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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...

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Autores principales: Liu, Zhihai, Li, Jiyun, Wang, Xiaoming, Liu, Dejun, Ke, Yuebin, Wang, Yang, Shen, Jianzhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
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.
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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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