylo-oligosaccharides on regulating growth performance, nutrient utilization, gene expression of tight junctions, nutrient transporters, and cecal short chain fatty acids profile in Eimeria-challenged broiler chickens.Crossref | GoogleScholarGoogle Scholar |

Liu HY, Li X, Zhu X, Dong WG, Yang GQ (2021a) Soybean oligosaccharides attenuate odour compounds in excreta by modulating the caecal microbiota in broilers. Animal 15,
Soybean oligosaccharides attenuate odour compounds in excreta by modulating the caecal microbiota in broilers.Crossref | GoogleScholarGoogle Scholar |

Liu L, Li Q, Yang Y, Guo A (2021b) Biological function of short-chain fatty acids and its regulation on intestinal health of poultry. Frontiers in Veterinary Science 8,
Biological function of short-chain fatty acids and its regulation on intestinal health of poultry.Crossref | GoogleScholarGoogle Scholar |

Longstaff MA, Knox A, McNab JM (1988) Digestibility of pentose sugars and uronic acids and their effect on chick weight gain and caecal size. British Poultry Science 29, 379–393.
Digestibility of pentose sugars and uronic acids and their effect on chick weight gain and caecal size.Crossref | GoogleScholarGoogle Scholar |

Lu J, Idris U, Harmon B, Hofacre C, Maurer JJ, Lee MD (2003) Diversity and succession of the intestinal bacterial community of the maturing broiler chicken. Applied and Environmental Microbiology 69, 6816–6824.
Diversity and succession of the intestinal bacterial community of the maturing broiler chicken.Crossref | GoogleScholarGoogle Scholar |

Mahmood T, Guo Y (2020) Dietary fiber and chicken microbiome interaction: where will it lead to? Animal Nutrition 6, 1–8.
Dietary fiber and chicken microbiome interaction: where will it lead to?Crossref | GoogleScholarGoogle Scholar |

Majeed MF, Al-Asadi FS, Al-Nassir AN, Rahi EH (2009) The morphological and histological study of the caecum in broiler chicken. Basrah Journal of Veterinary Research 8, 19–25.
The morphological and histological study of the caecum in broiler chicken.Crossref | GoogleScholarGoogle Scholar |

Mateos GG, Jiménez-Moreno E, Serrano MP, Lázaro RP (2012) Poultry response to high levels of dietary fiber sources varying in physical and chemical characteristics. Journal of Applied Poultry Research 21, 156–174.
Poultry response to high levels of dietary fiber sources varying in physical and chemical characteristics.Crossref | GoogleScholarGoogle Scholar |

McNab JM (1973) The avian caeca: a review. World’s Poultry Science Journal 29, 251–263.
The avian caeca: a review.Crossref | GoogleScholarGoogle Scholar |

Metzler-Zebeli BU, Magowan E, Hollmann M, Ball MEE, Molnár A, Witter K, Ertl R, Hawken RJ, Lawlor PG, O’Connell NE, Aschenbach J, Zebeli Q (2018) Differences in intestinal size, structure, and function contributing to feed efficiency in broiler chickens reared at geographically distant locations. Poultry Science 97, 578–591.
Differences in intestinal size, structure, and function contributing to feed efficiency in broiler chickens reared at geographically distant locations.Crossref | GoogleScholarGoogle Scholar |

Mirande C, Kadlecikova E, Matulova M, Capek P, Bernalier-Donadille A, Forano E, Béra-Maillet C (2010) Dietary fibre degradation and fermentation by two xylanolytic bacteria Bacteroides xylanisolvens XB1AT and Roseburia intestinalis XB6B4 from the human intestine. Journal of Applied Microbiology 109, 451–460.
Dietary fibre degradation and fermentation by two xylanolytic bacteria Bacteroides xylanisolvens XB1AT and Roseburia intestinalis XB6B4 from the human intestine.Crossref | GoogleScholarGoogle Scholar |

Modrackova N, Vlkova E, Tejnecky V, Schwab C, Neuzil-Bunesova V (2020) Bifidobacterium β-glucosidase activity and fermentation of dietary plant glucosides is species and strain specific. Microorganisms 8,
Bifidobacterium β-glucosidase activity and fermentation of dietary plant glucosides is species and strain specific.Crossref | GoogleScholarGoogle Scholar |

