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Journal of equine science2024; 34(4); 101-109; doi: 10.1294/jes.34.101

Effects of concentrate levels on intestinal fermentation and the microbial profile in Japanese draft horses.

Abstract: In racehorses, feeding a high-concentrate diet could cause abnormal fermentation in the hindgut. This feeding management regime is not suitable for the nutritional physiology of horses. However, studies on the hindgut environment have yet to be reported in Japanese draft horses, so feeding management needs to be investigated in these horses. Therefore, the objective of this study was to investigate the effects of a high-concentrate diet on hindgut fermentation in Japanese draft horses. Feces were collected from 20 male Japanese draft horses managed by two stables with different feeding designs (65% weight ratio of concentrate feed, HC; 50% weight ratio of concentrate, MC), and fecal metabolic characteristics and the microbiome were analyzed. Higher lactate concentrations and lower fecal pH levels were observed in the HC group (P=0.0011, P=0.0192, respectively). Fecal microbiome analysis revealed a decrease in microbial diversity (P=0.0360) and an increase in the relative abundance of Streptococcus lutetiensis/equinus/infantarius (P=0.0011) in the HC group. On the other hand, fibrolytic bacteria in the MC group had similarities with Clostridium sacchalolyticum and Ruminococcus albus. This study revealed that overfeeding of concentrates induced abnormal fermentation in the hindgut of Japanese draft horses. This suggests that the establishment of a feeding design based on not only the chemical compositions of feeds but also microbial dynamics is needed.
Publication Date: 2024-01-18 PubMed ID: 38274554PubMed Central: PMC10806360DOI: 10.1294/jes.34.101Google Scholar: Lookup
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  • Journal Article

Summary

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The research investigates the effects of high-concentrate diet on intestinal fermentation and microbial health in Japanese draft horses, showing that excessive concentrate intake can lead to abnormal fermentation and microbial imbalance.

Objective of the Research

  • The principal aim of the research was to explore the effects of a high-concentrate diet on the hindgut fermentation in Japanese draft horses.
  • Since there is limited research about the hindgut environment in Japanese draft horses, this study attempts to fill in the gap by revealing the overall impact of different feeding designs on the horse’s gut health.

Research Methods and Participants

  • The investigators collected fecal samples from 20 male Japanese draft horses managed by two stables.
  • The feeding designs of the stables were different: one provided a high concentrate diet that accounted for 65% weight ratio (HC group), and the other provided a moderate-concentrate diet equaling up to 50% weight ratio (MC group).
  • They analyzed the fecal metabolic characteristics and the microbiome of the samples to determine the impact of different levels of concentrate in the diet.

Findings

  • The study showed that the horses in the HC group experienced higher lactate concentrations and lower fecal pH levels. This is indicative of abnormal fermentation in the hindgut as a result of the high-concentrate diet.
  • Microbiome analysis revealed a decrease in microbial diversity and an increase in the relative abundance of Streptococcus lutetiensis/equinus/infantarius, bacteria linked to unbalanced gut flora.
  • On the other hand, fibrolytic bacteria in the MC group bore similarities with Clostridium sacchalolyticum and Ruminococcus albus species, beneficial to the gut health of the horses.

Implications

  • This research suggests that overfeeding of concentrate leads to abnormal fermentation in the hindgut of Japanese draft horses and impacts their overall health.
  • It hints towards the importance of establishing feeding designs based not only on the chemical compositions of feeds but also considering the dynamism of microbial health.

Cite This Article

APA
Yano R, Moriyama T, Fujimori M, Nishida T, Hanada M, Fukuma N. (2024). Effects of concentrate levels on intestinal fermentation and the microbial profile in Japanese draft horses. J Equine Sci, 34(4), 101-109. https://doi.org/10.1294/jes.34.101

Publication

ISSN: 1340-3516
NlmUniqueID: 9503751
Country: Japan
Language: English
Volume: 34
Issue: 4
Pages: 101-109

