Effects of different grains on bacterial diversity and enzyme activity associated with digestion of starch in the foal stomach.
Abstract: Compared with the stomach of ruminant cattle, the stomach of horse is small and mainly for chemical digestion, but the microorganisms in the stomach play an important role in maintaining the homeostasis of the internal environment. Due to the complexity of the microbes in the stomach, little is known about the diversity and structure of bacteria in the equine stomach. Grains are the main energy source for plant-eating livestock and energy is derived through enzymatic hydrolysis of grains into glucose or their microbial fermentation into Volatile fatty acids (VFA). However, the mechanism through which these ingested grains are chemically digested as well as the effect of these grains on the stomach remains elusive. This study explored the effects of feeding different grains (corn, oats, and barley) on bacterial diversity, structure, and composition in the foal's stomach content. Furthermore, the effects of different grains on the vitality of starch digestion-related stomach enzymes were investigated. Results: No significant differences were observed (P > 0.05) in the bacterial rarefaction curves of Operational Taxonomic Units (OTUs) and diversity of the stomach microbiota in all foals. This study also revealed the statistical differences for Firmicutes, Cyanobacteria, Actinobacteria, Fibrobacteres, Lactobacillaceae, Streptococcaceae, Unidentified_Clostridiales, Prevotellaceae, Lactobacillus, Streptococcus, Unidentified_Cyanobacteria, Unidentified_Clostridiales, Lactococcus, Sphingomonas, Lactobacillus_hayakitensis, Lactobacillus_equigenerosi, and Clostridium_perfringens. The linear discriminant analysis effect size analysis revealed 9 bacteria at each classification level. The functional analysis of species information by using FAPROTAX software was able to predict 35 functions, and the top 5 functions were chemoheterotrophy, fermentation, animal_parasites_or_symbionts, nitrate_reduction, and aerobic_chemoheterotrophy. The study also revealed statistical differences for pH, glucose concentration, β-amylase, maltase, and amylase. Conclusions: The different grains had no significant effect on the microbial diversity of the stomach content of the foal. However, the relative bacterial abundances differed significantly in response to different diets. Particularly, oats fed to the foals significantly increased the relative abundance of Firmicutes, Lactobacillaceae, Lactobacillus, and Lactobacillus_hayakitensis. The grain had no significant effect on the pH of the stomach content, glucose concentration, and enzyme viability in the foal.
© 2022. The Author(s).
Publication Date: 2022-11-17 PubMed ID: 36397114PubMed Central: PMC9670411DOI: 10.1186/s12917-022-03510-2Google Scholar: Lookup
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Summary
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This research paper investigates the impact of different types of grains (corn, oats, and barley) on the diversity and structure of bacteria found in the stomach of foals, as well as the vitality of specific enzymes related to digestion. The study concluded that while the grains did not significantly affect overall microbial diversity or enzyme vitality, they did cause distinct changes in the relative abundance of certain types of bacteria.
Research Approach and Findings
- The authors embarked on this study due to a lack of knowledge regarding the diversity and structure of bacteria in the equine stomach. They wanted to see how this might be influenced by feeding foals different grains, which serve as the main energy source for plant-eating livestock.
- The grains are broken down into glucose via enzymatic hydrolysis or by microbial fermentation into volatile fatty acids (VFA) for energy.
- Observations revealed that the species and amounts of bacteria varied in different feed types, though the overall diversity didn’t significantly change. More specifically, the grains caused significant differences in the relative abundances of certain bacteria, including Firmicutes, Cyanobacteria, Actinobacteria, among others.
- Interestingly, the study found that feeding foals oats specifically resulted in a significant increase in the relative abundance of Firmicutes, Lactobacillaceae, Lactobacillus, and Lactobacillus_hayakitensis.
Implications of the Study
- The fact that individual grains, despite not affecting overall microbial diversity, can influence the abundance of specific bacteria could have practical implications for feeding practices in equines.
- Each type of grain could potentially be used to encourage growth of specific bacterial populations in the foal gut for improved digestion and health.
- However, further study is required to understand how changes in bacterial abundance translate into effects on the horse’s overall health and well-being.
Conclusion
- The study concludes that the type of grain fed to foals does not significantly impact the overall microbial diversity or the viability of starch-digesting enzymes in the stomach. However, it does affect the relative abundance of certain types of bacteria.
