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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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2021
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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 |
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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 |
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