Researcher Affiliations

Yano, Rintaro
  • Graduate School of Animal Husbandry, Obihiro University of Agriculture and Veterinary Medicine, Hokkaido 080-8555, Japan.
Moriyama, Tomoe
  • Veterinary Medical Center, Obihiro University of Agriculture and Veterinary Medicine, Hokkaido 080-8555, Japan.
Fujimori, Miho
  • Graduate School of Animal Husbandry, Obihiro University of Agriculture and Veterinary Medicine, Hokkaido 080-8555, Japan.
Nishida, Takehiro
  • Department of Life and Food Sciences, Obihiro University of Agriculture and Veterinary Medicine, Hokkaido 080-8555, Japan.
Hanada, Masaaki
  • Department of Life and Food Sciences, Obihiro University of Agriculture and Veterinary Medicine, Hokkaido 080-8555, Japan.
Fukuma, Naoki
  • Department of Life and Food Sciences, Obihiro University of Agriculture and Veterinary Medicine, Hokkaido 080-8555, Japan.
  • Research Center for Global Agromedicine, Obihiro University of Agriculture and Veterinary Medicine, Hokkaido 080-8555, Japan.

References

This article includes 35 references
  1. Caporaso J.G., Kuczynski J., Stombaugh J., Bittinger K., Bushman F.D., Costello E.K., Fierer N., Peña A.G., Goodrich J.K., Gordon J.I., Huttley G.A., Kelley S.T., Knights D., Koenig J.E., Ley R.E., Lozupone C.A., McDonald D., Muegge B.D., Pirrung M., Reeder J., Sevinsky J.R., Turnbaugh P.J., Walters W.A., Widmann J., Yatsunenko T., Zaneveld J., Knight R.. QIIME allows analysis of high-throughput community sequencing data. Nat. Methods 7: 335–336.
    pmc: PMC3156573pubmed: 20383131
  2. Daly K., Proudman C.J., Duncan S.H., Flint H.J., Dyer J., Shirazi-Beechey S.P.. Alterations in microbiota and fermentation products in equine large intestine in response to dietary variation and intestinal disease. Br. J. Nutr. 107: 989–995.
    pubmed: 21816118
  3. Dassa B., Borovok I., Ruimy-Israeli V., Lamed R., Flint H.J., Duncan S.H., Henrissat B., Coutinho P., Morrison M., Mosoni P., Yeoman C.J., White B.A., Bayer E.A.. Rumen cellulosomics: divergent fiber-degrading strategies revealed by comparative genome-wide analysis of six ruminococcal strains. PLoS One 9: e99221.
    pmc: PMC4081043pubmed: 24992679
  4. Fernandes K.A., Kittelmann S., Rogers C.W., Gee E.K., Bolwell C.F., Bermingham E.N., Thomas D.G.. Faecal microbiota of forage-fed horses in New Zealand and the population dynamics of microbial communities following dietary change. PLoS One 9: e112846.
    pmc: PMC4226576pubmed: 25383707
  5. de Fombelle A., Julliand V., Drogoul C., Jacotot E.. Feeding and microbial disorders in horses: 1-effects of an abrupt incorporation of two levels of barley in a hay diet on microbial profile and activities. J. Equine Vet. Sci. 21: 439–445.
  6. Goodson J., Tyznik W.J., Cline J.H., Dehority B.A.. Effects of an abrupt diet change from hay to concentrate on microbial numbers and physical environment in the cecum of the pony. Appl. Environ. Microbiol. 54: 1946–1950.
    pmc: PMC202784pubmed: 3178206
  7. Henderson G., Cox F., Ganesh S., Jonker A., Young W., Janssen P.H., Global Rumen Census Collaborators. Rumen microbial community composition varies with diet and host, but a core microbiome is found across a wide geographical range. Sci. Rep. 5: 14567.
    pmc: PMC4598811pubmed: 26449758
  8. Hiraga A., Sugano S.. Studies on the exercise physiology of draft horses performed in Japan during the 1950s and 1960s. J. Equine Sci. 28: 1–12.
