Diversity of Acinetobacter baumannii in four French military hospitals, as assessed by multiple locus variable number of tandem repeats analysis.

<h4>Background</h4>Infections by A. calcoaceticus-A. baumannii (ACB) complex isolates represent a serious threat for wounded and burn patients. Three international multidrug-resistant (MDR) clones (EU clone I-III) are responsible for a large proportion of nosocomial infections with A. ba...

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Main Authors: Yolande Hauck, Charles Soler, Patrick Jault, Audrey Mérens, Patrick Gérome, Christine Mac Nab, François Trueba, Laurent Bargues, Hoang Vu Thien, Gilles Vergnaud, Christine Pourcel
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22984530/pdf/?tool=EBI
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author Yolande Hauck
Charles Soler
Patrick Jault
Audrey Mérens
Patrick Gérome
Christine Mac Nab
François Trueba
Laurent Bargues
Hoang Vu Thien
Gilles Vergnaud
Christine Pourcel
author_facet Yolande Hauck
Charles Soler
Patrick Jault
Audrey Mérens
Patrick Gérome
Christine Mac Nab
François Trueba
Laurent Bargues
Hoang Vu Thien
Gilles Vergnaud
Christine Pourcel
author_sort Yolande Hauck
collection DOAJ
description <h4>Background</h4>Infections by A. calcoaceticus-A. baumannii (ACB) complex isolates represent a serious threat for wounded and burn patients. Three international multidrug-resistant (MDR) clones (EU clone I-III) are responsible for a large proportion of nosocomial infections with A. baumannii but other emerging strains with high epidemic potential also occur.<h4>Methodology/principal findings</h4>We automatized a Multiple locus variable number of tandem repeats (VNTR) analysis (MLVA) protocol and used it to investigate the genetic diversity of 136 ACB isolates from four military hospitals and one childrens hospital. Acinetobacter sp other than baumannii isolates represented 22.6% (31/137) with a majority being A. pittii. The genotyping protocol designed for A.baumannii was also efficient to cluster A. pittii isolates. Fifty-five percent of A. baumannii isolates belonged to the two international clones I and II, and we identified new clones which members were found in the different hospitals. Analysis of two CRISPR-cas systems helped define two clonal complexes and provided phylogenetic information to help trace back their emergence.<h4>Conclusions/significance</h4>The increasing occurrence of A. baumannii infections in the hospital calls for measures to rapidly characterize the isolates and identify emerging clones. The automatized MLVA protocol can be the instrument for such surveys. In addition, the investigation of CRISPR/cas systems may give important keys to understand the evolution of some highly successful clonal complexes.
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spelling doaj.art-9327f94584464b02acb43f7944054e962022-12-21T23:41:13ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0179e4459710.1371/journal.pone.0044597Diversity of Acinetobacter baumannii in four French military hospitals, as assessed by multiple locus variable number of tandem repeats analysis.Yolande HauckCharles SolerPatrick JaultAudrey MérensPatrick GéromeChristine Mac NabFrançois TruebaLaurent BarguesHoang Vu ThienGilles VergnaudChristine Pourcel<h4>Background</h4>Infections by A. calcoaceticus-A. baumannii (ACB) complex isolates represent a serious threat for wounded and burn patients. Three international multidrug-resistant (MDR) clones (EU clone I-III) are responsible for a large proportion of nosocomial infections with A. baumannii but other emerging strains with high epidemic potential also occur.<h4>Methodology/principal findings</h4>We automatized a Multiple locus variable number of tandem repeats (VNTR) analysis (MLVA) protocol and used it to investigate the genetic diversity of 136 ACB isolates from four military hospitals and one childrens hospital. Acinetobacter sp other than baumannii isolates represented 22.6% (31/137) with a majority being A. pittii. The genotyping protocol designed for A.baumannii was also efficient to cluster A. pittii isolates. Fifty-five percent of A. baumannii isolates belonged to the two international clones I and II, and we identified new clones which members were found in the different hospitals. Analysis of two CRISPR-cas systems helped define two clonal complexes and provided phylogenetic information to help trace back their emergence.<h4>Conclusions/significance</h4>The increasing occurrence of A. baumannii infections in the hospital calls for measures to rapidly characterize the isolates and identify emerging clones. The automatized MLVA protocol can be the instrument for such surveys. In addition, the investigation of CRISPR/cas systems may give important keys to understand the evolution of some highly successful clonal complexes.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22984530/pdf/?tool=EBI
spellingShingle Yolande Hauck
Charles Soler
Patrick Jault
Audrey Mérens
Patrick Gérome
Christine Mac Nab
François Trueba
Laurent Bargues
Hoang Vu Thien
Gilles Vergnaud
Christine Pourcel
Diversity of Acinetobacter baumannii in four French military hospitals, as assessed by multiple locus variable number of tandem repeats analysis.
PLoS ONE
title Diversity of Acinetobacter baumannii in four French military hospitals, as assessed by multiple locus variable number of tandem repeats analysis.
title_full Diversity of Acinetobacter baumannii in four French military hospitals, as assessed by multiple locus variable number of tandem repeats analysis.
title_fullStr Diversity of Acinetobacter baumannii in four French military hospitals, as assessed by multiple locus variable number of tandem repeats analysis.
title_full_unstemmed Diversity of Acinetobacter baumannii in four French military hospitals, as assessed by multiple locus variable number of tandem repeats analysis.
title_short Diversity of Acinetobacter baumannii in four French military hospitals, as assessed by multiple locus variable number of tandem repeats analysis.
title_sort diversity of acinetobacter baumannii in four french military hospitals as assessed by multiple locus variable number of tandem repeats analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22984530/pdf/?tool=EBI
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