Cite This Article
APA
Li XB, Huang XX, Li Q, Li XY, Li JH, Li C, He LJ, Jing HX, Yang KL.
(2022).
Effects of different grains on bacterial diversity and enzyme activity associated with digestion of starch in the foal stomach.
BMC Vet Res, 18(1), 407.
https://doi.org/10.1186/s12917-022-03510-2 Publication
Researcher Affiliations
- College of Animal Science, Xinjiang Agricultural University, Xinjiang Key Laboratory of Herbivore Nutrition for Meat & Milk Production, Urumqi, Xinjiang, 830052, China.
- College of Animal Science, Xinjiang Agricultural University, Xinjiang Key Laboratory of Herbivore Nutrition for Meat & Milk Production, Urumqi, Xinjiang, 830052, China.
- College of Animal Science, Xinjiang Agricultural University, Xinjiang Key Laboratory of Herbivore Nutrition for Meat & Milk Production, Urumqi, Xinjiang, 830052, China.
- College of Animal Science, Xinjiang Agricultural University, Xinjiang Key Laboratory of Herbivore Nutrition for Meat & Milk Production, Urumqi, Xinjiang, 830052, China.
- College of Animal Science, Xinjiang Agricultural University, Xinjiang Key Laboratory of Herbivore Nutrition for Meat & Milk Production, Urumqi, Xinjiang, 830052, China.
- College of Animal Science, Xinjiang Agricultural University, Xinjiang Key Laboratory of Herbivore Nutrition for Meat & Milk Production, Urumqi, Xinjiang, 830052, China.
- College of Animal Science, Xinjiang Agricultural University, Xinjiang Key Laboratory of Herbivore Nutrition for Meat & Milk Production, Urumqi, Xinjiang, 830052, China.
- College of Animal Science, Xinjiang Agricultural University, Xinjiang Key Laboratory of Herbivore Nutrition for Meat & Milk Production, Urumqi, Xinjiang, 830052, China.
- College of Animal Science, Xinjiang Agricultural University, Xinjiang Key Laboratory of Herbivore Nutrition for Meat & Milk Production, Urumqi, Xinjiang, 830052, China. 490735574@qq.com.
MeSH Terms
- Animals
- Bacteria / classification
- Digestion
- Edible Grain
- Glucose
- Horses
- Starch / metabolism
- Stomach / metabolism
- Stomach / microbiology
- Animal Feed
Conflict of Interest Statement
The authors declare that they have no competing interests.
References
This article includes 88 references
- Costa MC, Silva G, Ramos RV, Staempfli HR, Arroyo LG, Kim P, Weese JS. Characterization and comparison of the bacterial microbiota in different gastrointestinal tract compartments in horses.. Vet J 2015 Jul;205(1):74-80.
- Borda-Molina D, Vital M, Sommerfeld V, Rodehutscord M, Camarinha-Silva A. Insights into Broilers' Gut Microbiota Fed with Phosphorus, Calcium, and Phytase Supplemented Diets.. Front Microbiol 2016;7:2033.
- Varloud M, Fonty G, Roussel A, Guyonvarch A, Julliand V. Postprandial kinetics of some biotic and abiotic characteristics of the gastric ecosystem of horses fed a pelleted concentrate meal.. J Anim Sci 2007 Oct;85(10):2508-16.
- Coenen M, Mösseler A, Vervuert I. Fermentative gases in breath indicate that inulin and starch start to be degraded by microbial fermentation in the stomach and small intestine of the horse in contrast to pectin and cellulose.. J Nutr 2006 Jul;136(7 Suppl):2108S-2110S.
- Al Jassim RAM. Supplementary feeding of hoeses with processed sorghum grains and osts. Anim Feed Sci Technol 2006;125(1–2):33–44.
- Kong BW, Kim JI, Kim MJ, Kim JC. Porcine pancreatic alpha-amylase hydrolysis of native starch granules as a function of granule surface area.. Biotechnol Prog 2003 Jul-Aug;19(4):1162-6.
- Svihus B, Uhlen AK, Harstad OM. Effect of starch granule structure,associated components and processing on nutritive value of cereal starch: A review. Anim Feed Sci Technol 2005;122(3–4):303–320.