    pmc: PMC5383625pubmed: 28400701
  9. Julliand V., De Fombelle A., Varloud M.. Starch digestion in horses: the impact of feed processing. Livest. Sci. 100: 44–52.
  10. Kashiwamura F., Avgaandorj A., Furumura K.. Relationships among body size, conformation, and racing performance in Banei Draft Racehorses. J. Equine Sci. 12: 1–7.
  11. Koike S., Shingu Y., Inaba H., Kawai M., Kobayashi Y., Hata H., Tanaka K., Okubo M.. Fecal bacteria in Hokkaido native horses as characterized by microscopic enumeration and competitive polymerase chain reaction assays. J. Equine Sci. 11: 45–50.
  12. Liu J.H., Xu T.T., Liu Y.J., Zhu W.Y., Mao S.Y.. A high-grain diet causes massive disruption of ruminal epithelial tight junctions in goats. Am. J. Physiol. Regul. Integr. Comp. Physiol. 305: R232–R241.
    pubmed: 23739344
  13. Liu J., Xu T., Zhu W., Mao S.. High-grain feeding alters caecal bacterial microbiota composition and fermentation and results in caecal mucosal injury in goats. Br. J. Nutr. 112: 416–427.
    pubmed: 24846282
  14. Mackie R.I., Wilkins C.A.. Enumeration of anaerobic bacterial microflora of the equine gastrointestinal tract. Appl. Environ. Microbiol. 54: 2155–2160.
    pmc: PMC202828pubmed: 3190223
  15. Mao S.Y., Zhang R.Y., Wang D.S., Zhu W.Y.. Impact of subacute ruminal acidosis (SARA) adaptation on rumen microbiota in dairy cattle using pyrosequencing. Anaerobe 24: 12–19.
    pubmed: 23994204
  16. Mi L., Yang B., Hu X., Luo Y., Liu J., Yu Z., Wang J.. Comparative analysis of the microbiota between sheep rumen and rabbit cecum provides new insight into their differential methane production. Front. Microbiol. 9: 575.
    pmc: PMC5890152pubmed: 29662480
  17. Milinovich G.J., Trott D.J., Burrell P.C., van Eps A.W., Thoefner M.B., Blackall L.L., Al Jassim R.A.M., Morton J.M., Pollitt C.C.. Changes in equine hindgut bacterial populations during oligofructose-induced laminitis. Environ. Microbiol. 8: 885–898.
    pubmed: 16623745
  18. Milinovich G.J., Burrell P.C., Pollitt C.C., Klieve A.V., Blackall L.L., Ouwerkerk D., Woodland E., Trott D.J.. Microbial ecology of the equine hindgut during oligofructose-induced laminitis. ISME J. 2: 1089–1100.
    pubmed: 18580970
  19. Milinovich G.J., Trott D.J., Burrell P.C., Croser E.L., Al Jassim R.A.M., Morton J.M., van Eps A.W., Pollitt C.C.. Fluorescence in situ hybridization analysis of hindgut bacteria associated with the development of equine laminitis. Environ. Microbiol. 9: 2090–2100.
    pubmed: 17635552
  20. Miyazaki K., Hino T., Itabashi H.. Effects of extracellular pH on the intracellular pH and membrane potential of cellulolytic ruminal bacteria, Ruminococcus albus, Ruminococcus flavefaciens, and Fibrobacter succinogenes. J. Gen. Appl. Microbiol. 38: 567–573.
  21. Mungall B.A., Kyaw-Tanner M., Pollitt C.C.. In vitro evidence for a bacterial pathogenesis of equine laminitis. Vet. Microbiol. 79: 209–223.
    pubmed: 11240100
  22. Murray W.D.. Symbiotic Relationship of Bacteroides cellulosolvens and Clostridium saccharolyticum in Cellulose Fermentation. Appl. Environ. Microbiol. 51: 710–714.
    pmc: PMC238952pubmed: 16347034
  23. Murray W. D., Khan A.W., van den BERG L.. Clostridium saccharolyticum sp. nov., a saccharolytic species from sewage sludge. Int. J. Syst. Evol. Microbiol. 32: 132–135.
