Cargando…

Genomic analysis reveals that Pseudomonas aeruginosa virulence is combinatorial

BACKGROUND: Pseudomonas aeruginosa is a ubiquitous environmental bacterium and an important opportunistic human pathogen. Generally, the acquisition of genes in the form of pathogenicity islands distinguishes pathogenic isolates from nonpathogens. We therefore sequenced a highly virulent strain of P...

Descripción completa

Detalles Bibliográficos
Autores principales: Lee, Daniel G, Urbach, Jonathan M, Wu, Gang, Liberati, Nicole T, Feinbaum, Rhonda L, Miyata, Sachiko, Diggins, Lenard T, He, Jianxin, Saucier, Maude, Déziel, Eric, Friedman, Lisa, Li, Li, Grills, George, Montgomery, Kate, Kucherlapati, Raju, Rahme, Laurence G, Ausubel, Frederick M
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1794565/
https://www.ncbi.nlm.nih.gov/pubmed/17038190
http://dx.doi.org/10.1186/gb-2006-7-10-r90
_version_ 1782132212524646400
author Lee, Daniel G
Urbach, Jonathan M
Wu, Gang
Liberati, Nicole T
Feinbaum, Rhonda L
Miyata, Sachiko
Diggins, Lenard T
He, Jianxin
Saucier, Maude
Déziel, Eric
Friedman, Lisa
Li, Li
Grills, George
Montgomery, Kate
Kucherlapati, Raju
Rahme, Laurence G
Ausubel, Frederick M
author_facet Lee, Daniel G
Urbach, Jonathan M
Wu, Gang
Liberati, Nicole T
Feinbaum, Rhonda L
Miyata, Sachiko
Diggins, Lenard T
He, Jianxin
Saucier, Maude
Déziel, Eric
Friedman, Lisa
Li, Li
Grills, George
Montgomery, Kate
Kucherlapati, Raju
Rahme, Laurence G
Ausubel, Frederick M
author_sort Lee, Daniel G
collection PubMed
description BACKGROUND: Pseudomonas aeruginosa is a ubiquitous environmental bacterium and an important opportunistic human pathogen. Generally, the acquisition of genes in the form of pathogenicity islands distinguishes pathogenic isolates from nonpathogens. We therefore sequenced a highly virulent strain of P. aeruginosa, PA14, and compared it with a previously sequenced (and less pathogenic) strain, PAO1, to identify novel virulence genes. RESULTS: The PA14 and PAO1 genomes are remarkably similar, although PA14 has a slightly larger genome (6.5 megabses [Mb]) than does PAO1 (6.3 Mb). We identified 58 PA14 gene clusters that are absent in PAO1 to determine which of these genes, if any, contribute to its enhanced virulence in a Caenorhabditis elegans pathogenicity model. First, we tested 18 additional diverse strains in the C. elegans model and observed a wide range of pathogenic potential; however, genotyping these strains using a custom microarray showed that the presence of PA14 genes that are absent in PAO1 did not correlate with the virulence of these strains. Second, we utilized a full-genome nonredundant mutant library of PA14 to identify five genes (absent in PAO1) required for C. elegans killing. Surprisingly, although these five genes are present in many other P. aeruginosa strains, they do not correlate with virulence in C. elegans. CONCLUSION: Genes required for pathogenicity in one strain of P. aeruginosa are neither required for nor predictive of virulence in other strains. We therefore propose that virulence in this organism is both multifactorial and combinatorial, the result of a pool of pathogenicity-related genes that interact in various combinations in different genetic backgrounds.
format Text
id pubmed-1794565
institution National Center for Biotechnology Information
language English
publishDate 2006
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-17945652007-02-08 Genomic analysis reveals that Pseudomonas aeruginosa virulence is combinatorial Lee, Daniel G Urbach, Jonathan M Wu, Gang Liberati, Nicole T Feinbaum, Rhonda L Miyata, Sachiko Diggins, Lenard T He, Jianxin Saucier, Maude Déziel, Eric Friedman, Lisa Li, Li Grills, George Montgomery, Kate Kucherlapati, Raju Rahme, Laurence G Ausubel, Frederick M Genome Biol Research BACKGROUND: Pseudomonas aeruginosa is a ubiquitous environmental bacterium and an important opportunistic human pathogen. Generally, the acquisition of genes in the form of pathogenicity islands distinguishes pathogenic isolates from nonpathogens. We therefore sequenced a highly virulent strain of P. aeruginosa, PA14, and compared it with a previously