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Geographic pattern of antibiotic resistance genes in the metagenomes of the giant panda

The rise in infections by antibiotic‐resistant bacteria poses a serious public health problem worldwide. The gut microbiome of animals is a reservoir for antibiotic resistance genes (ARGs). However, the correlation between the gut microbiome of wild animals and ARGs remains controversial. Here, base...

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Autores principales: Hu, Ting, Dai, Qinlong, Chen, Hua, Zhang, Zheng, Dai, Qiang, Gu, Xiaodong, Yang, Xuyu, Yang, Zhisong, Zhu, Lifeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7888472/
https://www.ncbi.nlm.nih.gov/pubmed/32812361
http://dx.doi.org/10.1111/1751-7915.13655
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author Hu, Ting
Dai, Qinlong
Chen, Hua
Zhang, Zheng
Dai, Qiang
Gu, Xiaodong
Yang, Xuyu
Yang, Zhisong
Zhu, Lifeng
author_facet Hu, Ting
Dai, Qinlong
Chen, Hua
Zhang, Zheng
Dai, Qiang
Gu, Xiaodong
Yang, Xuyu
Yang, Zhisong
Zhu, Lifeng
author_sort Hu, Ting
collection PubMed
description The rise in infections by antibiotic‐resistant bacteria poses a serious public health problem worldwide. The gut microbiome of animals is a reservoir for antibiotic resistance genes (ARGs). However, the correlation between the gut microbiome of wild animals and ARGs remains controversial. Here, based on the metagenomes of giant pandas (including three wild populations from the Qinling, Qionglai and Xiaoxiangling Mountains, and two major captive populations from Yaan and Chengdu), we investigated the potential correlation between the constitution of the gut microbiome and the composition of ARGs across the different geographic locations and living environments. We found that the types of ARGs were correlated with gut microbiome composition. The NMDS cluster analysis using Jaccard distance of the ARGs composition of the gut microbiome of wild giant pandas displayed a difference based on geographic location. Captivity also had an effect on the differences in ARGs composition. Furthermore, we found that the Qinling population exhibited profound dissimilarities of both gut microbiome composition and ARGs (the highest proportion of Clostridium and vancomycin resistance genes) when compared to the other wild and captive populations studies, which was supported by previous giant panda whole‐genome sequencing analysis. In this study, we provide an example of a potential consensus pattern regarding host population genetics, symbiotic gut microbiome and ARGs. We revealed that habitat isolation impacts the ARG structure in the gut microbiome of mammals. Therefore, the difference in ARG composition between giant panda populations will provide some basic information for their conservation and management, especially for captive populations.
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spelling pubmed-78884722021-02-26 Geographic pattern of antibiotic resistance genes in the metagenomes of the giant panda Hu, Ting Dai, Qinlong Chen, Hua Zhang, Zheng Dai, Qiang Gu, Xiaodong Yang, Xuyu Yang, Zhisong Zhu, Lifeng Microb Biotechnol Research Articles The rise in infections by antibiotic‐resistant bacteria poses a serious public health problem worldwide. The gut microbiome of animals is a reservoir for antibiotic resistance genes (ARGs). However, the correlation between the gut microbiome of wild animals and ARGs remains controversial. Here, based on the metagenomes of giant pandas (including three wild populations from the Qinling, Qionglai and Xiaoxiangling Mountains, and two major captive populations from Yaan and Chengdu), we investigated the potential correlation between the constitution of the gut microbiome and the composition of ARGs across the different geographic locations and living environments. We found that the types of ARGs were correlated with gut microbiome composition. The NMDS cluster analysis using Jaccard distance of the ARGs composition of the gut microbiome of wild giant pandas displayed a difference based on geographic location. Captivity also had an effect on the differences in ARGs composition. Furthermore, we found that the Qinling population exhibited profound dissimilarities of both gut microbiome composition and ARGs (the highest proportion of Clostridium and vancomycin resistance genes) when compared to the other wild and captive populations studies, which was supported by previous giant panda whole‐genome sequencing analysis. In this study, we provide an example of a potential consensus pattern regarding host population genetics, symbiotic gut microbiome and ARGs. We revealed that habitat isolation impacts the ARG structure in the gut microbiome of mammals. Therefore, the difference in ARG composition between giant panda populations will provide some basic information for their conservation and management, especially for captive populations. John Wiley and Sons Inc. 2020-08-18 /pmc/articles/PMC7888472/ /pubmed/32812361 http://dx.doi.org/10.1111/1751-7915.13655 Text en © 2020 The Authors. Microbial Biotechnology published by Society for Applied Microbiology and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Hu, Ting
Dai, Qinlong
Chen, Hua
Zhang, Zheng
Dai, Qiang
Gu, Xiaodong
Yang, Xuyu
Yang, Zhisong
Zhu, Lifeng
Geographic pattern of antibiotic resistance genes in the metagenomes of the giant panda
title Geographic pattern of antibiotic resistance genes in the metagenomes of the giant panda
title_full Geographic pattern of antibiotic resistance genes in the metagenomes of the giant panda
title_fullStr Geographic pattern of antibiotic resistance genes in the metagenomes of the giant panda
title_full_unstemmed Geographic pattern of antibiotic resistance genes in the metagenomes of the giant panda
title_short Geographic pattern of antibiotic resistance genes in the metagenomes of the giant panda
title_sort geographic pattern of antibiotic resistance genes in the metagenomes of the giant panda
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7888472/
https://www.ncbi.nlm.nih.gov/pubmed/32812361
http://dx.doi.org/10.1111/1751-7915.13655
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