Mookiah S, Sieo CC, Ramasamy K, Abdullah N, Ho YW (2014) Effects of dietary prebiotics, probiotic and synbiotics on performance, caecal bacterial populations and caecal fermentation concentrations of broiler chickens. Journal of the Science of Food and Agriculture 94, 341–348.
Effects of dietary prebiotics, probiotic and synbiotics on performance, caecal bacterial populations and caecal fermentation concentrations of broiler chickens.Crossref | GoogleScholarGoogle Scholar |

Morgan NK, Keerqin C, Wallace A, Wu S-B, Choct M (2019) Effect of arabinoxylo-oligosaccharides and arabinoxylans on net energy and nutrient utilization in broilers. Animal Nutrition 5, 56–62.
Effect of arabinoxylo-oligosaccharides and arabinoxylans on net energy and nutrient utilization in broilers.Crossref | GoogleScholarGoogle Scholar |

Morgan NK, Wallace A, Bedford MR, Hawking KL, Rodrigues I, Hilliar M, Choct M (2020) In vitro versus in situ evaluation of xylan hydrolysis into xylo-oligosaccharides in broiler chicken gastrointestinal tract. Carbohydrate Polymers 230,
In vitro versus in situ evaluation of xylan hydrolysis into xylo-oligosaccharides in broiler chicken gastrointestinal tract.Crossref | GoogleScholarGoogle Scholar |

Morgan NK, Gomes GA, Kim JC (2021) Comparing the efficacy of stimbiotic and a combination of xylanase and beta-glucanase, in broilers fed wheat-barley based diets with high or low AME. Poultry Science 100,
Comparing the efficacy of stimbiotic and a combination of xylanase and beta-glucanase, in broilers fed wheat-barley based diets with high or low AME.Crossref | GoogleScholarGoogle Scholar |

Morgan NK, Wallace A, Bedford MR (2022a) Improving sorghum digestion in broilers by targeting fermentation of xylan. Animal Nutrition 10, 198–206.
Improving sorghum digestion in broilers by targeting fermentation of xylan.Crossref | GoogleScholarGoogle Scholar |

Morgan NK, Wallace A, Bedford MR, González-Ortiz G (2022b) Impact of fermentable fiber, xylo-oligosaccharides and xylanase on laying hen productive performance and nutrient utilization. Poultry Science 101,
Impact of fermentable fiber, xylo-oligosaccharides and xylanase on laying hen productive performance and nutrient utilization.Crossref | GoogleScholarGoogle Scholar |

Moura P, Barata R, Carvalheiro F, Gírio F, Loureiro-Dias MC, Esteves MP (2007) In vitro fermentation of xylo-oligosaccharides from corn cobs autohydrolysis by Bifidobacterium and Lactobacillus strains. LWT - Food Science and Technology 40, 963–972.
In vitro fermentation of xylo-oligosaccharides from corn cobs autohydrolysis by Bifidobacterium and Lactobacillus strains.Crossref | GoogleScholarGoogle Scholar |

Munyaka PM, Nandha NK, Kiarie E, Nyachoti CM, Khafipour E (2016) Impact of combined β-glucanase and xylanase enzymes on growth performance, nutrients utilization and gut microbiota in broiler chickens fed corn or wheat-based diets. Poultry Science 95, 528–540.
Impact of combined β-glucanase and xylanase enzymes on growth performance, nutrients utilization and gut microbiota in broiler chickens fed corn or wheat-based diets.Crossref | GoogleScholarGoogle Scholar |

Mussatto SI, Mancilha IM (2007) Non-digestible oligosaccharides: a review. Carbohydrate Polymers 68, 587–597.
Non-digestible oligosaccharides: a review.Crossref | GoogleScholarGoogle Scholar |

Nguyen HT, Bedford MR, Morgan NK (2021) Importance of considering non-starch polysaccharide content of poultry diets. World’s Poultry Science Journal 77, 619–637.
Importance of considering non-starch polysaccharide content of poultry diets.Crossref | GoogleScholarGoogle Scholar |

