Cargando…

First Report of bla(OXA-677) with Enhanced Meropenem-Hydrolyzing Ability in Pseudomonas aeruginosa in China

PURPOSE: OXA-10-type class D β-lactamases have shown their evolutionary potential of enhancing carbapenem resistance. This study aimed to elucidate the role of OXA-10 variants in clinical isolated multidrug resistant (MDR) Pseudomonas aeruginosa and characterize the first appearance of OXA-677 in Ch...

Descripción completa

Detalles Bibliográficos
Autores principales: Sun, Yue, Han, Renru, Ding, Li, Yang, Yang, Guo, Yan, Wu, Shi, Hu, Fupin, Yin, Dandan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8725689/
https://www.ncbi.nlm.nih.gov/pubmed/35002263
http://dx.doi.org/10.2147/IDR.S340662
_version_ 1784626166327410688
author Sun, Yue
Han, Renru
Ding, Li
Yang, Yang
Guo, Yan
Wu, Shi
Hu, Fupin
Yin, Dandan
author_facet Sun, Yue
Han, Renru
Ding, Li
Yang, Yang
Guo, Yan
Wu, Shi
Hu, Fupin
Yin, Dandan
author_sort Sun, Yue
collection PubMed
description PURPOSE: OXA-10-type class D β-lactamases have shown their evolutionary potential of enhancing carbapenem resistance. This study aimed to elucidate the role of OXA-10 variants in clinical isolated multidrug resistant (MDR) Pseudomonas aeruginosa and characterize the first appearance of OXA-677 in China. METHODS: Six bla(OXA-10-like)-positive strains were screened by PCR from 41 P. aeruginosa strains, which were resistant to both carbapenems and ceftazidime-avibactam, collected across China in 2018. The minimum inhibitory concentrations (MIC) were determined with the broth microdilution method. The resistance-associated genes and genetic environment were investigated by whole-genome sequencing (WGS). The function and mechanism of OXA-677 β-lactamase were identified by molecular cloning and protein structure modeling. RESULTS: All the bla(OXA-10-like)-positive Pseudomonas aeruginosa were MDR strains. They also had outer membrane porin defects and produced β-lactam resistance gene bla(PER-1,) fluoroquinolone-resistant gene crpP, aminoglycoside-resistance gene aph(3ʹ)-IIb, aph(6)-Id, aacA and aadA, fosfomycin-resistance gene fosA, sulfamethoxazole-resistance gene sul1, and chloramphenicol-resistance gene catB7. All bla(OXA-10) variants were located in a Tn1403-related transposon, containing aacA4-12-bla(OXA-677)-aadA1, aacA4-12-bla(OXA-101)-aadA5, and bla(OXA-246)-aacA3-aadA13 gene cassette arrays, respectively. Notably, the bla(OXA-677) producer showed a high MIC level of meropenem (MIC>64 mg/L). Compared to bla(OXA-10), bla(OXA-677) was found a G-to-T transversion at position 350, leading to a phenylalanine-for-valine substitution in position 117, which is closer to leucine155 in the omega loop of the active site. MIC of meropenem for E. coli DH5α with the recombinant plasmid pHSG398 carrying bla(OXA-677) was elevated by 8 times. CONCLUSION: We speculate that the OXA-10-like enzymes and the decrease of membrane permeability confer carbapenem resistance, and the V117 substitution in OXA-677 might lead to a higher resistance level of meropenem.
format Online
Article
Text
id pubmed-8725689
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Dove
record_format MEDLINE/PubMed
spelling pubmed-87256892022-01-06 First Report of bla(OXA-677) with Enhanced Meropenem-Hydrolyzing Ability in Pseudomonas aeruginosa in China Sun, Yue Han, Renru Ding, Li Yang, Yang Guo, Yan Wu, Shi Hu, Fupin Yin, Dandan Infect Drug Resist Original Research PURPOSE: OXA-10-type class D β-lactamases have shown their evolutionary potential of enhancing carbapenem resistance. This study aimed to elucidate the role of OXA-10 variants in clinical isolated multidrug resistant (MDR) Pseudomonas aeruginosa and characterize the first appearance of OXA-677 in China. METHODS: Six bla(OXA-10-like)-positive strains were screened by PCR from 41 P. aeruginosa