sequenced (and less pathogenic) strain, PAO1, to identify novel virulence genes. RESULTS: The PA14 and PAO1 genomes are remarkably similar, although PA14 has a slightly larger genome (6.5 megabses [Mb]) than does PAO1 (6.3 Mb). We identified 58 PA14 gene clusters that are absent in PAO1 to determine which of these genes, if any, contribute to its enhanced virulence in a Caenorhabditis elegans pathogenicity model. First, we tested 18 additional diverse strains in the C. elegans model and observed a wide range of pathogenic potential; however, genotyping these strains using a custom microarray showed that the presence of PA14 genes that are absent in PAO1 did not correlate with the virulence of these strains. Second, we utilized a full-genome nonredundant mutant library of PA14 to identify five genes (absent in PAO1) required for C. elegans killing. Surprisingly, although these five genes are present in many other P. aeruginosa strains, they do not correlate with virulence in C. elegans. CONCLUSION: Genes required for pathogenicity in one strain of P. aeruginosa are neither required for nor predictive of virulence in other strains. We therefore propose that virulence in this organism is both multifactorial and combinatorial, the result of a pool of pathogenicity-related genes that interact in various combinations in different genetic backgrounds. BioMed Central 2006 2006-10-12 /pmc/articles/PMC1794565/ /pubmed/17038190 http://dx.doi.org/10.1186/gb-2006-7-10-r90 Text en Copyright © 2006 Lee et al.; licensee BioMed Central Ltd http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Lee, Daniel G
Urbach, Jonathan M
Wu, Gang
Liberati, Nicole T
Feinbaum, Rhonda L
Miyata, Sachiko
Diggins, Lenard T
He, Jianxin
Saucier, Maude
Déziel, Eric
Friedman, Lisa
Li, Li
Grills, George
Montgomery, Kate
Kucherlapati, Raju
Rahme, Laurence G
Ausubel, Frederick M
Genomic analysis reveals that Pseudomonas aeruginosa virulence is combinatorial
title Genomic analysis reveals that Pseudomonas aeruginosa virulence is combinatorial
title_full Genomic analysis reveals that Pseudomonas aeruginosa virulence is combinatorial
title_fullStr Genomic analysis reveals that Pseudomonas aeruginosa virulence is combinatorial
title_full_unstemmed Genomic analysis reveals that Pseudomonas aeruginosa virulence is combinatorial
title_short Genomic analysis reveals that Pseudomonas aeruginosa virulence is combinatorial
title_sort genomic analysis reveals that pseudomonas aeruginosa virulence is combinatorial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1794565/
https://www.ncbi.nlm.nih.gov/pubmed/17038190
http://dx.doi.org/10.1186/gb-2006-7-10-r90
work_keys_str_mv AT leedanielg genomicanalysisrevealsthatpseudomonasaeruginosavirulenceiscombinatorial
AT urbachjonathanm genomicanalysisrevealsthatpseudomonasaeruginosavirulenceiscombinatorial
AT wugang genomicanalysisrevealsthatpseudomonasaeruginosavirulenceiscombinatorial
AT liberatinicolet genomicanalysisrevealsthatpseudomonasaeruginosavirulenceiscombinatorial
AT feinbaumrhondal genomicanalysisrevealsthatpseudomonasaeruginosavirulenceiscombinatorial
AT miyatasachiko genomicanalysisrevealsthatpseudomonasaeruginosavirulenceiscombinatorial
AT digginslenardt genomicanalysisrevealsthatpseudomonasaeruginosavirulenceiscombinatorial
AT hejianxin genomicanalysisrevealsthatpseudomonasaeruginosavirulenceiscombinatorial
AT sauciermaude genomicanalysisrevealsthatpseudomonasaeruginosavirulenceiscombinatorial
AT dezieleric genomicanalysisrevealsthatpseudomonasaeruginosavirulenceiscombinatorial
AT friedmanlisa genomicanalysisrevealsthatpseudomonasaeruginosavirulenceiscombinatorial
AT lili genomicanalysisrevealsthatpseudomonasaeruginosavirulenceiscombinatorial
AT grillsgeorge genomicanalysisrevealsthatpseudomonasaeruginosavirulenceiscombinatorial
AT montgomerykate genomicanalysisrevealsthatpseudomonasaeruginosavirulenceiscombinatorial
AT kucherlapatiraju genomicanalysisrevealsthatpseudomonasaeruginosavirulenceiscombinatorial
AT rahmelaurenceg genomicanalysisrevealsthatpseudomonasaeruginosavirulenceiscombinatorial
AT ausubelfrederickm genomicanalysisrevealsthatpseudomonasaeruginosavirulenceiscombinatorial