Oakley BB, Buhr RJ, Ritz CW, Kiepper BH, Berrang ME, Seal BS, Cox NA (2014) Successional changes in the chicken cecal microbiome during 42 days of growth are independent of organic acid feed additives. BMC Veterinary Research 10,
Successional changes in the chicken cecal microbiome during 42 days of growth are independent of organic acid feed additives.Crossref | GoogleScholarGoogle Scholar |

Okazaki M, Fujikawa S, Matsumoto N (1990) Effect of xylooligosaccharide on the growth of bifidobacteria. Bifidobacteria and Microflora 9, 77–86.
Effect of xylooligosaccharide on the growth of bifidobacteria.Crossref | GoogleScholarGoogle Scholar |

Olukosi OA, Bedford MR (2019) Comparative effects of wheat varieties and xylanase supplementation on growth performance, nutrient utilization, net energy, and whole-body energy and nutrient partitioning in broilers at different ages. Poultry Science 98, 2179–2188.
Comparative effects of wheat varieties and xylanase supplementation on growth performance, nutrient utilization, net energy, and whole-body energy and nutrient partitioning in broilers at different ages.Crossref | GoogleScholarGoogle Scholar |

Paraskeuas V, Mountzouris KC (2019) Broiler gut microbiota and expressions of gut barrier genes affected by cereal type and phytogenic inclusion. Animal Nutrition 5, 22–31.
Broiler gut microbiota and expressions of gut barrier genes affected by cereal type and phytogenic inclusion.Crossref | GoogleScholarGoogle Scholar |

Patel DS, Pendrill R, Mallajosyula SS, Widmalm G, MacKerell AD (2014) Conformational properties of α- or β-(1→6)-linked oligosaccharides: Hamiltonian replica exchange MD simulations and NMR experiment. The Journal of Physical Chemistry B 118, 2851–2871.
Conformational properties of α- or β-(1→6)-linked oligosaccharides: Hamiltonian replica exchange MD simulations and NMR experiment.Crossref | GoogleScholarGoogle Scholar |

Pedroso AA, Batal AB, Lee MD (2016) Effect of in ovo administration of an adult-derived microbiota on establishment of the intestinal microbiome in chickens. American Journal of Veterinary Research 77, 514–526.
Effect of in ovo administration of an adult-derived microbiota on establishment of the intestinal microbiome in chickens.Crossref | GoogleScholarGoogle Scholar |

Pottenger S, Watts A, Wedley A, Jopson S, Darby AC, Wigley P (2023) Timing and delivery route effects of cecal microbiome transplants on Salmonella typhimurium infections in chickens: potential for in-hatchery delivery of microbial interventions. Animal Microbiome 5,
Timing and delivery route effects of cecal microbiome transplants on Salmonella typhimurium infections in chickens: potential for in-hatchery delivery of microbial interventions.Crossref | GoogleScholarGoogle Scholar |

Pourabedin M, Zhao X (2015) Prebiotics and gut microbiota in chickens. FEMS Microbiology Letters 362,
Prebiotics and gut microbiota in chickens.Crossref | GoogleScholarGoogle Scholar |

Pourabedin M, Guan L, Zhao X (2015) Xylo-oligosaccharides and virginiamycin differentially modulate gut microbial composition in chickens. Microbiome 3,
Xylo-oligosaccharides and virginiamycin differentially modulate gut microbial composition in chickens.Crossref | GoogleScholarGoogle Scholar |

Pourabedin M, Chen Q, Yang M, Zhao X (2017) Mannan- and xylooligosaccharides modulate caecal microbiota and expression of inflammatory-related cytokines and reduce caecal salmonella enteritidis colonisation in young chickens. FEMS Microbiology Ecology 93,
Mannan- and xylooligosaccharides modulate caecal microbiota and expression of inflammatory-related cytokines and reduce caecal salmonella enteritidis colonisation in young chickens.Crossref | GoogleScholarGoogle Scholar |

Radeff T (1928) Über die Rohfaserverdauung beim Huhn und die hierbei dem Blinddarm zukommende Bedeutung. Biocehmische Zeitschrift 193, 192–196.

