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Metagenomic Characterization of Intestinal Regions in Pigs With Contrasting Feed Efficiency

Greater feed efficiency (FE) is critical in increasing profitability while reducing the environmental impact of pig production. Previous studies that identified swine FE-associated bacterial taxa were limited in either sampling sites or sequencing methods. This study characterized the microbiomes wi...

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Autores principales: Quan, Jianping, Wu, Zhenfang, Ye, Yong, Peng, Longlong, Wu, Jie, Ruan, Donglin, Qiu, Yibin, Ding, Rongrong, Wang, Xingwang, Zheng, Enqin, Cai, Gengyuan, Huang, Wen, Yang, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6989599/
https://www.ncbi.nlm.nih.gov/pubmed/32038603
http://dx.doi.org/10.3389/fmicb.2020.00032
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author Quan, Jianping
Wu, Zhenfang
Ye, Yong
Peng, Longlong
Wu, Jie
Ruan, Donglin
Qiu, Yibin
Ding, Rongrong
Wang, Xingwang
Zheng, Enqin
Cai, Gengyuan
Huang, Wen
Yang, Jie
author_facet Quan, Jianping
Wu, Zhenfang
Ye, Yong
Peng, Longlong
Wu, Jie
Ruan, Donglin
Qiu, Yibin
Ding, Rongrong
Wang, Xingwang
Zheng, Enqin
Cai, Gengyuan
Huang, Wen
Yang, Jie
author_sort Quan, Jianping
collection PubMed
description Greater feed efficiency (FE) is critical in increasing profitability while reducing the environmental impact of pig production. Previous studies that identified swine FE-associated bacterial taxa were limited in either sampling sites or sequencing methods. This study characterized the microbiomes within the intestine of FE contrasting Duroc × (Landrace × Yorkshire) (DLY) pigs with a comprehensive representation of diverse sampling sites (ileum, cecum, and colon) and a metagenomic sequencing approach. A total of 226 pigs were ranked according to their FE between weaning to 140 day old, and six with extreme phenotypes were selected, three for each of the high and low groups. The results revealed that the cecum and colon had similar microbial taxonomic composition and function, and had higher capacity in polysaccharide metabolism than the ileum. We found in cecum that the high FE pigs had slightly higher richness and evenness in their micriobiota than the low FE pigs. We identified 12 phyla, 17 genera, and 39 species (e.g., Treponema porcinum, Treponema bryantii, and Firmicutes bacterium CAG:110) that were potentially associated with swine FE variation in cecum microbiota through LEfSe analysis. Species enriched in the cecum of the high FE pigs had a greater ability to utilize dietary polysaccharides and dietary protein according to the KEGG annotation. Analysis of antibiotic resistance based on the CARD database annotation indicated that the macB resistant gene might play an important role in shaping the microbial community in the cecum of pigs with contrasting FE. The bacteria from the genus Prevotella was highly enriched in the cecum of low FE pigs, which may impair the establishment of a more effective nutrient harvesting microbiota because of the interaction between Prevotella and other benefical microbes. These findings improved our understanding of the microbial compositions in the different gut locations of DLY pigs and identified many biomarkers associated with FE variation wich may be used to develop strategies to improve FE in pigs.
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spelling pubmed-69895992020-02-07 Metagenomic Characterization of Intestinal Regions in Pigs With Contrasting Feed Efficiency Quan, Jianping Wu, Zhenfang Ye, Yong Peng, Longlong Wu, Jie Ruan, Donglin Qiu, Yibin Ding, Rongrong Wang, Xingwang Zheng, Enqin Cai, Gengyuan Huang, Wen Yang, Jie Front Microbiol Microbiology Greater feed efficiency (FE) is critical in increasing profitability while reducing the environmental impact of pig production. Previous studies that identified swine FE-associated bacterial taxa were limited in either sampling sites or sequencing methods. This study characterized the microbiomes within the intestine of FE contrasting Duroc × (Landrace × Yorkshire) (DLY) pigs with a comprehensive representation of diverse sampling sites (ileum, cecum, and colon) and a metagenomic sequencing approach. A total of 226 pigs were ranked according to their FE between weaning to 140 day old, and six with extreme phenotypes were selected, three for each of the high and low groups. The results revealed that the cecum and colon had similar microbial taxonomic composition and function, and had higher capacity in polysaccharide metabolism than the ileum. We found in cecum that the high FE pigs had slightly higher richness and evenness in their micriobiota than the low FE pigs. We identified 12 phyla, 17 genera, and 39 species (e.g., Treponema porcinum, Treponema bryantii, and Firmicutes bacterium CAG:110) that were potentially associated with swine FE variation in cecum microbiota through LEfSe analysis. Species enriched in the cecum of the high FE pigs had a greater ability to utilize dietary polysaccharides and dietary protein according to the KEGG annotation. Analysis of antibiotic resistance based on the CARD database annotation indicated that the macB resistant gene might play an important role in shaping the microbial community in the cecum of pigs with contrasting FE. The bacteria from the genus Prevotella was highly enriched in the cecum of low FE pigs, which may impair the establishment of a more effective nutrient harvesting microbiota because of the interaction between Prevotella and other benefical microbes. These findings improved our understanding of the microbial compositions in the different gut locations of DLY pigs and identified many biomarkers associated with FE variation wich may be used to develop strategies to improve FE in pigs. Frontiers Media S.A. 2020-01-23 /pmc/articles/PMC6989599/ /pubmed/32038603 http://dx.doi.org/10.3389/fmicb.2020.00032 Text en Copyright © 2020 Quan, Wu, Ye, Peng, Wu, Ruan, Qiu, Ding, Wang, Zheng, Cai, Huang and Yang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Quan, Jianping
Wu, Zhenfang
Ye, Yong
Peng, Longlong
Wu, Jie
Ruan, Donglin
Qiu, Yibin
Ding, Rongrong
Wang, Xingwang
Zheng, Enqin
Cai, Gengyuan
Huang, Wen
Yang, Jie
Metagenomic Characterization of Intestinal Regions in Pigs With Contrasting Feed Efficiency
title Metagenomic Characterization of Intestinal Regions in Pigs With Contrasting Feed Efficiency
title_full Metagenomic Characterization of Intestinal Regions in Pigs With Contrasting Feed Efficiency
title_fullStr Metagenomic Characterization of Intestinal Regions in Pigs With Contrasting Feed Efficiency
title_full_unstemmed Metagenomic Characterization of Intestinal Regions in Pigs With Contrasting Feed Efficiency
title_short Metagenomic Characterization of Intestinal Regions in Pigs With Contrasting Feed Efficiency
title_sort metagenomic characterization of intestinal regions in pigs with contrasting feed efficiency
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6989599/
https://www.ncbi.nlm.nih.gov/pubmed/32038603
http://dx.doi.org/10.3389/fmicb.2020.00032
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