strains, which were resistant to both carbapenems and ceftazidime-avibactam, collected across China in 2018. The minimum inhibitory concentrations (MIC) were determined with the broth microdilution method. The resistance-associated genes and genetic environment were investigated by whole-genome sequencing (WGS). The function and mechanism of OXA-677 β-lactamase were identified by molecular cloning and protein structure modeling. RESULTS: All the bla(OXA-10-like)-positive Pseudomonas aeruginosa were MDR strains. They also had outer membrane porin defects and produced β-lactam resistance gene bla(PER-1,) fluoroquinolone-resistant gene crpP, aminoglycoside-resistance gene aph(3ʹ)-IIb, aph(6)-Id, aacA and aadA, fosfomycin-resistance gene fosA, sulfamethoxazole-resistance gene sul1, and chloramphenicol-resistance gene catB7. All bla(OXA-10) variants were located in a Tn1403-related transposon, containing aacA4-12-bla(OXA-677)-aadA1, aacA4-12-bla(OXA-101)-aadA5, and bla(OXA-246)-aacA3-aadA13 gene cassette arrays, respectively. Notably, the bla(OXA-677) producer showed a high MIC level of meropenem (MIC>64 mg/L). Compared to bla(OXA-10), bla(OXA-677) was found a G-to-T transversion at position 350, leading to a phenylalanine-for-valine substitution in position 117, which is closer to leucine155 in the omega loop of the active site. MIC of meropenem for E. coli DH5α with the recombinant plasmid pHSG398 carrying bla(OXA-677) was elevated by 8 times. CONCLUSION: We speculate that the OXA-10-like enzymes and the decrease of membrane permeability confer carbapenem resistance, and the V117 substitution in OXA-677 might lead to a higher resistance level of meropenem. Dove 2021-12-31 /pmc/articles/PMC8725689/ /pubmed/35002263 http://dx.doi.org/10.2147/IDR.S340662 Text en © 2021 Sun et al. https://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/ (https://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 Original Research
Sun, Yue
Han, Renru
Ding, Li
Yang, Yang
Guo, Yan
Wu, Shi
Hu, Fupin
Yin, Dandan
First Report of bla(OXA-677) with Enhanced Meropenem-Hydrolyzing Ability in Pseudomonas aeruginosa in China
title First Report of bla(OXA-677) with Enhanced Meropenem-Hydrolyzing Ability in Pseudomonas aeruginosa in China
title_full First Report of bla(OXA-677) with Enhanced Meropenem-Hydrolyzing Ability in Pseudomonas aeruginosa in China
title_fullStr First Report of bla(OXA-677) with Enhanced Meropenem-Hydrolyzing Ability in Pseudomonas aeruginosa in China
title_full_unstemmed First Report of bla(OXA-677) with Enhanced Meropenem-Hydrolyzing Ability in Pseudomonas aeruginosa in China
title_short First Report of bla(OXA-677) with Enhanced Meropenem-Hydrolyzing Ability in Pseudomonas aeruginosa in China
title_sort first report of bla(oxa-677) with enhanced meropenem-hydrolyzing ability in pseudomonas aeruginosa in china
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8725689/
https://www.ncbi.nlm.nih.gov/pubmed/35002263
http://dx.doi.org/10.2147/IDR.S340662
work_keys_str_mv AT sunyue firstreportofblaoxa677withenhancedmeropenemhydrolyzingabilityinpseudomonasaeruginosainchina
AT hanrenru firstreportofblaoxa677withenhancedmeropenemhydrolyzingabilityinpseudomonasaeruginosainchina
AT dingli firstreportofblaoxa677withenhancedmeropenemhydrolyzingabilityinpseudomonasaeruginosainchina
AT yangyang firstreportofblaoxa677withenhancedmeropenemhydrolyzingabilityinpseudomonasaeruginosainchina
AT guoyan firstreportofblaoxa677withenhancedmeropenemhydrolyzingabilityinpseudomonasaeruginosainchina
AT wushi firstreportofblaoxa677withenhancedmeropenemhydrolyzingabilityinpseudomonasaeruginosainchina
AT hufupin firstreportofblaoxa677withenhancedmeropenemhydrolyzingabilityinpseudomonasaeruginosainchina
AT yindandan firstreportofblaoxa677withenhancedmeropenemhydrolyzingabilityinpseudomonasaeruginosainchina