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Mutations in porin LamB contribute to ceftazidime-avibactam resistance in KPC-producing Klebsiella pneumoniae

Ceftazidime-avibactam (CAZ-AVI) shows promising activity against carbapenem-resistant Klebsiella pneumoniae (CRKP), however, CAZ-AVI resistance have emerged recently. Mutations in KPCs, porins OmpK35 and/or OmpK36, and PBPs are known to contribute to the resistance to CAZ-AVI in CRKP. To identify no...

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Autores principales: Guo, Yingyi, Liu, Ningjing, Lin, Zhiwei, Ba, Xiaoliang, Zhuo, Chuyue, Li, Feifeng, Wang, Jiong, Li, Yitan, Yao, Likang, Liu, Baomo, Xiao, Shunian, Jiang, Ying, Zhuo, Chao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8567916/
https://www.ncbi.nlm.nih.gov/pubmed/34551677
http://dx.doi.org/10.1080/22221751.2021.1984182
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author Guo, Yingyi
Liu, Ningjing
Lin, Zhiwei
Ba, Xiaoliang
Zhuo, Chuyue
Li, Feifeng
Wang, Jiong
Li, Yitan
Yao, Likang
Liu, Baomo
Xiao, Shunian
Jiang, Ying
Zhuo, Chao
author_facet Guo, Yingyi
Liu, Ningjing
Lin, Zhiwei
Ba, Xiaoliang
Zhuo, Chuyue
Li, Feifeng
Wang, Jiong
Li, Yitan
Yao, Likang
Liu, Baomo
Xiao, Shunian
Jiang, Ying
Zhuo, Chao
author_sort Guo, Yingyi
collection PubMed
description Ceftazidime-avibactam (CAZ-AVI) shows promising activity against carbapenem-resistant Klebsiella pneumoniae (CRKP), however, CAZ-AVI resistance have emerged recently. Mutations in KPCs, porins OmpK35 and/or OmpK36, and PBPs are known to contribute to the resistance to CAZ-AVI in CRKP. To identify novel CAZ-AVI resistance mechanism, we generated 10 CAZ-AVI-resistant strains from 14 CAZ-AVI susceptible KPC-producing K. pneumoniae (KPC-Kp) strains through in vitro multipassage resistance selection using low concentrations of CAZ-AVI. Comparative genomic analysis for the original and derived mutants identified CAZ-AVI resistance-associated mutations in KPCs, PBP3 (encoded by ftsI), and LamB, an outer membrane maltoporin. CAZ-AVI susceptible KPC-Kp strains became resistant when complemented with mutated bla(KPC) genes. Complementation experiments also showed that a plasmid borne copy of wild-type lamB or ftsI gene reduced the MIC value of CAZ-AVI in the induced resistant strains. In addition, bla(KPC) expression level increased in four of the six CAZ-AVI-resistant strains without KPC mutations, indicating a probable association between increased bla(KPC) expression and increased resistance in these strains. In conclusion, we here identified a novel mechanism of CAZ-AVI resistance associated with mutations in porin LamB in KPC-Kp.
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spelling pubmed-85679162021-11-05 Mutations in porin LamB contribute to ceftazidime-avibactam resistance in KPC-producing Klebsiella pneumoniae Guo, Yingyi Liu, Ningjing Lin, Zhiwei Ba, Xiaoliang Zhuo, Chuyue Li, Feifeng Wang, Jiong Li, Yitan Yao, Likang Liu, Baomo Xiao, Shunian Jiang, Ying Zhuo, Chao Emerg Microbes Infect Original Article Ceftazidime-avibactam (CAZ-AVI) shows promising activity against carbapenem-resistant Klebsiella pneumoniae (CRKP), however, CAZ-AVI resistance have emerged recently. Mutations in KPCs, porins OmpK35 and/or OmpK36, and PBPs are known to contribute to the resistance to CAZ-AVI in CRKP. To identify novel CAZ-AVI resistance mechanism, we generated 10 CAZ-AVI-resistant strains from 14 CAZ-AVI susceptible KPC-producing K. pneumoniae (KPC-Kp) strains through in vitro multipassage resistance selection using low concentrations of CAZ-AVI. Comparative genomic analysis for the original and derived mutants identified CAZ-AVI resistance-associated mutations in KPCs, PBP3 (encoded by ftsI), and LamB, an outer membrane maltoporin. CAZ-AVI susceptible KPC-Kp strains became resistant when complemented with mutated bla(KPC) genes. Complementation experiments also showed that a plasmid borne copy of wild-type lamB or ftsI gene reduced the MIC value of CAZ-AVI in the induced resistant strains. In addition, bla(KPC) expression level increased in four of the six CAZ-AVI-resistant strains without KPC mutations, indicating a probable association between increased bla(KPC) expression and increased resistance in these strains. In conclusion, we here identified a novel mechanism of CAZ-AVI resistance associated with mutations in porin LamB in KPC-Kp. Taylor & Francis 2021-11-02 /pmc/articles/PMC8567916/ /pubmed/34551677 http://dx.doi.org/10.1080/22221751.2021.1984182 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group, on behalf of Shanghai Shangyixun Cultural Communication Co., Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed 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, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Guo, Yingyi
Liu, Ningjing
Lin, Zhiwei
Ba, Xiaoliang
Zhuo, Chuyue
Li, Feifeng
Wang, Jiong
Li, Yitan
Yao, Likang
Liu, Baomo
Xiao, Shunian
Jiang, Ying
Zhuo, Chao
Mutations in porin LamB contribute to ceftazidime-avibactam resistance in KPC-producing Klebsiella pneumoniae
title Mutations in porin LamB contribute to ceftazidime-avibactam resistance in KPC-producing Klebsiella pneumoniae
title_full Mutations in porin LamB contribute to ceftazidime-avibactam resistance in KPC-producing Klebsiella pneumoniae
title_fullStr Mutations in porin LamB contribute to ceftazidime-avibactam resistance in KPC-producing Klebsiella pneumoniae
title_full_unstemmed Mutations in porin LamB contribute to ceftazidime-avibactam resistance in KPC-producing Klebsiella pneumoniae
title_short Mutations in porin LamB contribute to ceftazidime-avibactam resistance in KPC-producing Klebsiella pneumoniae
title_sort mutations in porin lamb contribute to ceftazidime-avibactam resistance in kpc-producing klebsiella pneumoniae
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8567916/
https://www.ncbi.nlm.nih.gov/pubmed/34551677
http://dx.doi.org/10.1080/22221751.2021.1984182
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