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Comparative genomics and biological characterization of sequential Pseudomonas aeruginosa isolates from persistent airways infection

BACKGROUND: Pseudomonas aeruginosa establishes life-long chronic airway infections in cystic fibrosis (CF) patients. As the disease progresses, P. aeruginosa pathoadaptive variants are distinguished from the initially acquired strain. However, the genetic basis and the biology of host-bacteria inter...

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Autores principales: Bianconi, Irene, Jeukens, Julie, Freschi, Luca, Alcalá-Franco, Beatriz, Facchini, Marcella, Boyle, Brian, Molinaro, Antonio, Kukavica-Ibrulj, Irena, Tümmler, Burkhard, Levesque, Roger C., Bragonzi, Alessandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4696338/
https://www.ncbi.nlm.nih.gov/pubmed/26714629
http://dx.doi.org/10.1186/s12864-015-2276-8
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author Bianconi, Irene
Jeukens, Julie
Freschi, Luca
Alcalá-Franco, Beatriz
Facchini, Marcella
Boyle, Brian
Molinaro, Antonio
Kukavica-Ibrulj, Irena
Tümmler, Burkhard
Levesque, Roger C.
Bragonzi, Alessandra
author_facet Bianconi, Irene
Jeukens, Julie
Freschi, Luca
Alcalá-Franco, Beatriz
Facchini, Marcella
Boyle, Brian
Molinaro, Antonio
Kukavica-Ibrulj, Irena
Tümmler, Burkhard
Levesque, Roger C.
Bragonzi, Alessandra
author_sort Bianconi, Irene
collection PubMed
description BACKGROUND: Pseudomonas aeruginosa establishes life-long chronic airway infections in cystic fibrosis (CF) patients. As the disease progresses, P. aeruginosa pathoadaptive variants are distinguished from the initially acquired strain. However, the genetic basis and the biology of host-bacteria interactions leading to a persistent lifestyle of P. aeruginosa are not understood. As a model system to study long term and persistent CF infections, the P. aeruginosa RP73, isolated 16.9 years after the onset of airways colonization from a CF patient, was investigated. Comparisons with strains RP1, isolated at the onset of the colonization, and clonal RP45, isolated 7 years before RP73 were carried out to better characterize genomic evolution of P. aeruginosa in the context of CF pathogenicity. RESULTS: Virulence assessments in disease animal model, genome sequencing and comparative genomics analysis were performed for clinical RP73, RP45, RP1 and prototype strains. In murine model, RP73 showed lower lethality and a remarkable capability of long-term persistence in chronic airways infection when compared to other strains. Pathological analysis of murine lungs confirmed advanced chronic pulmonary disease, inflammation and mucus secretory cells hyperplasia. Genomic analysis predicted twelve genomic islands in the RP73 genome, some of which distinguished RP73 from other prototype strains and corresponded to regions of genome plasticity. Further, comparative genomic analyses with sequential RP isolates showed signatures of pathoadaptive mutations in virulence factors potentially linked to the development of chronic infections in CF. CONCLUSIONS: The genome plasticity of P. aeruginosa particularly in the RP73 strain strongly indicated that these alterations may form the genetic basis defining host-bacteria interactions leading to a persistent lifestyle in human lungs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-2276-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-46963382015-12-31 Comparative genomics and biological characterization of sequential Pseudomonas aeruginosa isolates from persistent airways infection Bianconi, Irene Jeukens, Julie Freschi, Luca Alcalá-Franco, Beatriz Facchini, Marcella Boyle, Brian Molinaro, Antonio Kukavica-Ibrulj, Irena Tümmler, Burkhard Levesque, Roger C. Bragonzi, Alessandra BMC Genomics Research Article BACKGROUND: Pseudomonas aeruginosa establishes life-long chronic airway infections in cystic fibrosis (CF) patients. As the disease progresses, P. aeruginosa pathoadaptive variants are distinguished from the initially acquired strain. However, the genetic basis and the biology of host-bacteria interactions leading to a persistent lifestyle of P. aeruginosa are not understood. As a model system to study long term and persistent CF infections, the P. aeruginosa RP73, isolated 16.9 years after the onset of airways colonization from a CF patient, was investigated. Comparisons with strains RP1, isolated at the onset of the colonization, and clonal RP45, isolated 7 years before RP73 were carried out to better characterize genomic evolution of P. aeruginosa in the context of CF pathogenicity. RESULTS: Virulence assessments in disease animal model, genome sequencing and comparative genomics analysis were performed for clinical RP73, RP45, RP1 and prototype strains. In murine model, RP73 showed lower lethality and a remarkable capability of long-term persistence in chronic airways infection when compared to other strains. Pathological analysis of murine lungs confirmed advanced chronic pulmonary disease, inflammation and mucus secretory cells hyperplasia. Genomic analysis predicted twelve genomic islands in the RP73 genome, some of which distinguished RP73 from other prototype strains and corresponded to regions of genome plasticity. Further, comparative genomic analyses with sequential RP isolates showed signatures of pathoadaptive mutations in virulence factors potentially linked to the development of chronic infections in CF. CONCLUSIONS: The genome plasticity of P. aeruginosa particularly in the RP73 strain strongly indicated that these alterations may form the genetic basis defining host-bacteria interactions leading to a persistent lifestyle in human lungs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-2276-8) contains supplementary material, which is available to authorized users. BioMed Central 2015-12-29 /pmc/articles/PMC4696338/ /pubmed/26714629 http://dx.doi.org/10.1186/s12864-015-2276-8 Text en © Bianconi et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Bianconi, Irene
Jeukens, Julie
Freschi, Luca
Alcalá-Franco, Beatriz
Facchini, Marcella
Boyle, Brian
Molinaro, Antonio
Kukavica-Ibrulj, Irena
Tümmler, Burkhard
Levesque, Roger C.
Bragonzi, Alessandra
Comparative genomics and biological characterization of sequential Pseudomonas aeruginosa isolates from persistent airways infection
title Comparative genomics and biological characterization of sequential Pseudomonas aeruginosa isolates from persistent airways infection
title_full Comparative genomics and biological characterization of sequential Pseudomonas aeruginosa isolates from persistent airways infection
title_fullStr Comparative genomics and biological characterization of sequential Pseudomonas aeruginosa isolates from persistent airways infection
title_full_unstemmed Comparative genomics and biological characterization of sequential Pseudomonas aeruginosa isolates from persistent airways infection
title_short Comparative genomics and biological characterization of sequential Pseudomonas aeruginosa isolates from persistent airways infection
title_sort comparative genomics and biological characterization of sequential pseudomonas aeruginosa isolates from persistent airways infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4696338/
https://www.ncbi.nlm.nih.gov/pubmed/26714629
http://dx.doi.org/10.1186/s12864-015-2276-8
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