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Coexistence Of Plasmid-Mediated mcr-1 And bla(NDM-4) Genes In A Klebsiella pneumoniae Clinical Strain In Vietnam
In this study, we characterized the first clinical Klebsiella pneumoniae strain co- harboring mcr-1 and bla(NDM-4) genes in Vietnam, which was recovered from a patient admitted to hospital in 2015. This strain demonstrated nonsusceptible to all tested antibiotics, including last-line antibiotics suc...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6885539/ https://www.ncbi.nlm.nih.gov/pubmed/31819552 http://dx.doi.org/10.2147/IDR.S226612 |
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author | Le, Lien Tran, Linh Khanh Le-Ha, Tam-Duong Tran, Bich-Phuong Le-Vo, Hong-Ngoc Nguyen, Yen-Nhi Nguyen, Hanh-Lan Hoang-Ngoc, Khanh-Quynh Matsumoto, Yuki Motooka, Daisuke Nakamura, Shota Jones, James W Iida, Tetsuya Cao, Van |
author_facet | Le, Lien Tran, Linh Khanh Le-Ha, Tam-Duong Tran, Bich-Phuong Le-Vo, Hong-Ngoc Nguyen, Yen-Nhi Nguyen, Hanh-Lan Hoang-Ngoc, Khanh-Quynh Matsumoto, Yuki Motooka, Daisuke Nakamura, Shota Jones, James W Iida, Tetsuya Cao, Van |
author_sort | Le, Lien |
collection | PubMed |
description | In this study, we characterized the first clinical Klebsiella pneumoniae strain co- harboring mcr-1 and bla(NDM-4) genes in Vietnam, which was recovered from a patient admitted to hospital in 2015. This strain demonstrated nonsusceptible to all tested antibiotics, including last-line antibiotics such as carbapenems (MICs ≥128 μg/mL) and colistin (MIC =32 μg/mL), except tigecycline (MIC =1 μg/mL). Whole-genome analysis using both MinION and MiSeq data revealed that the strain carried 29 resistance genes. Particularly, mcr-1 and bla(NDM-4) genes were carried by different self-conjugative plasmids and able to be transferred to a recipient by conjugation. The colistin resistance of this strain was conferred by mcr-1 and additional chromosomal resistance determinants. Eight amino acid substitutions found in PmrA, PmrB, PmrC, PmrI, and PmrJ, all proteins that are involved in lipopolysaccharide modifications, may be associated with chromosomal colistin resistance. The accumulation of multiple antibiotic resistance mechanisms in this clinical isolate raises alarm on potential spread of extensively drug-resistant K. pneumoniae in healthcare settings. |
format | Online Article Text |
id | pubmed-6885539 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-68855392019-12-09 Coexistence Of Plasmid-Mediated mcr-1 And bla(NDM-4) Genes In A Klebsiella pneumoniae Clinical Strain In Vietnam Le, Lien Tran, Linh Khanh Le-Ha, Tam-Duong Tran, Bich-Phuong Le-Vo, Hong-Ngoc Nguyen, Yen-Nhi Nguyen, Hanh-Lan Hoang-Ngoc, Khanh-Quynh Matsumoto, Yuki Motooka, Daisuke Nakamura, Shota Jones, James W Iida, Tetsuya Cao, Van Infect Drug Resist Short Report In this study, we characterized the first clinical Klebsiella pneumoniae strain co- harboring mcr-1 and bla(NDM-4) genes in Vietnam, which was recovered from a patient admitted to hospital in 2015. This strain demonstrated nonsusceptible to all tested antibiotics, including last-line antibiotics such as carbapenems (MICs ≥128 μg/mL) and colistin (MIC =32 μg/mL), except tigecycline (MIC =1 μg/mL). Whole-genome analysis using both MinION and MiSeq data revealed that the strain carried 29 resistance genes. Particularly, mcr-1 and bla(NDM-4) genes were carried by different self-conjugative plasmids and able to be transferred to a recipient by conjugation. The colistin resistance of this strain was conferred by mcr-1 and additional chromosomal resistance determinants. Eight amino acid substitutions found in PmrA, PmrB, PmrC, PmrI, and PmrJ, all proteins that are involved in lipopolysaccharide modifications, may be associated with chromosomal colistin resistance. The accumulation of multiple antibiotic resistance mechanisms in this clinical isolate raises alarm on potential spread of extensively drug-resistant K. pneumoniae in healthcare settings. Dove 2019-11-27 /pmc/articles/PMC6885539/ /pubmed/31819552 http://dx.doi.org/10.2147/IDR.S226612 Text en © 2019 Le et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Short Report Le, Lien Tran, Linh Khanh Le-Ha, Tam-Duong Tran, Bich-Phuong Le-Vo, Hong-Ngoc Nguyen, Yen-Nhi Nguyen, Hanh-Lan Hoang-Ngoc, Khanh-Quynh Matsumoto, Yuki Motooka, Daisuke Nakamura, Shota Jones, James W Iida, Tetsuya Cao, Van Coexistence Of Plasmid-Mediated mcr-1 And bla(NDM-4) Genes In A Klebsiella pneumoniae Clinical Strain In Vietnam |
title | Coexistence Of Plasmid-Mediated mcr-1 And bla(NDM-4) Genes In A Klebsiella pneumoniae Clinical Strain In Vietnam |
title_full | Coexistence Of Plasmid-Mediated mcr-1 And bla(NDM-4) Genes In A Klebsiella pneumoniae Clinical Strain In Vietnam |
title_fullStr | Coexistence Of Plasmid-Mediated mcr-1 And bla(NDM-4) Genes In A Klebsiella pneumoniae Clinical Strain In Vietnam |
title_full_unstemmed | Coexistence Of Plasmid-Mediated mcr-1 And bla(NDM-4) Genes In A Klebsiella pneumoniae Clinical Strain In Vietnam |
title_short | Coexistence Of Plasmid-Mediated mcr-1 And bla(NDM-4) Genes In A Klebsiella pneumoniae Clinical Strain In Vietnam |
title_sort | coexistence of plasmid-mediated mcr-1 and bla(ndm-4) genes in a klebsiella pneumoniae clinical strain in vietnam |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6885539/ https://www.ncbi.nlm.nih.gov/pubmed/31819552 http://dx.doi.org/10.2147/IDR.S226612 |
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