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Novel Variant of New Delhi Metallo-β-lactamase, NDM-20, in Escherichia coli
The spread of carbapenem-resistant Enterobacteriaceae (CRE) mediated by New Delhi metallo-β-lactamase (NDM) poses a serious challenge to clinicians and has become a major public health concern. NDM has been evolving into variants that possess different hydrolysis activity toward antibiotics, so as t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5826333/ https://www.ncbi.nlm.nih.gov/pubmed/29515538 http://dx.doi.org/10.3389/fmicb.2018.00248 |
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author | Liu, Zhihai Li, Jiyun Wang, Xiaoming Liu, Dejun Ke, Yuebin Wang, Yang Shen, Jianzhong |
author_facet | Liu, Zhihai Li, Jiyun Wang, Xiaoming Liu, Dejun Ke, Yuebin Wang, Yang Shen, Jianzhong |
author_sort | Liu, Zhihai |
collection | PubMed |
description | The spread of carbapenem-resistant Enterobacteriaceae (CRE) mediated by New Delhi metallo-β-lactamase (NDM) poses a serious challenge to clinicians and has become a major public health concern. NDM has been evolving into variants that possess different hydrolysis activity toward antibiotics, so as to affect treatment strategy. In addition, very few studies on NDM variants have focused on animal-derived bacterial isolates. Our study reports a novel NDM variant, NDM-20, in an isolate of Escherichia coli CCD1 recovered from the food animal swine in China. The isolate that was assigned to ST1114, exhibited high level resistance to all β-lactams tested, including aztreonam and carbapenems. The gene of bla(NDM-20) was located on an IncX3-type plasmid, surrounded by multiple insertion sequences. Sequencing analysis demonstrated that bla(NDM-20) contained three point mutations at positions 262 (G→T), 460 (A→C), and 809 (G→A), compared with bla(NDM-1), and just one point mutation at position 809 (G→A), relative to bla(NDM-5). Functional analysis revealed that the bla(NDM-20) transformant, DH5α+pHSG398/NDM-20, exhibited a higher resistance to ertapenem than that of bla(NDM-1) transformant DH5α+pHSG398/NDM-1. Kinetic parameter analysis showed that NDM-20 had increased enzymatic activity against some penicillins and cephalosporins but decreased carbapenemase activity relative to NDM-5. The identification of NDM-20 further confirms the evolution and prevalence of NDM variants in bacteria of food-animal origin. |
format | Online Article Text |
id | pubmed-5826333 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58263332018-03-07 Novel Variant of New Delhi Metallo-β-lactamase, NDM-20, in Escherichia coli Liu, Zhihai Li, Jiyun Wang, Xiaoming Liu, Dejun Ke, Yuebin Wang, Yang Shen, Jianzhong Front Microbiol Microbiology The spread of carbapenem-resistant Enterobacteriaceae (CRE) mediated by New Delhi metallo-β-lactamase (NDM) poses a serious challenge to clinicians and has become a major public health concern. NDM has been evolving into variants that possess different hydrolysis activity toward antibiotics, so as to affect treatment strategy. In addition, very few studies on NDM variants have focused on animal-derived bacterial isolates. Our study reports a novel NDM variant, NDM-20, in an isolate of Escherichia coli CCD1 recovered from the food animal swine in China. The isolate that was assigned to ST1114, exhibited high level resistance to all β-lactams tested, including aztreonam and carbapenems. The gene of bla(NDM-20) was located on an IncX3-type plasmid, surrounded by multiple insertion sequences. Sequencing analysis demonstrated that bla(NDM-20) contained three point mutations at positions 262 (G→T), 460 (A→C), and 809 (G→A), compared with bla(NDM-1), and just one point mutation at position 809 (G→A), relative to bla(NDM-5). Functional analysis revealed that the bla(NDM-20) transformant, DH5α+pHSG398/NDM-20, exhibited a higher resistance to ertapenem than that of bla(NDM-1) transformant DH5α+pHSG398/NDM-1. Kinetic parameter analysis showed that NDM-20 had increased enzymatic activity against some penicillins and cephalosporins but decreased carbapenemase activity relative to NDM-5. The identification of NDM-20 further confirms the evolution and prevalence of NDM variants in bacteria of food-animal origin. Frontiers Media S.A. 2018-02-21 /pmc/articles/PMC5826333/ /pubmed/29515538 http://dx.doi.org/10.3389/fmicb.2018.00248 Text en Copyright © 2018 Liu, Li, Wang, Liu, Ke, Wang and Shen. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Liu, Zhihai Li, Jiyun Wang, Xiaoming Liu, Dejun Ke, Yuebin Wang, Yang Shen, Jianzhong Novel Variant of New Delhi Metallo-β-lactamase, NDM-20, in Escherichia coli |
title | Novel Variant of New Delhi Metallo-β-lactamase, NDM-20, in Escherichia coli |
title_full | Novel Variant of New Delhi Metallo-β-lactamase, NDM-20, in Escherichia coli |
title_fullStr | Novel Variant of New Delhi Metallo-β-lactamase, NDM-20, in Escherichia coli |
title_full_unstemmed | Novel Variant of New Delhi Metallo-β-lactamase, NDM-20, in Escherichia coli |
title_short | Novel Variant of New Delhi Metallo-β-lactamase, NDM-20, in Escherichia coli |
title_sort | novel variant of new delhi metallo-β-lactamase, ndm-20, in escherichia coli |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5826333/ https://www.ncbi.nlm.nih.gov/pubmed/29515538 http://dx.doi.org/10.3389/fmicb.2018.00248 |
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