- de Fombelle A, Veiga L, Drogoul C, Julliand V. Effect of diet composition and feeding pattern on the prececal digestibility of starches from diverse botanical origins measured with the mobile nylon bag technique in horses.. J Anim Sci 2004 Dec;82(12):3625-34.
- Harlow BE. Impact of Starch Source on Equine Hindgut Microbial Ecology. [PhD Thesis] Lexington: Kentucky University; 2015.
- Yao QF, Zhao YP, Mang L, Wu NEF. Study Progress on diversity of germplasm resources of Chinese local horses. Animal Husbandry and Feed Science 2009;30(10):126–130.
- Harlow BE, Lawrence LM, Hayes SH, Crum A, Flythe MD. Effect of Dietary Starch Source and Concentration on Equine Fecal Microbiota.. PLoS One 2016;11(4):e0154037.
- Magoč T, Salzberg SL. FLASH: fast length adjustment of short reads to improve genome assemblies.. Bioinformatics 2011 Nov 1;27(21):2957-63.
- Behrendt L, Larkum AW, Trampe E, Norman A, Sørensen SJ, Kühl M. Microbial diversity of biofilm communities in microniches associated with the didemnid ascidian Lissoclinum patella.. ISME J 2012 Jun;6(6):1222-37.
- Caporaso JG, Kuczynski J, Stombaugh J, Bittinger K, Bushman FD, Costello EK, Fierer N, Peña AG, Goodrich JK, Gordon JI, Huttley GA, Kelley ST, Knights D, Koenig JE, Ley RE, Lozupone CA, McDonald D, Muegge BD, Pirrung M, Reeder J, Sevinsky JR, Turnbaugh PJ, Walters WA, Widmann J, Yatsunenko T, Zaneveld J, Knight R. QIIME allows analysis of high-throughput community sequencing data.. Nat Methods 2010 May;7(5):335-6.
- Wang Q, Garrity GM, Tiedje JM, Cole JR. Naive Bayesian classifier for rapid assignment of rRNA sequences into the new bacterial taxonomy.. Appl Environ Microbiol 2007 Aug;73(16):5261-7.
- Bokulich NA, Subramanian S, Faith JJ, Gevers D, Gordon JI, Knight R, Mills DA, Caporaso JG. Quality-filtering vastly improves diversity estimates from Illumina amplicon sequencing.. Nat Methods 2013 Jan;10(1):57-9.
- Edgar RC, Haas BJ, Clemente JC, Quince C, Knight R. UCHIME improves sensitivity and speed of chimera detection.. Bioinformatics 2011 Aug 15;27(16):2194-200.
- Haas BJ, Gevers D, Earl AM, Feldgarden M, Ward DV, Giannoukos G, Ciulla D, Tabbaa D, Highlander SK, Sodergren E, Methé B, DeSantis TZ, Petrosino JF, Knight R, Birren BW. Chimeric 16S rRNA sequence formation and detection in Sanger and 454-pyrosequenced PCR amplicons.. Genome Res 2011 Mar;21(3):494-504.
- Edgar RC. UPARSE: highly accurate OTU sequences from microbial amplicon reads.. Nat Methods 2013 Oct;10(10):996-8.
- Quast C, Pruesse E, Yilmaz P, Gerken J, Schweer T, Yarza P, Peplies J, Glöckner FO. The SILVA ribosomal RNA gene database project: improved data processing and web-based tools.. Nucleic Acids Res 2013 Jan;41(Database issue):D590-6.
- Edgar RC. MUSCLE: multiple sequence alignment with high accuracy and high throughput.. Nucleic Acids Res 2004;32(5):1792-7.
- SAS statistical analysis system. Users guide, statistics, version 9.2. Cary: SAS Institute; 2008.
- Li B, Zhang X, Guo F, Wu W, Zhang T. Characterization of tetracycline resistant bacterial community in saline activated sludge using batch stress incubation with high-throughput sequencing analysis.. Water Res 2013 Sep 1;47(13):4207-16.
- Aßhauer KP, Wemheuer B, Daniel R, Meinicke P. Tax4Fun: predicting functional profiles from metagenomic 16S rRNA data.. Bioinformatics 2015 Sep 1;31(17):2882-4.
- Segata N, Izard J, Waldron L, Gevers D, Miropolsky L, Garrett WS, Huttenhower C. Metagenomic biomarker discovery and explanation.. Genome Biol 2011 Jun 24;12(6):R60.
