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Resistome of carbapenem- and colistin-resistant Klebsiella pneumoniae clinical isolates
The emergence and dissemination of carbapenemases, bacterial enzymes able to inactivate most β-lactam antibiotics, in Enterobacteriaceae is of increasing concern. The concurrent spread of resistance against colistin, an antibiotic of last resort, further compounds this challenge further. Whole-genom...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5993281/ https://www.ncbi.nlm.nih.gov/pubmed/29883490 http://dx.doi.org/10.1371/journal.pone.0198526 |
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author | Lomonaco, Sara Crawford, Matthew A. Lascols, Christine Timme, Ruth E. Anderson, Kevin Hodge, David R. Fisher, Debra J. Pillai, Segaran P. Morse, Stephen A. Khan, Erum Hughes, Molly A. Allard, Marc W. Sharma, Shashi K. |
author_facet | Lomonaco, Sara Crawford, Matthew A. Lascols, Christine Timme, Ruth E. Anderson, Kevin Hodge, David R. Fisher, Debra J. Pillai, Segaran P. Morse, Stephen A. Khan, Erum Hughes, Molly A. Allard, Marc W. Sharma, Shashi K. |
author_sort | Lomonaco, Sara |
collection | PubMed |
description | The emergence and dissemination of carbapenemases, bacterial enzymes able to inactivate most β-lactam antibiotics, in Enterobacteriaceae is of increasing concern. The concurrent spread of resistance against colistin, an antibiotic of last resort, further compounds this challenge further. Whole-genome sequencing (WGS) can play a significant role in the rapid and accurate detection/characterization of existing and emergent resistance determinants, an essential aspect of public health surveillance and response activities to combat the spread of antimicrobial resistant bacteria. In the current study, WGS data was used to characterize the genomic content of antimicrobial resistance genes, including those encoding carbapenemases, in 10 multidrug-resistant Klebsiella pneumoniae isolates from Pakistan. These clinical isolates represented five sequence types: ST11 (n = 3 isolates), ST14 (n = 3), ST15 (n = 1), ST101 (n = 2), and ST307 (n = 1). Resistance profiles against 25 clinically-relevant antimicrobials were determined by broth microdilution; resistant phenotypes were observed for at least 15 of the 25 antibiotics tested in all isolates except one. Specifically, 8/10 isolates were carbapenem-resistant and 7/10 isolates were colistin-resistant. The bla(NDM-1) and bla(OXA-48) carbapenemase genes were present in 7/10 and 5/10 isolates, respectively; including 2 isolates carrying both genes. No plasmid-mediated determinants for colistin resistance (e.g. mcr) were detected, but disruptions and mutations in chromosomal loci (i.e. mgrB and pmrB) previously reported to confer colistin resistance were observed. A bla(OXA-48)-carrying IncL/M-type plasmid was found in all bla(OXA-48)-positive isolates. The application of WGS to molecular epidemiology and surveillance studies, as exemplified here, will provide both a more complete understanding of the global distribution of MDR isolates and a robust surveillance tool useful for detecting emerging threats to public health. |
format | Online Article Text |
id | pubmed-5993281 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-59932812018-06-15 Resistome of carbapenem- and colistin-resistant Klebsiella pneumoniae clinical isolates Lomonaco, Sara Crawford, Matthew A. Lascols, Christine Timme, Ruth E. Anderson, Kevin Hodge, David R. Fisher, Debra J. Pillai, Segaran P. Morse, Stephen A. Khan, Erum Hughes, Molly A. Allard, Marc W. Sharma, Shashi K. PLoS One Research Article The emergence and dissemination of carbapenemases, bacterial enzymes able to inactivate most β-lactam antibiotics, in Enterobacteriaceae is of increasing concern. The concurrent spread of resistance against colistin, an antibiotic of last resort, further compounds this challenge further. Whole-genome sequencing (WGS) can play a significant role in the rapid and accurate detection/characterization of existing and emergent resistance determinants, an essential aspect of public health surveillance and response activities to combat the spread of antimicrobial resistant bacteria. In the current study, WGS data was used to characterize the genomic content of antimicrobial resistance genes, including those encoding carbapenemases, in 10 multidrug-resistant Klebsiella pneumoniae isolates from Pakistan. These clinical isolates represented five sequence types: ST11 (n = 3 isolates), ST14 (n = 3), ST15 (n = 1), ST101 (n = 2), and ST307 (n = 1). Resistance profiles against 25 clinically-relevant antimicrobials were determined by broth microdilution; resistant phenotypes were observed for at least 15 of the 25 antibiotics tested in all isolates except one. Specifically, 8/10 isolates were carbapenem-resistant and 7/10 isolates were colistin-resistant. The bla(NDM-1) and bla(OXA-48) carbapenemase genes were present in 7/10 and 5/10 isolates, respectively; including 2 isolates carrying both genes. No plasmid-mediated determinants for colistin resistance (e.g. mcr) were detected, but disruptions and mutations in chromosomal loci (i.e. mgrB and pmrB) previously reported to confer colistin resistance were observed. A bla(OXA-48)-carrying IncL/M-type plasmid was found in all bla(OXA-48)-positive isolates. The application of WGS to molecular epidemiology and surveillance studies, as exemplified here, will provide both a more complete understanding of the global distribution of MDR isolates and a robust surveillance tool useful for detecting emerging threats to public health. Public Library of Science 2018-06-08 /pmc/articles/PMC5993281/ /pubmed/29883490 http://dx.doi.org/10.1371/journal.pone.0198526 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Lomonaco, Sara Crawford, Matthew A. Lascols, Christine Timme, Ruth E. Anderson, Kevin Hodge, David R. Fisher, Debra J. Pillai, Segaran P. Morse, Stephen A. Khan, Erum Hughes, Molly A. Allard, Marc W. Sharma, Shashi K. Resistome of carbapenem- and colistin-resistant Klebsiella pneumoniae clinical isolates |
title | Resistome of carbapenem- and colistin-resistant Klebsiella pneumoniae clinical isolates |
title_full | Resistome of carbapenem- and colistin-resistant Klebsiella pneumoniae clinical isolates |
title_fullStr | Resistome of carbapenem- and colistin-resistant Klebsiella pneumoniae clinical isolates |
title_full_unstemmed | Resistome of carbapenem- and colistin-resistant Klebsiella pneumoniae clinical isolates |
title_short | Resistome of carbapenem- and colistin-resistant Klebsiella pneumoniae clinical isolates |
title_sort | resistome of carbapenem- and colistin-resistant klebsiella pneumoniae clinical isolates |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5993281/ https://www.ncbi.nlm.nih.gov/pubmed/29883490 http://dx.doi.org/10.1371/journal.pone.0198526 |
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