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β-lactamase-mediated resistance in MDR-Pseudomonas aeruginosa from Qatar

BACKGROUND: The distribution of β-lactam resistance genes in P. aeruginosa is often closely related to the distribution of certain high-risk international clones. We used whole-genome sequencing (WGS) to identify the predominant sequence types (ST) and β-lactamase genes in clinical isolates of multi...

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Autores principales: Sid Ahmed, Mazen A., Khan, Faisal Ahmad, Sultan, Ali A., Söderquist, Bo, Ibrahim, Emad Bashir, Jass, Jana, Omrani, Ali S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7603671/
https://www.ncbi.nlm.nih.gov/pubmed/33131487
http://dx.doi.org/10.1186/s13756-020-00838-y
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author Sid Ahmed, Mazen A.
Khan, Faisal Ahmad
Sultan, Ali A.
Söderquist, Bo
Ibrahim, Emad Bashir
Jass, Jana
Omrani, Ali S.
author_facet Sid Ahmed, Mazen A.
Khan, Faisal Ahmad
Sultan, Ali A.
Söderquist, Bo
Ibrahim, Emad Bashir
Jass, Jana
Omrani, Ali S.
author_sort Sid Ahmed, Mazen A.
collection PubMed
description BACKGROUND: The distribution of β-lactam resistance genes in P. aeruginosa is often closely related to the distribution of certain high-risk international clones. We used whole-genome sequencing (WGS) to identify the predominant sequence types (ST) and β-lactamase genes in clinical isolates of multidrug-resistant (MDR)-P. aeruginosa from Qatar METHODS: Microbiological identification and susceptibility tests were performed by automated BD Phoenix™ system and manual Liofilchem MIC Test Strips. RESULTS: Among 75 MDR-P. aeruginosa isolates; the largest proportions of susceptibility were to ceftazidime-avibactam (n = 36, 48%), followed by ceftolozane-tazobactam (30, 40%), ceftazidime (n = 21, 28%) and aztreonam (n = 16, 21.3%). All isolates possessed Class C and/or Class D β-lactamases (n = 72, 96% each), while metallo-β-lactamases were detected in 20 (26.7%) isolates. Eight (40%) metallo-β-lactamase producers were susceptible to aztreonam and did not produce any concomitant extended-spectrum β-lactamases. High risk ST235 (n = 16, 21.3%), ST357 (n = 8, 10.7%), ST389 and ST1284 (6, 8% each) were most frequent. Nearly all ST235 isolates (15/16; 93.8%) were resistant to all tested β-lactams. CONCLUSION: MDR-P. aeruginosa isolates from Qatar are highly resistant to antipseudomonal β-lactams. High-risk STs are predominant in Qatar and their associated MDR phenotypes are a cause for considerable concern.
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spelling pubmed-76036712020-11-02 β-lactamase-mediated resistance in MDR-Pseudomonas aeruginosa from Qatar Sid Ahmed, Mazen A. Khan, Faisal Ahmad Sultan, Ali A. Söderquist, Bo Ibrahim, Emad Bashir Jass, Jana Omrani, Ali S. Antimicrob Resist Infect Control Short Report BACKGROUND: The distribution of β-lactam resistance genes in P. aeruginosa is often closely related to the distribution of certain high-risk international clones. We used whole-genome sequencing (WGS) to identify the predominant sequence types (ST) and β-lactamase genes in clinical isolates of multidrug-resistant (MDR)-P. aeruginosa from Qatar METHODS: Microbiological identification and susceptibility tests were performed by automated BD Phoenix™ system and manual Liofilchem MIC Test Strips. RESULTS: Among 75 MDR-P. aeruginosa isolates; the largest proportions of susceptibility were to ceftazidime-avibactam (n = 36, 48%), followed by ceftolozane-tazobactam (30, 40%), ceftazidime (n = 21, 28%) and aztreonam (n = 16, 21.3%). All isolates possessed Class C and/or Class D β-lactamases (n = 72, 96% each), while metallo-β-lactamases were detected in 20 (26.7%) isolates. Eight (40%) metallo-β-lactamase producers were susceptible to aztreonam and did not produce any concomitant extended-spectrum β-lactamases. High risk ST235 (n = 16, 21.3%), ST357 (n = 8, 10.7%), ST389 and ST1284 (6, 8% each) were most frequent. Nearly all ST235 isolates (15/16; 93.8%) were resistant to all tested β-lactams. CONCLUSION: MDR-P. aeruginosa isolates from Qatar are highly resistant to antipseudomonal β-lactams. High-risk STs are predominant in Qatar and their associated MDR phenotypes are a cause for considerable concern. BioMed Central 2020-11-01 /pmc/articles/PMC7603671/ /pubmed/33131487 http://dx.doi.org/10.1186/s13756-020-00838-y Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Short Report
Sid Ahmed, Mazen A.
Khan, Faisal Ahmad
Sultan, Ali A.
Söderquist, Bo
Ibrahim, Emad Bashir
Jass, Jana
Omrani, Ali S.
β-lactamase-mediated resistance in MDR-Pseudomonas aeruginosa from Qatar
title β-lactamase-mediated resistance in MDR-Pseudomonas aeruginosa from Qatar
title_full β-lactamase-mediated resistance in MDR-Pseudomonas aeruginosa from Qatar
title_fullStr β-lactamase-mediated resistance in MDR-Pseudomonas aeruginosa from Qatar
title_full_unstemmed β-lactamase-mediated resistance in MDR-Pseudomonas aeruginosa from Qatar
title_short β-lactamase-mediated resistance in MDR-Pseudomonas aeruginosa from Qatar
title_sort β-lactamase-mediated resistance in mdr-pseudomonas aeruginosa from qatar
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7603671/
https://www.ncbi.nlm.nih.gov/pubmed/33131487
http://dx.doi.org/10.1186/s13756-020-00838-y
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