- Al Jassim RA, Andrews FM. The bacterial community of the horse gastrointestinal tract and its relation to fermentative acidosis, laminitis, colic, and stomach ulcers.. Vet Clin North Am Equine Pract 2009 Aug;25(2):199-215.
- Moore BE, Dehority BA. Effects of diet and hindgut defaunation on diet digestibility and microbial concentrations in the cecum and colon of the horse.. J Anim Sci 1993 Dec;71(12):3350-8.
- Costa MC, Weese JS. The equine intestinal microbiome.. Anim Health Res Rev 2012 Jun;13(1):121-8.
- Palmer C, Bik EM, DiGiulio DB, Relman DA, Brown PO. Development of the human infant intestinal microbiota.. PLoS Biol 2007 Jul;5(7):e177.
- Hansen CH, Nielsen DS, Kverka M, Zakostelska Z, Klimesova K, Hudcovic T, Tlaskalova-Hogenova H, Hansen AK. Patterns of early gut colonization shape future immune responses of the host.. PLoS One 2012;7(3):e34043.
- Yamamoto M, Yamaguchi R, Munakata K, Takashima K, Nishiyama M, Hioki K, Ohnishi Y, Nagasaki M, Imoto S, Miyano S, Ishige A, Watanabe K. A microarray analysis of gnotobiotic mice indicating that microbial exposure during the neonatal period plays an essential role in immune system development.. BMC Genomics 2012 Jul 23;13:335.
- Zhou Y, Burnham CA, Hink T, Chen L, Shaikh N, Wollam A, Sodergren E, Weinstock GM, Tarr PI, Dubberke ER. Phenotypic and genotypic analysis of Clostridium difficile isolates: a single-center study.. J Clin Microbiol 2014 Dec;52(12):4260-6.
- Dougal K, de la Fuente G, Harris PA, Girdwood SE, Pinloche E, Newbold CJ. Identification of a core bacterial community within the large intestine of the horse.. PLoS One 2013;8(10):e77660.
- O' Donnell MM, Harris HM, Jeffery IB, Claesson MJ, Younge B, O' Toole PW, Ross RP. The core faecal bacterial microbiome of Irish Thoroughbred racehorses.. Lett Appl Microbiol 2013 Dec;57(6):492-501.
- Stewart CJ, Marrs EC, Magorrian S, Nelson A, Lanyon C, Perry JD, Embleton ND, Cummings SP, Berrington JE. The preterm gut microbiota: changes associated with necrotizing enterocolitis and infection.. Acta Paediatr 2012 Nov;101(11):1121-7.
- Conlan S, Kong HH, Segre JA. Species-level analysis of DNA sequence data from the NIH Human Microbiome Project.. PLoS One 2012;7(10):e47075.
- Proudman CJ, Hunter JO, Darby AC, Escalona EE, Batty C, Turner C. Characterisation of the faecal metabolome and microbiome of Thoroughbred racehorses.. Equine Vet J 2015 Sep;47(5):580-6.
- Yatsunenko T, Rey FE, Manary MJ, Trehan I, Dominguez-Bello MG, Contreras M, Magris M, Hidalgo G, Baldassano RN, Anokhin AP, Heath AC, Warner B, Reeder J, Kuczynski J, Caporaso JG, Lozupone CA, Lauber C, Clemente JC, Knights D, Knight R, Gordon JI. Human gut microbiome viewed across age and geography.. Nature 2012 May 9;486(7402):222-7.
- Sakaitani Y, Yuki N, Nakajima F, Nakanishi S, Tanaka H, Tanaka R. Colonization of intestinal microflora in newborn foals. J Intest Microbiol 1999;13(1):9–14.
- Fonty G, Chaucheyras-Durand F. Les écosystèmes digestifs. Tec Et Doc & Em Inter & Lavoisier 2017.
- Combes S, Michelland RJ, Monteils V, Cauquil L, Soulié V, Tran NU, Gidenne T, Fortun-Lamothe L. Postnatal development of the rabbit caecal microbiota composition and activity.. FEMS Microbiol Ecol 2011 Sep;77(3):680-9.
