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Metagenomic and metabolomic analyses reveal the role of gut microbiome-associated metabolites in diarrhea calves

Calf diarrhea is a multifactorial disease that affects the cattle industry and accounts for more than 50% of calf mortality. Although there is evidence of an association between altered gut microbiota and diarrhea, remarkably little is known about the microbial and metabolic mechanisms underlying th...

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Autores principales: Shi, Zhihai, Wang, Yazhou, Yan, Xiangzhou, Ma, Xiaoya, Duan, Anqin, Hassan, Faiz-ul, Wang, Wenjia, Deng, Tingxian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10654109/
https://www.ncbi.nlm.nih.gov/pubmed/37615434
http://dx.doi.org/10.1128/msystems.00582-23
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author Shi, Zhihai
Wang, Yazhou
Yan, Xiangzhou
Ma, Xiaoya
Duan, Anqin
Hassan, Faiz-ul
Wang, Wenjia
Deng, Tingxian
author_facet Shi, Zhihai
Wang, Yazhou
Yan, Xiangzhou
Ma, Xiaoya
Duan, Anqin
Hassan, Faiz-ul
Wang, Wenjia
Deng, Tingxian
author_sort Shi, Zhihai
collection PubMed
description Calf diarrhea is a multifactorial disease that affects the cattle industry and accounts for more than 50% of calf mortality. Although there is evidence of an association between altered gut microbiota and diarrhea, remarkably little is known about the microbial and metabolic mechanisms underlying the link between gut microbiota dysbiosis and the occurrence of calf diarrhea. Here, we performed fecal metagenomic and metabolomic studies on fecal samples from diarrheic and healthy calves of Xia-nan cattle breed. Results revealed that composition of the gut microbiome and metabolome was remarkably altered in diarrheic calves, and gut microbial alterations were associated with diarrhea and linked to the changes in metabolites. Metabolite profiles showed that diarrheic calves exhibited a marked decrease in some purines (adenosine, adenine, 2'-deoxyguanosine, allantoate, deoxyinosine, and deoxyguanosine) and arachidonic acid (prostaglandin F2α and prostaglandin E2) compared to healthy calves. Purine-producing microbial species, including Lactiplantibacillus plantarum, Campylobacter coli, Treponema porcinum, Klebsiella pneumoniae, and Phocaeicola coprophilus, were significantly reduced in diarrheic calves compared to healthy calves, whereas the arachidonic acid-producing species such as Neisseria gonorrhoeae, Staphylococcus aureus, and Clostridiales bacterium exhibited a marked increase. These microbial signatures were closely associated with the metabolic dysbiosis of purine and arachidonic acid in diarrhea calves. Our study showed that gut microbiota-driven metabolic disorders of purine or arachidonic acid were associated with calf diarrhea. The findings prove that altered gut microbiota plays a role in diarrhea pathogenesis and indicate that gut microbiota-targeted therapies could be useful for both prevention and treatment of diarrhea. IMPORTANCE: Calf diarrhea is of great concern to the global dairy industry as it results in significant economic losses due to lower conception rates, reduced milk production, and early culling. Although there is evidence of an association between altered gut microbiota and diarrhea, remarkably little is known about the microbial and metabolic mechanisms underlying the link between gut microbiota dysbiosis and the occurrence of calf diarrhea. Here, we used fecal metagenomic and metabolomic analyses to demonstrate that gut microbiota-driven metabolic disorders of purine or arachidonic acid were associated with calf diarrhea. These altered gut microbiotas play vital roles in diarrhea pathogenesis and indicate that gut microbiota-targeted therapies could be useful for both prevention and treatment of diarrhea.