  24. Nagata R., Kamibayashi R., Bochimoto H., Fukuma N., Shimada K., Tachibe M., Takaishi Y., Han K.H., Fukushima M.. Chemical modification of cornstarch by hydroxypropylation enhances cecal fermentation‐mediated lipid metabolism in rats. Stärke 72: 1900050.
  25. Ouwerkerk J.P., Aalvink S., Belzer C., de Vos W.M.. Akkermansia glycaniphila sp. nov., an anaerobic mucin-degrading bacterium isolated from reticulated python faeces. Int. J. Syst. Evol. Microbiol. 66: 4614–4620.
    pubmed: 27499019
  26. Poyart C., Quesne G., Trieu-Cuot P.. Taxonomic dissection of the Streptococcus bovis group by analysis of manganese-dependent superoxide dismutase gene (sodA) sequences: reclassification of ‘Streptococcus infantarius subsp. coli’ as Streptococcus lutetiensis sp. nov. and of Streptococcus bovis biotype 11.2 as Streptococcus pasteurianus sp. nov.. Int. J. Syst. Evol. Microbiol. 52: 1247–1255.
    pubmed: 12148636
  27. Ricaboni D., Mailhe M., Cadoret F., Vitton V., Fournier P.E., Raoult D.. ‘Colidextribacter massiliensis’ gen. nov., sp. nov., isolated from human right colon. New Microbes New Infect. 17: 27–29.
    pmc: PMC5328710pubmed: 28275436
  28. Richards N., Hinch G., Rowe J.. The effect of current grain feeding practices on hindgut starch fermentation and acidosis in the Australian racing Thoroughbred. Aust. Vet. J. 84: 402–407.
    pubmed: 17092327
  29. Russell J.B., Robinson P.H.. Compositions and characteristics of strains of Streptococcus bovis. J. Dairy Sci. 67: 1525–1531.
    pubmed: 6205028
  30. Schlegel L., Grimont F., Collins M.D., Régnault B., Grimont P.A., Bouvet A.. Streptococcus infantarius sp. nov., Streptococcus infantarius subsp. infantarius subsp. nov. and Streptococcus infantarius subsp. coli subsp. nov., isolated from humans and food. Int. J. Syst. Evol. Microbiol. 50: 1425–1434.
    pubmed: 10939646
  31. Schlegel L., Grimont F., Ageron E., Grimont P.A.D., Bouvet A.. Reappraisal of the taxonomy of the Streptococcus bovis/Streptococcus equinus complex and related species: description of Streptococcus gallolyticus subsp. gallolyticus subsp. nov., S. gallolyticus subsp. macedonicus subsp. nov. and S. gallolyticus subsp. pasteurianus subsp. nov.. Int. J. Syst. Evol. Microbiol. 53: 631–645.
    pubmed: 12807180
  32. Seshadri R., Leahy S.C., Attwood G.T., Teh K.H., Lambie S.C., Cookson A.L., Eloe-Fadrosh E.A., Pavlopoulos G.A., Hadjithomas M., Varghese N.J., Paez-Espino D., Perry R., Henderson G., Creevey C.J., Terrapon N., Lapebie P., Drula E., Lombard V., Rubin E., Kyrpides N.C., Henrissat B., Woyke T., Ivanova N.N., Kelly W.J., Hungate1000 project collaborators. Cultivation and sequencing of rumen microbiome members from the Hungate1000 Collection. Nat. Biotechnol. 36: 359–367.
    pmc: PMC6118326pubmed: 29553575
  33. Yu Z., Morrison M.. Improved extraction of PCR-quality community DNA from digesta and fecal samples. Biotechniques 36: 808–812.
    pubmed: 15152600
  34. Zakrzewski M., Proietti C., Ellis J.J., Hasan S., Brion M.J., Berger B., Krause L.. Calypso: a user-friendly web-server for mining and visualizing microbiome-environment interactions. Bioinformatics 33: 782–783.
    pmc: PMC5408814pubmed: 28025202
  35. Zeyner A., Geissler C., Dittrich A.. Effects of hay intake and feeding sequence on variables in faeces and faecal water (dry matter, pH value, organic acids, ammonia, buffering capacity) of horses. J. Anim. Physiol. Anim. Nutr. (Berl.) 88: 7–19.
    pubmed: 19774758

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