- Meyer H, Radicke S, Kienzle E, Wilke S, Kleffken D, Illenseer M. Investigations on preileal digestion of starch from grain, potato and manioc in horses.. Zentralbl Veterinarmed A 1995 Aug;42(6):371-81.
- Rosenfeld I, Austbø D. Digestion of cereals in the equine gastrointestinal tract measured by the mobile bag technique on caecally cannulated horses. Anim Feed Sci Technol 2009;150(3–4):249–258.
- Radicke S, Kienzle E, Meyer H. Preileal apparent digestibility of oats and corn starch and consequences for cecal metabolism. In: In Proceedings of the 12th Equine Nutrition and Physiology Symposium. Calgary: Equine Nutrition and Physiology Society edition, in English; 1991, p. 43–8.
- Harlow BE, Donley TM, Lawrence LM, Flythe MD. Effect of starch source (corn, oats or wheat) and concentration on fermentation by equine faecal microbiota in vitro.. J Appl Microbiol 2015 Nov;119(5):1234-44.
- Schoster A, Staempfli HR, Guardabassi LG, Jalali M, Weese JS. Comparison of the fecal bacterial microbiota of healthy and diarrheic foals at two and four weeks of life.. BMC Vet Res 2017 May 30;13(1):144.
- Fernandes KA, Kittelmann S, Rogers CW, Gee EK, Bolwell CF, Bermingham EN, Thomas DG. Faecal microbiota of forage-fed horses in New Zealand and the population dynamics of microbial communities following dietary change.. PLoS One 2014;9(11):e112846.
- Roswall J, Olsson LM, Kovatcheva-Datchary P, Nilsson S, Tremaroli V, Simon MC, Kiilerich P, Akrami R, Krämer M, Uhlén M, Gummesson A, Kristiansen K, Dahlgren J, Bäckhed F. Developmental trajectory of the healthy human gut microbiota during the first 5 years of life.. Cell Host Microbe 2021 May 12;29(5):765-776.e3.
- Rodriguez C, Taminiau B, Brévers B, Avesani V, Van Broeck J, Leroux A, Gallot M, Bruwier A, Amory H, Delmée M, Daube G. Faecal microbiota characterisation of horses using 16 rdna barcoded pyrosequencing, and carriage rate of clostridium difficile at hospital admission.. BMC Microbiol 2015 Sep 16;15:181.
- Li XB, Huang XX, Zang CJ, Ma C, Chen KX, Zhao GD, Li Q, Li XY, Zhang WJ, Yang KL. Effects of steam-flaked grains on foals' growth and faecal microbiota.. BMC Vet Res 2021 Sep 4;17(1):293.
- Thompson KN, Jackson SG, Baker JP. Apparent digestion coefficients and associative effects of varying hay: grain ratios fed to horses. Nut Rep Intern 1984;30(1):189–197.
- Julliand V, De Fombelle A, Drogoul C, Jacotot E. Feeding and microbial disorders in horses: part 3—effects of three hay: grain ratios on microbial profile and activities. Journal of Equine Veterinary Science 2001;21(11):543–546.
- Drogoul C, De Fombelle A, Julliand V. Feeding and microbial disorders in horses: 2: effect of three hay: grain ratios on digesta passage rate and digestibility in ponies. Journal of Equine Veterinary Science 2001;21(10):487–491.
- Medina B, Girard ID, Jacotot E, Julliand V. Effect of a preparation of Saccharomyces cerevisiae on microbial profiles and fermentation patterns in the large intestine of horses fed a high fiber or a high starch diet.. J Anim Sci 2002 Oct;80(10):2600-9.
- Pei L, Yang H, Qin S, Yan Z, Zhang H, Lan Y, Li A, Iqbal M, Shen Y. Isolation and Evaluation of Probiotic Potential of Lactic Acid Strains From Healthy Equines for Potential Use in Salmonella Infection.. J Equine Vet Sci 2021 Jan;96:103312.
- Varloud M, De Fombelle A, Goachet AG, Drogoul C, Julliand V. Partial and total apparent digestibility of dietary carbohydrates in horses as affected by the diet. Anim Sci 2004;79(1):61–72.
- Costa MC, Arroyo LG, Allen-Vercoe E, Stämpfli HR, Kim PT, Sturgeon A, Weese JS. Comparison of the fecal microbiota of healthy horses and horses with colitis by high throughput sequencing of the V3-V5 region of the 16S rRNA gene.. PLoS One 2012;7(7):e41484.
