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A tale of two plasmids: contributions of plasmid associated phenotypes to epidemiological success among Shigella
Dissemination of antimicrobial resistance (AMR) genes by horizontal gene transfer (HGT) mediated through plasmids is a major global concern. Genomic epidemiology studies have shown varying success of different AMR plasmids during outbreaks, but the underlying reasons for these differences are unclea...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9346365/ https://www.ncbi.nlm.nih.gov/pubmed/35919999 http://dx.doi.org/10.1098/rspb.2022.0581 |
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author | Malaka De Silva, P. Stenhouse, George E. Blackwell, Grace A. Bengtsson, Rebecca J. Jenkins, Claire Hall, James P. J. Baker, Kate S. |
author_facet | Malaka De Silva, P. Stenhouse, George E. Blackwell, Grace A. Bengtsson, Rebecca J. Jenkins, Claire Hall, James P. J. Baker, Kate S. |
author_sort | Malaka De Silva, P. |
collection | PubMed |
description | Dissemination of antimicrobial resistance (AMR) genes by horizontal gene transfer (HGT) mediated through plasmids is a major global concern. Genomic epidemiology studies have shown varying success of different AMR plasmids during outbreaks, but the underlying reasons for these differences are unclear. Here, we investigated two Shigella plasmids (pKSR100 and pAPR100) that circulated in the same transmission network but had starkly contrasting epidemiological outcomes to identify plasmid features that may have contributed to the differences. We used plasmid comparative genomics to reveal divergence between the two plasmids in genes encoding AMR, SOS response alleviation and conjugation. Experimental analyses revealed that these genomic differences corresponded with reduced conjugation efficiencies for the epidemiologically successful pKSR100, but more extensive AMR, reduced fitness costs, and a reduced SOS response in the presence of antimicrobials, compared with the less successful pAPR100. The discrepant phenotypes between the two plasmids are consistent with the hypothesis that plasmid-associated phenotypes contribute to determining the epidemiological outcome of AMR HGT and suggest that phenotypes relevant in responding to antimicrobial pressure and fitness impact may be more important than those around conjugation in this setting. Plasmid phenotypes could thus be valuable tools in conjunction with genomic epidemiology for predicting AMR dissemination. |
format | Online Article Text |
id | pubmed-9346365 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-93463652022-08-09 A tale of two plasmids: contributions of plasmid associated phenotypes to epidemiological success among Shigella Malaka De Silva, P. Stenhouse, George E. Blackwell, Grace A. Bengtsson, Rebecca J. Jenkins, Claire Hall, James P. J. Baker, Kate S. Proc Biol Sci Genetics and Genomics Dissemination of antimicrobial resistance (AMR) genes by horizontal gene transfer (HGT) mediated through plasmids is a major global concern. Genomic epidemiology studies have shown varying success of different AMR plasmids during outbreaks, but the underlying reasons for these differences are unclear. Here, we investigated two Shigella plasmids (pKSR100 and pAPR100) that circulated in the same transmission network but had starkly contrasting epidemiological outcomes to identify plasmid features that may have contributed to the differences. We used plasmid comparative genomics to reveal divergence between the two plasmids in genes encoding AMR, SOS response alleviation and conjugation. Experimental analyses revealed that these genomic differences corresponded with reduced conjugation efficiencies for the epidemiologically successful pKSR100, but more extensive AMR, reduced fitness costs, and a reduced SOS response in the presence of antimicrobials, compared with the less successful pAPR100. The discrepant phenotypes between the two plasmids are consistent with the hypothesis that plasmid-associated phenotypes contribute to determining the epidemiological outcome of AMR HGT and suggest that phenotypes relevant in responding to antimicrobial pressure and fitness impact may be more important than those around conjugation in this setting. Plasmid phenotypes could thus be valuable tools in conjunction with genomic epidemiology for predicting AMR dissemination. The Royal Society 2022-08-10 2022-08-03 /pmc/articles/PMC9346365/ /pubmed/35919999 http://dx.doi.org/10.1098/rspb.2022.0581 Text en © 2022 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Genetics and Genomics Malaka De Silva, P. Stenhouse, George E. Blackwell, Grace A. Bengtsson, Rebecca J. Jenkins, Claire Hall, James P. J. Baker, Kate S. A tale of two plasmids: contributions of plasmid associated phenotypes to epidemiological success among Shigella |
title | A tale of two plasmids: contributions of plasmid associated phenotypes to epidemiological success among Shigella |
title_full | A tale of two plasmids: contributions of plasmid associated phenotypes to epidemiological success among Shigella |
title_fullStr | A tale of two plasmids: contributions of plasmid associated phenotypes to epidemiological success among Shigella |
title_full_unstemmed | A tale of two plasmids: contributions of plasmid associated phenotypes to epidemiological success among Shigella |
title_short | A tale of two plasmids: contributions of plasmid associated phenotypes to epidemiological success among Shigella |
title_sort | tale of two plasmids: contributions of plasmid associated phenotypes to epidemiological success among shigella |
topic | Genetics and Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9346365/ https://www.ncbi.nlm.nih.gov/pubmed/35919999 http://dx.doi.org/10.1098/rspb.2022.0581 |
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