Ramírez GA, Keshri J, Vahrson I, Garber AI, Berrang ME, Cox NA, González-Cerón F, Aggrey SE, Oakley BB (2022) Cecal microbial hydrogen cycling potential is linked to feed efficiency phenotypes in chickens. Frontiers in Veterinary Science 9,
Cecal microbial hydrogen cycling potential is linked to feed efficiency phenotypes in chickens.Crossref | GoogleScholarGoogle Scholar |

Rehman H, Böhm J, Zentek J (2008) Effects of differentially fermentable carbohydrates on the microbial fermentation profile of the gastrointestinal tract of broilers. Journal of Animal Physiology and Animal Nutrition 92, 471–480.
Effects of differentially fermentable carbohydrates on the microbial fermentation profile of the gastrointestinal tract of broilers.Crossref | GoogleScholarGoogle Scholar |

Ribeiro T, Cardoso V, Ferreira LMA, Lordelo MMS, Coelho E, Moreira ASP, Domingues MRM, Coimbra MA, Bedford MR, Fontes CMGA (2018) Xylo-oligosaccharides display a prebiotic activity when used to supplement wheat or corn-based diets for broilers. Poultry Science 97, 4330–4341.
Xylo-oligosaccharides display a prebiotic activity when used to supplement wheat or corn-based diets for broilers.Crossref | GoogleScholarGoogle Scholar |

Richards P, Fothergill J, Bernardeau M, Wigley P (2019) Development of the caecal microbiota in three broiler breeds. Frontiers in Veterinary Science 6,
Development of the caecal microbiota in three broiler breeds.Crossref | GoogleScholarGoogle Scholar |

Ricke SC, Lee SI, Kim SA, Park SH, Shi Z (2020) Prebiotics and the poultry gastrointestinal tract microbiome. Poultry Science 99, 670–677.
Prebiotics and the poultry gastrointestinal tract microbiome.Crossref | GoogleScholarGoogle Scholar |

Rodríguez ML, Rebolé A, Velasco S, Ortiz LT, Treviño J, Alzueta C (2012) Wheat- and barley-based diets with or without additives influence broiler chicken performance, nutrient digestibility and intestinal microflora. Journal of the Science of Food and Agriculture 92, 184–190.
Wheat- and barley-based diets with or without additives influence broiler chicken performance, nutrient digestibility and intestinal microflora.Crossref | GoogleScholarGoogle Scholar |

Rycroft CE, Jones MR, Gibson GR, Rastall RA (2001) A comparative in vitro evaluation of the fermentation properties of prebiotic oligosaccharides. Journal of Applied Microbiology 91, 878–887.
A comparative in vitro evaluation of the fermentation properties of prebiotic oligosaccharides.Crossref | GoogleScholarGoogle Scholar |

Sacranie A, Iji PA, Mikkelsen LL, Choct M (2007) Occurrence of reverse peristalsis in broiler chickens. In ‘Proceedings of the 19th Australian poultry science symposium, 12–14 February, Sydney, New South Wales, Australia’. pp. 161–164. (Poultry Research Foundation)

Sacranie A, Svihus B, Denstadli V, Moen B, Iji PA, Choct M (2012) The effect of insoluble fiber and intermittent feeding on gizzard development, gut motility, and performance of broiler chickens. Poultry Science 91, 693–700.
The effect of insoluble fiber and intermittent feeding on gizzard development, gut motility, and performance of broiler chickens.Crossref | GoogleScholarGoogle Scholar |

Samanta AK, Jayapal N, Kolte AP, Senani S, Sridhar M, Dhali A, Suresh KP, Jayaram C, Prasad CS (2015) Process for enzymatic production of xylooligosaccharides from the xylan of corn cobs. Journal of Food Processing and Preservation 39, 729–736.
Process for enzymatic production of xylooligosaccharides from the xylan of corn cobs.Crossref | GoogleScholarGoogle Scholar |

Samanta AK, Kotte AP, Elangovan AV, Dhali A, Senani S, Sridhar M, Jayapal N (2017) Effects of corn husks derived xylooligosaccharides on performance of broiler chicken. Indian Journal of Animal Science 87, 640–643.