- Milinovich GJ, Trott DJ, Burrell PC, van Eps AW, Thoefner MB, Blackall LL, Al Jassim RA, Morton JM, Pollitt CC. Changes in equine hindgut bacterial populations during oligofructose-induced laminitis.. Environ Microbiol 2006 May;8(5):885-98.
- Elliott J, Bailey SR. Gastrointestinal derived factors are potential triggers for the development of acute equine laminitis.. J Nutr 2006 Jul;136(7 Suppl):2103S-2107S.
- Muhonen S, Wartena FC, Wesker A, Julliand V. Effect of three different forage-based diets on microbial flora, pH and viscosity of the equine hindgut. In: Ellis AD, Longland AC, Coenen M, Miraglia N, editors. The impact of nutrition on the health and welfare of horses. Wageningen: Wageningen Academic Publishers; 2010. pp. 196–198.
- Van den Berg M, Hoskin SO, Rogers CW, Grinberg A. Fecal pH and microbial populations in thoroughbred horses during transition from pasture to concentrate feeding. Journal of Equine Veterinary Science 2013;33(4):215–222.
- Morita H, Shimazu M, Shiono H, Toh H, Nakajima F, Akita H, Takagi M, Takami H, Murakami M, Masaoka T, Tanabe S, Hattori M. Lactobacillus equicursoris sp. nov., isolated from the faeces of a thoroughbred racehorse.. Int J Syst Evol Microbiol 2010 Jan;60(Pt 1):109-112.
- Al Jassim RA, Scott PT, Trebbin AL, Trott D, Pollitt CC. The genetic diversity of lactic acid producing bacteria in the equine gastrointestinal tract.. FEMS Microbiol Lett 2005 Jul 1;248(1):75-81.
- Endo A, Okada S, Morita H. Molecular profiling of Lactobacillus, Streptococcus, and Bifidobacterium species in feces of active racehorses.. J Gen Appl Microbiol 2007 Jun;53(3):191-200.
- Morotomi M, Yuki N, Kado Y, Kushiro A, Shimazaki T, Watanabe K, Yuyama T. Lactobacillus equi sp. nov., a predominant intestinal Lactobacillus species of the horse isolated from faeces of healthy horses.. Int J Syst Evol Microbiol 2002 Jan;52(Pt 1):211-214.
- Morita H, Shiratori C, Murakami M, Takami H, Kato Y, Endo A, Nakajima F, Takagi M, Akita H, Okada S, Masaoka T. Lactobacillus hayakitensis sp. nov., isolated from intestines of healthy thoroughbreds.. Int J Syst Evol Microbiol 2007 Dec;57(Pt 12):2836-2839.
- Endo A, Roos S, Satoh E, Morita H, Okada S. Lactobacillus equigenerosi sp. nov., a coccoid species isolated from faeces of thoroughbred racehorses.. Int J Syst Evol Microbiol 2008 Apr;58(Pt 4):914-8.
- Li Y, Liu C, Liu Q, Liu W. Comparative Genomic Analysis Reveals Intestinal Habitat Adaptation of Ligilactobacillus equi Rich in Prophage and Degrading Cellulase.. Molecules 2022 Mar 14;27(6).
- Dec M, Stępień-Pyśniak D, Puchalski A, Hauschild T, Pietras-Ożga D, Ignaciuk S, Urban-Chmiel R. Biodiversity of Ligilactobacillus salivarius Strains from Poultry and Domestic Pigeons.. Animals (Basel) 2021 Mar 31;11(4).
- Yao M, Lu Y, Zhang T, Xie J, Han S, Zhang S, Fei Y, Ling Z, Wu J, Hu Y, Ji S, Chen H, Berglund B, Li L. Improved functionality of Ligilactobacillus salivarius Li01 in alleviating colonic inflammation by layer-by-layer microencapsulation.. NPJ Biofilms Microbiomes 2021 Jul 9;7(1):58.
- Jia D, Wang Y, Wang J, Liu J, Li H, Liu A, Wang J, Guan G, Luo J, Yin H, Li Y. Lactobacillus animalis pZL8a: a potential probiotic isolated from pig feces for further research.. 3 Biotech 2021 Mar;11(3):132.
