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Phenotypic and genotypic within-host diversity of Pseudomonas aeruginosa urinary isolates

This study aimed to assess phenotypic and molecular inter-patient and within-host diversity of Pseudomonas aeruginosa isolates responsible for urinary tract infection (UTI) or asymptomatic bacteriuria (AB). Clinical data of 120 consecutive P. aeruginosa UTI (n = 40) and AB (n = 80) were prospectivel...

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Autores principales: Cottalorda, Agnès, Dahyot, Sandrine, Soares, Anaïs, Alexandre, Kevin, Zorgniotti, Isabelle, Etienne, Manuel, Jumas-Bilak, Estelle, Pestel-Caron, Martine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8967880/
https://www.ncbi.nlm.nih.gov/pubmed/35354853
http://dx.doi.org/10.1038/s41598-022-09234-5
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author Cottalorda, Agnès
Dahyot, Sandrine
Soares, Anaïs
Alexandre, Kevin
Zorgniotti, Isabelle
Etienne, Manuel
Jumas-Bilak, Estelle
Pestel-Caron, Martine
author_facet Cottalorda, Agnès
Dahyot, Sandrine
Soares, Anaïs
Alexandre, Kevin
Zorgniotti, Isabelle
Etienne, Manuel
Jumas-Bilak, Estelle
Pestel-Caron, Martine
author_sort Cottalorda, Agnès
collection PubMed
description This study aimed to assess phenotypic and molecular inter-patient and within-host diversity of Pseudomonas aeruginosa isolates responsible for urinary tract infection (UTI) or asymptomatic bacteriuria (AB). Clinical data of 120 consecutive P. aeruginosa UTI (n = 40) and AB (n = 80) were prospectively analyzed. Up to five P. aeruginosa isolates per sample were collected. Antimicrobial susceptibility testing (AST) was determined for all isolates (n = 591); a subset of 358 was characterized by multilocus sequence typing. 444 isolates (75%) were non-multidrug resistant (MDR), 113 (19%) were MDR, and 34 (6%) were extensively drug resistant. A genetically highly diverse population was observed (64 sequence types [STs]), without strict correlation between genotypes and clinical settings. 35 patients (28%; 12 UTIs and 23 ABs) presented distinct antimicrobial resistance (AMR) profiles within a given urine sample, significantly associated with previous carbapenem and fluroquinolones exposure; five of them also exhibited polyclonal UTI or AB (with isolates belonging to two STs). P. aeruginosa urinary isolates of these 120 patients were highly diverse, in terms of AMR as well as genetic background. Both within-host AMR and molecular diversity can complicate AST, treatment and control of P. aeruginosa UTI.
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spelling pubmed-89678802022-04-01 Phenotypic and genotypic within-host diversity of Pseudomonas aeruginosa urinary isolates Cottalorda, Agnès Dahyot, Sandrine Soares, Anaïs Alexandre, Kevin Zorgniotti, Isabelle Etienne, Manuel Jumas-Bilak, Estelle Pestel-Caron, Martine Sci Rep Article This study aimed to assess phenotypic and molecular inter-patient and within-host diversity of Pseudomonas aeruginosa isolates responsible for urinary tract infection (UTI) or asymptomatic bacteriuria (AB). Clinical data of 120 consecutive P. aeruginosa UTI (n = 40) and AB (n = 80) were prospectively analyzed. Up to five P. aeruginosa isolates per sample were collected. Antimicrobial susceptibility testing (AST) was determined for all isolates (n = 591); a subset of 358 was characterized by multilocus sequence typing. 444 isolates (75%) were non-multidrug resistant (MDR), 113 (19%) were MDR, and 34 (6%) were extensively drug resistant. A genetically highly diverse population was observed (64 sequence types [STs]), without strict correlation between genotypes and clinical settings. 35 patients (28%; 12 UTIs and 23 ABs) presented distinct antimicrobial resistance (AMR) profiles within a given urine sample, significantly associated with previous carbapenem and fluroquinolones exposure; five of them also exhibited polyclonal UTI or AB (with isolates belonging to two STs). P. aeruginosa urinary isolates of these 120 patients were highly diverse, in terms of AMR as well as genetic background. Both within-host AMR and molecular diversity can complicate AST, treatment and control of P. aeruginosa UTI. Nature Publishing Group UK 2022-03-30 /pmc/articles/PMC8967880/ /pubmed/35354853 http://dx.doi.org/10.1038/s41598-022-09234-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Cottalorda, Agnès
Dahyot, Sandrine
Soares, Anaïs
Alexandre, Kevin
Zorgniotti, Isabelle
Etienne, Manuel
Jumas-Bilak, Estelle
Pestel-Caron, Martine
Phenotypic and genotypic within-host diversity of Pseudomonas aeruginosa urinary isolates
title Phenotypic and genotypic within-host diversity of Pseudomonas aeruginosa urinary isolates
title_full Phenotypic and genotypic within-host diversity of Pseudomonas aeruginosa urinary isolates
title_fullStr Phenotypic and genotypic within-host diversity of Pseudomonas aeruginosa urinary isolates
title_full_unstemmed Phenotypic and genotypic within-host diversity of Pseudomonas aeruginosa urinary isolates
title_short Phenotypic and genotypic within-host diversity of Pseudomonas aeruginosa urinary isolates
title_sort phenotypic and genotypic within-host diversity of pseudomonas aeruginosa urinary isolates
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8967880/
https://www.ncbi.nlm.nih.gov/pubmed/35354853
http://dx.doi.org/10.1038/s41598-022-09234-5
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