Sergeant MJ, Constantinidou C, Cogan TA, Bedford MR, Penn CW, Pallen MJ (2014) Extensive microbial and functional diversity within the chicken cecal microbiome. PLoS ONE 9,
Extensive microbial and functional diversity within the chicken cecal microbiome.Crossref | GoogleScholarGoogle Scholar |

Shini S, Bryden WL (2022) Probiotics and gut health: linking gut homeostasis and poultry productivity. Animal Production Science 62, 1090–1112.
Probiotics and gut health: linking gut homeostasis and poultry productivity.Crossref | GoogleScholarGoogle Scholar |

Singh AK, Mishra B, Bedford MR, Jha R (2021) Effects of supplemental xylanase and xylooligosaccharides on production performance and gut health variables of broiler chickens. Journal of Animal Science and Biotechnology 12,
Effects of supplemental xylanase and xylooligosaccharides on production performance and gut health variables of broiler chickens.Crossref | GoogleScholarGoogle Scholar |

Singh AK, Tiwari UP, Mishra B, Jha R (2022) Effects of in ovo delivered xylo- and mannan- oligosaccharides on growth performance, intestinal immunity, cecal short-chain fatty acids, and cecal microbiota of broilers. Journal of Animal Science and Biotechnology 13,
Effects of in ovo delivered xylo- and mannan- oligosaccharides on growth performance, intestinal immunity, cecal short-chain fatty acids, and cecal microbiota of broilers.Crossref | GoogleScholarGoogle Scholar |

Stanley D, Geier MS, Hughes RJ, Denman SE, Moore RJ (2013) Highly variable microbiota development in the chicken gastrointestinal tract. PLoS ONE 8,
Highly variable microbiota development in the chicken gastrointestinal tract.Crossref | GoogleScholarGoogle Scholar |

Suo H-Q, Lu L, Xu G-H, Xiao L, Chen X-G, Xia R-R, Zhang L-Y, Luo X-G (2015) Effectiveness of dietary xylo-oligosaccharides for broilers fed a conventional corn-soybean meal diet. Journal of Integrative Agriculture 14, 2050–2057.
Effectiveness of dietary xylo-oligosaccharides for broilers fed a conventional corn-soybean meal diet.Crossref | GoogleScholarGoogle Scholar |

Svihus B, Choct M, Classen HL (2013) Function and nutritional roles of the avian caeca: a review. World’s Poultry Science Journal 69, 249–264.
Function and nutritional roles of the avian caeca: a review.Crossref | GoogleScholarGoogle Scholar |

Torok VA, Hughes RJ, Ophel-Keller K, Ali M, MacAlpine R (2009) Influence of different litter materials on cecal microbiota colonization in broiler chickens. Poultry Science 88, 2474–2481.
Influence of different litter materials on cecal microbiota colonization in broiler chickens.Crossref | GoogleScholarGoogle Scholar |

van der Wielen PWJJ, Biesterveld S, Notermans S, Hofstra H, Urlings BAP, van Knapen F (2000) Role of volatile fatty acids in development of the cecal microflora in broiler chickens during growth. Applied and Environmental Microbiology 66, 2536–2540.
Role of volatile fatty acids in development of the cecal microflora in broiler chickens during growth.Crossref | GoogleScholarGoogle Scholar |

Wang Y, Wang Y, Lin X, Gou Z, Fan Q, Jiang S (2021) Effects of Clostridium butyricum, sodium butyrate, and butyric acid glycerides on the reproductive performance, egg quality, intestinal health, and offspring performance of yellow-feathered breeder hens. Frontiers in Microbiology 12,
Effects of Clostridium butyricum, sodium butyrate, and butyric acid glycerides on the reproductive performance, egg quality, intestinal health, and offspring performance of yellow-feathered breeder hens.Crossref | GoogleScholarGoogle Scholar |

Warriss PD, Wilkins LJ, Brown SN, Phillips AJ, Allen V (2004) Defaecation and weight of the gastrointestinal tract contents after feed and water withdrawal in broilers. British Poultry Science 45, 61–66.
Defaecation and weight of the gastrointestinal tract contents after feed and water withdrawal in broilers.Crossref | GoogleScholarGoogle Scholar |

Wickramasuriya SS, Park I, Lee K, Lee Y, Kim WH, Nam H, Lillehoj HS (2022) Role of physiology, immunity, microbiota, and infectious diseases in the gut health of poultry. Vaccines 10,
Role of physiology, immunity, microbiota, and infectious diseases in the gut health of poultry.Crossref | GoogleScholarGoogle Scholar |

Xiao X, Wang Y, He J, Li Y (2020) Effects of Xylooligosaccharide (XOS) and Probiotics (PRO) on production performance, egg quality and intestinal short-chain fatty acids of laying hens in late laying period. Animal Husbandry and Feed Science 12, 21–25.