- Morita H, Nakano A, Shimazu M, Toh H, Nakajima F, Nagayama M, Hisamatsu S, Kato Y, Takagi M, Takami H, Akita H, Matsumoto M, Masaoka T, Murakami M. Lactobacillus hayakitensis, L. equigenerosi and L. equi, predominant lactobacilli in the intestinal flora of healthy thoroughbreds.. Anim Sci J 2009 Jun;80(3):339-46.
- Candela M, Maccaferri S, Turroni S, Carnevali P, Brigidi P. Functional intestinal microbiome, new frontiers in prebiotic design.. Int J Food Microbiol 2010 Jun 15;140(2-3):93-101.
- Kedia G, Vázquez JA, Charalampopoulos D, Pandiella SS. In vitro fermentation of oat bran obtained by debranning with a mixed culture of human fecal bacteria.. Curr Microbiol 2009 Apr;58(4):338-42.
- Shen RL, Dang XY, Dong JL, Hu XZ. Effects of oat β-glucan and barley β-glucan on fecal characteristics, intestinal microflora, and intestinal bacterial metabolites in rats.. J Agric Food Chem 2012 Nov 14;60(45):11301-8.
- Carman RJ, Sayeed S, Li J, Genheimer CW, Hiltonsmith MF, Wilkins TD, McClane BA. Clostridium perfringens toxin genotypes in the feces of healthy North Americans.. Anaerobe 2008 Apr;14(2):102-8.
- Gao J, Zhang CM, Liu W, Zhao YL, Zhao BH. Progress on ε toxin of Clostridium perfringens type D. Progress in Veterinary Medicine 2013;34(10):101–105.
- Chen XY, Guan FS, Zhang CS, Zhou LG. Recent progress on the major toxins of Clostridium perfringens. Chinese Journal of Veterinary Drug 2005;06:29–33.
- Czeczulin JR, Collie RE, McClane BA. Regulated expression of Clostridium perfringens enterotoxin in naturally cpe-negative type A, B, and C isolates of C. perfringens.. Infect Immun 1996 Aug;64(8):3301-9.
- Annett CB, Viste JR, Chirino-Trejo M, Classen HL, Middleton DM, Simko E. Necrotic enteritis: effect of barley, wheat and corn diets on proliferation of Clostridium perfringens type A.. Avian Pathol 2002 Dec;31(6):598-601.
- China Feed Database. Institute of Animal Science of CAAS, BeiJing,China. 2022. http://www.chinafeeddata.org.cn Accessed 25 Aug 2022.
- Pimentel M, Lin HC, Enayati P, van den Burg B, Lee HR, Chen JH, Park S, Kong Y, Conklin J. Methane, a gas produced by enteric bacteria, slows intestinal transit and augments small intestinal contractile activity.. Am J Physiol Gastrointest Liver Physiol 2006 Jun;290(6):G1089-95.
- Langille MG, Zaneveld J, Caporaso JG, McDonald D, Knights D, Reyes JA, Clemente JC, Burkepile DE, Vega Thurber RL, Knight R, Beiko RG, Huttenhower C. Predictive functional profiling of microbial communities using 16S rRNA marker gene sequences.. Nat Biotechnol 2013 Sep;31(9):814-21.
- Martinsen TC, Bergh K, Waldum HL. Gastric juice: a barrier against infectious diseases.. Basic Clin Pharmacol Toxicol 2005 Feb;96(2):94-102.
- Wang W, Chen L, Zhou R, Wang X, Song L, Huang S, Wang G, Xia B. Increased proportions of Bifidobacterium and the Lactobacillus group and loss of butyrate-producing bacteria in inflammatory bowel disease.. J Clin Microbiol 2014 Feb;52(2):398-406.
- Wang FM, Fan MS, Zheng KK. Nutritive value of oat β-glucan and the factors affecting its accumulation. Journal of Triticeae Crops 2005;02:116–118.
- Julliand V, De Fombelle A, Varloud M. Starch digestion in horses: the impact of feed processing. Livest Sci 2006;100(1):44–52.
- Kienzle E, Radicke S, Landes E, Kleffken D, Illenseer M, Meyer H. Activity of amylase in the gastrointestinal tract of the horse 1. J Anim Physiol Anim Nutr 1994;72(1–5):234–241.
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