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Hospital-diagnosed infections with Escherichia coli clonal group ST131 are mostly acquired in the community

The worldwide spread of E. coli ST131 has significantly contributed to the dissemination of E. coli producing extended-spectrum β-lactamases (ESBL). In a French University hospital, we assessed the molecular features of ESBL-producing E. coli and identified risk factors in patients for colonization...

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Autores principales: Muller, Allison, Gbaguidi-Haore, Houssein, Cholley, Pascal, Hocquet, Didier, Sauget, Marlène, Bertrand, Xavier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7952690/
https://www.ncbi.nlm.nih.gov/pubmed/33707589
http://dx.doi.org/10.1038/s41598-021-85116-6
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author Muller, Allison
Gbaguidi-Haore, Houssein
Cholley, Pascal
Hocquet, Didier
Sauget, Marlène
Bertrand, Xavier
author_facet Muller, Allison
Gbaguidi-Haore, Houssein
Cholley, Pascal
Hocquet, Didier
Sauget, Marlène
Bertrand, Xavier
author_sort Muller, Allison
collection PubMed
description The worldwide spread of E. coli ST131 has significantly contributed to the dissemination of E. coli producing extended-spectrum β-lactamases (ESBL). In a French University hospital, we assessed the molecular features of ESBL-producing E. coli and identified risk factors in patients for colonization or infection with E. coli ST131. Over a 2-year period (2015–2017), each patient with at least one clinical isolate or one screening isolate positive with ESBL-producing E. coli were included (n = 491). The ST131 clonal group accounted for 17.5% (n = 86) of all ESBL-producing E. coli and represented 57.3% isolates of phylogroup B2. FimH-based sub-typing showed that 79.1% (68/86) of ST131 isolates were fimH30, among which 67.6% (n = 46), 20.6% (n = 14) and 11.8% (n = 8) isolates harbored genes encoding the ESBL CTX-M-15, CTX-M-27, and CTX-M-14, respectively. The multivariate analysis identified two factors independently associated with ST131 ESBL-producing E. coli isolates: infection (Odds ratio [OR] = 1.887, 95% confidence interval [CI]: 1.143–3.115; p = 0.013) and community acquisition (OR = 2.220, 95% CI: 1.335–3.693; p = 0.002). In conclusion, our study confirmed the predominance of ST131 clonal group among ESBL-producing E. coli and the difficulty to identify common risk factors associated with carriage of this pandemic clonal group.
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spelling pubmed-79526902021-03-15 Hospital-diagnosed infections with Escherichia coli clonal group ST131 are mostly acquired in the community Muller, Allison Gbaguidi-Haore, Houssein Cholley, Pascal Hocquet, Didier Sauget, Marlène Bertrand, Xavier Sci Rep Article The worldwide spread of E. coli ST131 has significantly contributed to the dissemination of E. coli producing extended-spectrum β-lactamases (ESBL). In a French University hospital, we assessed the molecular features of ESBL-producing E. coli and identified risk factors in patients for colonization or infection with E. coli ST131. Over a 2-year period (2015–2017), each patient with at least one clinical isolate or one screening isolate positive with ESBL-producing E. coli were included (n = 491). The ST131 clonal group accounted for 17.5% (n = 86) of all ESBL-producing E. coli and represented 57.3% isolates of phylogroup B2. FimH-based sub-typing showed that 79.1% (68/86) of ST131 isolates were fimH30, among which 67.6% (n = 46), 20.6% (n = 14) and 11.8% (n = 8) isolates harbored genes encoding the ESBL CTX-M-15, CTX-M-27, and CTX-M-14, respectively. The multivariate analysis identified two factors independently associated with ST131 ESBL-producing E. coli isolates: infection (Odds ratio [OR] = 1.887, 95% confidence interval [CI]: 1.143–3.115; p = 0.013) and community acquisition (OR = 2.220, 95% CI: 1.335–3.693; p = 0.002). In conclusion, our study confirmed the predominance of ST131 clonal group among ESBL-producing E. coli and the difficulty to identify common risk factors associated with carriage of this pandemic clonal group. Nature Publishing Group UK 2021-03-11 /pmc/articles/PMC7952690/ /pubmed/33707589 http://dx.doi.org/10.1038/s41598-021-85116-6 Text en © The Author(s) 2021 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/.
spellingShingle Article
Muller, Allison
Gbaguidi-Haore, Houssein
Cholley, Pascal
Hocquet, Didier
Sauget, Marlène
Bertrand, Xavier
Hospital-diagnosed infections with Escherichia coli clonal group ST131 are mostly acquired in the community
title Hospital-diagnosed infections with Escherichia coli clonal group ST131 are mostly acquired in the community
title_full Hospital-diagnosed infections with Escherichia coli clonal group ST131 are mostly acquired in the community
title_fullStr Hospital-diagnosed infections with Escherichia coli clonal group ST131 are mostly acquired in the community
title_full_unstemmed Hospital-diagnosed infections with Escherichia coli clonal group ST131 are mostly acquired in the community
title_short Hospital-diagnosed infections with Escherichia coli clonal group ST131 are mostly acquired in the community
title_sort hospital-diagnosed infections with escherichia coli clonal group st131 are mostly acquired in the community
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7952690/
https://www.ncbi.nlm.nih.gov/pubmed/33707589
http://dx.doi.org/10.1038/s41598-021-85116-6
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