Xu ZR, Hu CH, Xia MS, Zhan XA, Wang MQ (2003) Effects of dietary fructooligosaccharide on digestive enzyme activities, intestinal microflora and morphology of male broilers. Poultry Science 82, 1030–1036.
Effects of dietary fructooligosaccharide on digestive enzyme activities, intestinal microflora and morphology of male broilers.Crossref | GoogleScholarGoogle Scholar |

Yang C, Qiu M, Zhang Z, Song X, Yang L, Xiong X, Hu C, Pen H, Chen J, Xia B, Du H, Li Q, Jiang X, Yu C (2022) Galacto-oligosaccharides and xylo-oligosaccharides affect meat flavor by altering the cecal microbiome, metabolome, and transcriptome of chickens. Poultry Science 101,
Galacto-oligosaccharides and xylo-oligosaccharides affect meat flavor by altering the cecal microbiome, metabolome, and transcriptome of chickens.Crossref | GoogleScholarGoogle Scholar |

Yousaf MS, Ahmad I, Ashraf K, Rashid MA, Hafeez A, Ahmad A, Zaneb H, Naseer R, Numan M, Zentek J, Rehman H (2017) Comparative effects of different dietary concentrations of β- galacto-oligosaccharides on serum biochemical metabolites, selected caecel microbiota and immune response in broilers. The Journal of Animal and Plant Science 27, 98–105.

Yuan L, Li W, Huo Q, Du C, Wang Z, Yi B, Wang M (2018) Effects of xylo-oligosaccharide and flavomycin on the immune function of broiler chickens. PeerJ 6,
Effects of xylo-oligosaccharide and flavomycin on the immune function of broiler chickens.Crossref | GoogleScholarGoogle Scholar |

Zhang WF, Li DF, Lu WQ, Yi GF (2003) Effects of isomalto-oligosaccharides on broiler performance and intestinal microflora. Poultry Science 82, 657–663.
Effects of isomalto-oligosaccharides on broiler performance and intestinal microflora.Crossref | GoogleScholarGoogle Scholar |

Zhou J, Wu S, Qi G, Fu Y, Wang W, Zhang H, Wang J (2021) Dietary supplemental xylooligosaccharide modulates nutrient digestibility, intestinal morphology, and gut microbiota in laying hens. Animal Nutrition 7, 152–162.
Dietary supplemental xylooligosaccharide modulates nutrient digestibility, intestinal morphology, and gut microbiota in laying hens.Crossref | GoogleScholarGoogle Scholar |

Zhu X, Liu J, Liu H, Yang G (2020) Soybean oligosaccharide, stachyose, and raffinose in broilers diets: effects on odor compound concentration and microbiota in cecal digesta. Poultry Science 99, 3532–3539.
Soybean oligosaccharide, stachyose, and raffinose in broilers diets: effects on odor compound concentration and microbiota in cecal digesta.Crossref | GoogleScholarGoogle Scholar |

Zhu X, Xu M, Liu H, Yang G (2022) In vitro fermentation profiles of different soybean oligosaccharides and their effects on skatole production and cecal microbiota of broilers. Animal Bioscience 35, 1195–1204.
In vitro fermentation profiles of different soybean oligosaccharides and their effects on skatole production and cecal microbiota of broilers.Crossref | GoogleScholarGoogle Scholar |

Zyla K, Gogol D, Koreleski J, Swiatkiewicz S, Ledoux DR (1999) Simultaneous application of phytase and xylanase to broiler feeds based on wheat: in vitro measurements of phosphorus and pentose release from wheats and wheat-based feeds. Journal of the Science of Food and Agriculture 79, 1832–1840.