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Pseudomonas aeruginosa Population Structure Revisited

At present there are strong indications that Pseudomonas aeruginosa exhibits an epidemic population structure; clinical isolates are indistinguishable from environmental isolates, and they do not exhibit a specific (disease) habitat selection. However, some important issues, such as the worldwide em...

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Autores principales: Pirnay, Jean-Paul, Bilocq, Florence, Pot, Bruno, Cornelis, Pierre, Zizi, Martin, Van Eldere, Johan, Deschaght, Pieter, Vaneechoutte, Mario, Jennes, Serge, Pitt, Tyrone, De Vos, Daniel
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2777410/
https://www.ncbi.nlm.nih.gov/pubmed/19936230
http://dx.doi.org/10.1371/journal.pone.0007740
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author Pirnay, Jean-Paul
Bilocq, Florence
Pot, Bruno
Cornelis, Pierre
Zizi, Martin
Van Eldere, Johan
Deschaght, Pieter
Vaneechoutte, Mario
Jennes, Serge
Pitt, Tyrone
De Vos, Daniel
author_facet Pirnay, Jean-Paul
Bilocq, Florence
Pot, Bruno
Cornelis, Pierre
Zizi, Martin
Van Eldere, Johan
Deschaght, Pieter
Vaneechoutte, Mario
Jennes, Serge
Pitt, Tyrone
De Vos, Daniel
author_sort Pirnay, Jean-Paul
collection PubMed
description At present there are strong indications that Pseudomonas aeruginosa exhibits an epidemic population structure; clinical isolates are indistinguishable from environmental isolates, and they do not exhibit a specific (disease) habitat selection. However, some important issues, such as the worldwide emergence of highly transmissible P. aeruginosa clones among cystic fibrosis (CF) patients and the spread and persistence of multidrug resistant (MDR) strains in hospital wards with high antibiotic pressure, remain contentious. To further investigate the population structure of P. aeruginosa, eight parameters were analyzed and combined for 328 unrelated isolates, collected over the last 125 years from 69 localities in 30 countries on five continents, from diverse clinical (human and animal) and environmental habitats. The analysed parameters were: i) O serotype, ii) Fluorescent Amplified-Fragment Length Polymorphism (FALFP) pattern, nucleotide sequences of outer membrane protein genes, iii) oprI, iv) oprL, v) oprD, vi) pyoverdine receptor gene profile (fpvA type and fpvB prevalence), and prevalence of vii) exoenzyme genes exoS and exoU and viii) group I pilin glycosyltransferase gene tfpO. These traits were combined and analysed using biological data analysis software and visualized in the form of a minimum spanning tree (MST). We revealed a network of relationships between all analyzed parameters and non-congruence between experiments. At the same time we observed several conserved clones, characterized by an almost identical data set. These observations confirm the nonclonal epidemic population structure of P. aeruginosa, a superficially clonal structure with frequent recombinations, in which occasionally highly successful epidemic clones arise. One of these clones is the renown and widespread MDR serotype O12 clone. On the other hand, we found no evidence for a widespread CF transmissible clone. All but one of the 43 analysed CF strains belonged to a ubiquitous P. aeruginosa “core lineage” and typically exhibited the exoS (+)/exoU (−) genotype and group B oprL and oprD alleles. This is to our knowledge the first report of an MST analysis conducted on a polyphasic data set.
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spelling pubmed-27774102009-11-23 Pseudomonas aeruginosa Population Structure Revisited Pirnay, Jean-Paul Bilocq, Florence Pot, Bruno Cornelis, Pierre Zizi, Martin Van Eldere, Johan Deschaght, Pieter Vaneechoutte, Mario Jennes, Serge Pitt, Tyrone De Vos, Daniel PLoS One Research Article At present there are strong indications that Pseudomonas aeruginosa exhibits an epidemic population structure; clinical isolates are indistinguishable from environmental isolates, and they do not exhibit a specific (disease) habitat selection. However, some important issues, such as the worldwide emergence of highly transmissible P. aeruginosa clones among cystic fibrosis (CF) patients and the spread and persistence of multidrug resistant (MDR) strains in hospital wards with high antibiotic pressure, remain contentious. To further investigate the population structure of P. aeruginosa, eight parameters were analyzed and combined for 328 unrelated isolates, collected over the last 125 years from 69 localities in 30 countries on five continents, from diverse clinical (human and animal) and environmental habitats. The analysed parameters were: i) O serotype, ii) Fluorescent Amplified-Fragment Length Polymorphism (FALFP) pattern, nucleotide sequences of outer membrane protein genes, iii) oprI, iv) oprL, v) oprD, vi) pyoverdine receptor gene profile (fpvA type and fpvB prevalence), and prevalence of vii) exoenzyme genes exoS and exoU and viii) group I pilin glycosyltransferase gene tfpO. These traits were combined and analysed using biological data analysis software and visualized in the form of a minimum spanning tree (MST). We revealed a network of relationships between all analyzed parameters and non-congruence between experiments. At the same time we observed several conserved clones, characterized by an almost identical data set. These observations confirm the nonclonal epidemic population structure of P. aeruginosa, a superficially clonal structure with frequent recombinations, in which occasionally highly successful epidemic clones arise. One of these clones is the renown and widespread MDR serotype O12 clone. On the other hand, we found no evidence for a widespread CF transmissible clone. All but one of the 43 analysed CF strains belonged to a ubiquitous P. aeruginosa “core lineage” and typically exhibited the exoS (+)/exoU (−) genotype and group B oprL and oprD alleles. This is to our knowledge the first report of an MST analysis conducted on a polyphasic data set. Public Library of Science 2009-11-13 /pmc/articles/PMC2777410/ /pubmed/19936230 http://dx.doi.org/10.1371/journal.pone.0007740 Text en Pirnay et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Pirnay, Jean-Paul
Bilocq, Florence
Pot, Bruno
Cornelis, Pierre
Zizi, Martin
Van Eldere, Johan
Deschaght, Pieter
Vaneechoutte, Mario
Jennes, Serge
Pitt, Tyrone
De Vos, Daniel
Pseudomonas aeruginosa Population Structure Revisited
title Pseudomonas aeruginosa Population Structure Revisited
title_full Pseudomonas aeruginosa Population Structure Revisited
title_fullStr Pseudomonas aeruginosa Population Structure Revisited
title_full_unstemmed Pseudomonas aeruginosa Population Structure Revisited
title_short Pseudomonas aeruginosa Population Structure Revisited
title_sort pseudomonas aeruginosa population structure revisited
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2777410/
https://www.ncbi.nlm.nih.gov/pubmed/19936230
http://dx.doi.org/10.1371/journal.pone.0007740
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