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spelling pubmed-106541092023-08-24 Metagenomic and metabolomic analyses reveal the role of gut microbiome-associated metabolites in diarrhea calves Shi, Zhihai Wang, Yazhou Yan, Xiangzhou Ma, Xiaoya Duan, Anqin Hassan, Faiz-ul Wang, Wenjia Deng, Tingxian mSystems Research Article Calf diarrhea is a multifactorial disease that affects the cattle industry and accounts for more than 50% of calf mortality. Although there is evidence of an association between altered gut microbiota and diarrhea, remarkably little is known about the microbial and metabolic mechanisms underlying the link between gut microbiota dysbiosis and the occurrence of calf diarrhea. Here, we performed fecal metagenomic and metabolomic studies on fecal samples from diarrheic and healthy calves of Xia-nan cattle breed. Results revealed that composition of the gut microbiome and metabolome was remarkably altered in diarrheic calves, and gut microbial alterations were associated with diarrhea and linked to the changes in metabolites. Metabolite profiles showed that diarrheic calves exhibited a marked decrease in some purines (adenosine, adenine, 2'-deoxyguanosine, allantoate, deoxyinosine, and deoxyguanosine) and arachidonic acid (prostaglandin F2α and prostaglandin E2) compared to healthy calves. Purine-producing microbial species, including Lactiplantibacillus plantarum, Campylobacter coli, Treponema porcinum, Klebsiella pneumoniae, and Phocaeicola coprophilus, were significantly reduced in diarrheic calves compared to healthy calves, whereas the arachidonic acid-producing species such as Neisseria gonorrhoeae, Staphylococcus aureus, and Clostridiales bacterium exhibited a marked increase. These microbial signatures were closely associated with the metabolic dysbiosis of purine and arachidonic acid in diarrhea calves. Our study showed that gut microbiota-driven metabolic disorders of purine or arachidonic acid were associated with calf diarrhea. The findings prove that altered gut microbiota plays a role in diarrhea pathogenesis and indicate that gut microbiota-targeted therapies could be useful for both prevention and treatment of diarrhea. IMPORTANCE: Calf diarrhea is of great concern to the global dairy industry as it results in significant economic losses due to lower conception rates, reduced milk production, and early culling. Although there is evidence of an association between altered gut microbiota and diarrhea, remarkably little is known about the microbial and metabolic mechanisms underlying the link between gut microbiota dysbiosis and the occurrence of calf diarrhea. Here, we used fecal metagenomic and metabolomic analyses to demonstrate that gut microbiota-driven metabolic disorders of purine or arachidonic acid were associated with calf diarrhea. These altered gut microbiotas play vital roles in diarrhea pathogenesis and indicate that gut microbiota-targeted therapies could be useful for both prevention and treatment of diarrhea. American Society for Microbiology 2023-08-24 /pmc/articles/PMC10654109/ /pubmed/37615434 http://dx.doi.org/10.1128/msystems.00582-23 Text en Copyright © 2023 Shi et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Shi, Zhihai
Wang, Yazhou
Yan, Xiangzhou
Ma, Xiaoya
Duan, Anqin
Hassan, Faiz-ul
Wang, Wenjia
Deng, Tingxian
Metagenomic and metabolomic analyses reveal the role of gut microbiome-associated metabolites in diarrhea calves
title Metagenomic and metabolomic analyses reveal the role of gut microbiome-associated metabolites in diarrhea calves
title_full Metagenomic and metabolomic analyses reveal the role of gut microbiome-associated metabolites in diarrhea calves
title_fullStr Metagenomic and metabolomic analyses reveal the role of gut microbiome-associated metabolites in diarrhea calves
title_full_unstemmed Metagenomic and metabolomic analyses reveal the role of gut microbiome-associated metabolites in diarrhea calves
title_short Metagenomic and metabolomic analyses reveal the role of gut microbiome-associated metabolites in diarrhea calves
title_sort metagenomic and metabolomic analyses reveal the role of gut microbiome-associated metabolites in diarrhea calves
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10654109/
https://www.ncbi.nlm.nih.gov/pubmed/37615434
http://dx.doi.org/10.1128/msystems.00582-23
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