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Multidrug-resistant bacteria as intestinal colonizers and evolution of intestinal colonization in healthy university students in Portugal

Multidrug-resistant bacteria have been increasingly described in healthcare institutions, however community resistance also seems to be emerging. Escherichia coli an intestinal commensal bacteria, is also a pathogen and represents an important intestinal reservoir of resistance. Our aim was the stud...

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Autores principales: Mota, Raquel, Pinto, Marisa, Palmeira, Josman, Gonçalves, Daniela, Ferreira, Helena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Microbiology Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8115976/
https://www.ncbi.nlm.nih.gov/pubmed/33997613
http://dx.doi.org/10.1099/acmi.0.000182
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author Mota, Raquel
Pinto, Marisa
Palmeira, Josman
Gonçalves, Daniela
Ferreira, Helena
author_facet Mota, Raquel
Pinto, Marisa
Palmeira, Josman
Gonçalves, Daniela
Ferreira, Helena
author_sort Mota, Raquel
collection PubMed
description Multidrug-resistant bacteria have been increasingly described in healthcare institutions, however community resistance also seems to be emerging. Escherichia coli an intestinal commensal bacteria, is also a pathogen and represents an important intestinal reservoir of resistance. Our aim was the study of the intestinal colonization and of the persistence of antibiotic resistant intestinal bacteria in healthy university students of Porto, in the north of Portugal. Samples from 30 university students were collected and analysed. Two E. coli isolates were randomly obtained from each student and Gram-negative bacilli resistant to antibiotics were studied. In addition, we evaluated changes in the Gram-negative intestinal colonization of ten university students in a short period of time. Molecular characterization showed a high presence of bla (TEM) in commensal E. coli . Gram-negative bacteria with intrinsic and extrinsic resistance were isolated, namely Pseudomonas spp., Enterobacter spp. and Pantoea spp. We isolated three ESBL-producing E. coli from two students. These isolates showed bla (CTX-M) group 1 (n=1), bla (CTX-M) group 9 (n=2), bla (TEM) (n=2), bla (SHV) (n=1) and tetA (n=2) genes. Additionally, they showed specific virulence factors and conjugational transfer of antibiotic resistance and virulence genes. One Pseudomonas spp. isolate resistant to carbapenems was detected colonizing one student. Our results confirm that healthy young adults may be colonized with commensals showing clinically relevant antibiotic resistance mechanisms, creating a risk of silent spread of these bacteria in the community.
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spelling pubmed-81159762021-05-13 Multidrug-resistant bacteria as intestinal colonizers and evolution of intestinal colonization in healthy university students in Portugal Mota, Raquel Pinto, Marisa Palmeira, Josman Gonçalves, Daniela Ferreira, Helena Access Microbiol Research Article Multidrug-resistant bacteria have been increasingly described in healthcare institutions, however community resistance also seems to be emerging. Escherichia coli an intestinal commensal bacteria, is also a pathogen and represents an important intestinal reservoir of resistance. Our aim was the study of the intestinal colonization and of the persistence of antibiotic resistant intestinal bacteria in healthy university students of Porto, in the north of Portugal. Samples from 30 university students were collected and analysed. Two E. coli isolates were randomly obtained from each student and Gram-negative bacilli resistant to antibiotics were studied. In addition, we evaluated changes in the Gram-negative intestinal colonization of ten university students in a short period of time. Molecular characterization showed a high presence of bla (TEM) in commensal E. coli . Gram-negative bacteria with intrinsic and extrinsic resistance were isolated, namely Pseudomonas spp., Enterobacter spp. and Pantoea spp. We isolated three ESBL-producing E. coli from two students. These isolates showed bla (CTX-M) group 1 (n=1), bla (CTX-M) group 9 (n=2), bla (TEM) (n=2), bla (SHV) (n=1) and tetA (n=2) genes. Additionally, they showed specific virulence factors and conjugational transfer of antibiotic resistance and virulence genes. One Pseudomonas spp. isolate resistant to carbapenems was detected colonizing one student. Our results confirm that healthy young adults may be colonized with commensals showing clinically relevant antibiotic resistance mechanisms, creating a risk of silent spread of these bacteria in the community. Microbiology Society 2020-11-25 /pmc/articles/PMC8115976/ /pubmed/33997613 http://dx.doi.org/10.1099/acmi.0.000182 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution NonCommercial License.
spellingShingle Research Article
Mota, Raquel
Pinto, Marisa
Palmeira, Josman
Gonçalves, Daniela
Ferreira, Helena
Multidrug-resistant bacteria as intestinal colonizers and evolution of intestinal colonization in healthy university students in Portugal
title Multidrug-resistant bacteria as intestinal colonizers and evolution of intestinal colonization in healthy university students in Portugal
title_full Multidrug-resistant bacteria as intestinal colonizers and evolution of intestinal colonization in healthy university students in Portugal
title_fullStr Multidrug-resistant bacteria as intestinal colonizers and evolution of intestinal colonization in healthy university students in Portugal
title_full_unstemmed Multidrug-resistant bacteria as intestinal colonizers and evolution of intestinal colonization in healthy university students in Portugal
title_short Multidrug-resistant bacteria as intestinal colonizers and evolution of intestinal colonization in healthy university students in Portugal
title_sort multidrug-resistant bacteria as intestinal colonizers and evolution of intestinal colonization in healthy university students in portugal
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8115976/
https://www.ncbi.nlm.nih.gov/pubmed/33997613
http://dx.doi.org/10.1099/acmi.0.000182
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