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Comprehensive Genomic Investigation of Coevolution of mcr genes in Escherichia coli Strains via Nanopore Sequencing

Horizontal gene transfer facilitates the spread of antibiotic resistance genes, which constitutes a global challenge. However, the evolutionary trajectory of the mobile colistin resistome in bacteria is largely unknown. To investigate the coevolution and fitness cost of the colistin resistance genes...

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Autores principales: Li, Ruichao, Du, Pengcheng, Zhang, Pei, Li, Yan, Yang, Xiaorong, Wang, Zhiqiang, Wang, Juan, Bai, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7933819/
https://www.ncbi.nlm.nih.gov/pubmed/33728052
http://dx.doi.org/10.1002/gch2.202000014
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author Li, Ruichao
Du, Pengcheng
Zhang, Pei
Li, Yan
Yang, Xiaorong
Wang, Zhiqiang
Wang, Juan
Bai, Li
author_facet Li, Ruichao
Du, Pengcheng
Zhang, Pei
Li, Yan
Yang, Xiaorong
Wang, Zhiqiang
Wang, Juan
Bai, Li
author_sort Li, Ruichao
collection PubMed
description Horizontal gene transfer facilitates the spread of antibiotic resistance genes, which constitutes a global challenge. However, the evolutionary trajectory of the mobile colistin resistome in bacteria is largely unknown. To investigate the coevolution and fitness cost of the colistin resistance genes in wild strains, different assays to uncover the genomic dynamics of mcr‐1 and mcr‐3 in bacterial populations are utilized. Escherichia coli strains harboring both mcr‐1 and mcr‐3.1/3.5 are isolated and mcr genes are associated with diverse mobile elements. Under exposure to colistin, the mcr‐1‐bearing resistome is stably inherited during bacterial replication, but mcr‐3 is prone to be eliminated in populations of certain strains. In the absence of colistin, the persistence rates of the mcr‐1 and mcr‐3‐bearing subclones varies depending on the genomic background. The decay of the mcr‐bearing bacterial populations can be mediated by the elimination of mcr‐containing segments, large genomic deletions, and plasmid loss. Mobile elements, including plasmids and transposons, are double‐edged swords in the evolution of the resistome. The findings support the idea that antibiotic overuse accounts for global spread of multidrug‐resistant (MDR) bacteria. Therefore, stringent regulation of antibiotic prescription for humans and animals should be performed systematically to alleviate the threat of MDR bacteria.
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spelling pubmed-79338192021-03-15 Comprehensive Genomic Investigation of Coevolution of mcr genes in Escherichia coli Strains via Nanopore Sequencing Li, Ruichao Du, Pengcheng Zhang, Pei Li, Yan Yang, Xiaorong Wang, Zhiqiang Wang, Juan Bai, Li Glob Chall Full Papers Horizontal gene transfer facilitates the spread of antibiotic resistance genes, which constitutes a global challenge. However, the evolutionary trajectory of the mobile colistin resistome in bacteria is largely unknown. To investigate the coevolution and fitness cost of the colistin resistance genes in wild strains, different assays to uncover the genomic dynamics of mcr‐1 and mcr‐3 in bacterial populations are utilized. Escherichia coli strains harboring both mcr‐1 and mcr‐3.1/3.5 are isolated and mcr genes are associated with diverse mobile elements. Under exposure to colistin, the mcr‐1‐bearing resistome is stably inherited during bacterial replication, but mcr‐3 is prone to be eliminated in populations of certain strains. In the absence of colistin, the persistence rates of the mcr‐1 and mcr‐3‐bearing subclones varies depending on the genomic background. The decay of the mcr‐bearing bacterial populations can be mediated by the elimination of mcr‐containing segments, large genomic deletions, and plasmid loss. Mobile elements, including plasmids and transposons, are double‐edged swords in the evolution of the resistome. The findings support the idea that antibiotic overuse accounts for global spread of multidrug‐resistant (MDR) bacteria. Therefore, stringent regulation of antibiotic prescription for humans and animals should be performed systematically to alleviate the threat of MDR bacteria. John Wiley and Sons Inc. 2021-01-12 /pmc/articles/PMC7933819/ /pubmed/33728052 http://dx.doi.org/10.1002/gch2.202000014 Text en © 2021 The Authors. Global Challenges published by Wiley‐VCH GmbH 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 Full Papers
Li, Ruichao
Du, Pengcheng
Zhang, Pei
Li, Yan
Yang, Xiaorong
Wang, Zhiqiang
Wang, Juan
Bai, Li
Comprehensive Genomic Investigation of Coevolution of mcr genes in Escherichia coli Strains via Nanopore Sequencing
title Comprehensive Genomic Investigation of Coevolution of mcr genes in Escherichia coli Strains via Nanopore Sequencing
title_full Comprehensive Genomic Investigation of Coevolution of mcr genes in Escherichia coli Strains via Nanopore Sequencing
title_fullStr Comprehensive Genomic Investigation of Coevolution of mcr genes in Escherichia coli Strains via Nanopore Sequencing
title_full_unstemmed Comprehensive Genomic Investigation of Coevolution of mcr genes in Escherichia coli Strains via Nanopore Sequencing
title_short Comprehensive Genomic Investigation of Coevolution of mcr genes in Escherichia coli Strains via Nanopore Sequencing
title_sort comprehensive genomic investigation of coevolution of mcr genes in escherichia coli strains via nanopore sequencing
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7933819/
https://www.ncbi.nlm.nih.gov/pubmed/33728052
http://dx.doi.org/10.1002/gch2.202000014
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