Cargando…

Pseudomonas aeruginosa core metabolism exerts a widespread growth-independent control on virulence

To assess the role of core metabolism genes in bacterial virulence - independently of their effect on growth - we correlated the genome, the transcriptome and the pathogenicity in flies and mice of 30 fully sequenced Pseudomonas strains. Gene presence correlates robustly with pathogenicity differenc...

Descripción completa

Detalles Bibliográficos
Autores principales: Panayidou, Stavria, Georgiades, Kaliopi, Christofi, Theodoulakis, Tamana, Stella, Promponas, Vasilis J., Apidianakis, Yiorgos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7289854/
https://www.ncbi.nlm.nih.gov/pubmed/32528034
http://dx.doi.org/10.1038/s41598-020-66194-4
_version_ 1783545545660301312
author Panayidou, Stavria
Georgiades, Kaliopi
Christofi, Theodoulakis
Tamana, Stella
Promponas, Vasilis J.
Apidianakis, Yiorgos
author_facet Panayidou, Stavria
Georgiades, Kaliopi
Christofi, Theodoulakis
Tamana, Stella
Promponas, Vasilis J.
Apidianakis, Yiorgos
author_sort Panayidou, Stavria
collection PubMed
description To assess the role of core metabolism genes in bacterial virulence - independently of their effect on growth - we correlated the genome, the transcriptome and the pathogenicity in flies and mice of 30 fully sequenced Pseudomonas strains. Gene presence correlates robustly with pathogenicity differences among all Pseudomonas species, but not among the P. aeruginosa strains. However, gene expression differences are evident between highly and lowly pathogenic P. aeruginosa strains in multiple virulence factors and a few metabolism genes. Moreover, 16.5%, a noticeable fraction of the core metabolism genes of P. aeruginosa strain PA14 (compared to 8.5% of the non-metabolic genes tested), appear necessary for full virulence when mutated. Most of these virulence-defective core metabolism mutants are compromised in at least one key virulence mechanism independently of auxotrophy. A pathway level analysis of PA14 core metabolism, uncovers beta-oxidation and the biosynthesis of amino-acids, succinate, citramalate, and chorismate to be important for full virulence. Strikingly, the relative expression among P. aeruginosa strains of genes belonging in these metabolic pathways is indicative of their pathogenicity. Thus, P. aeruginosa strain-to-strain virulence variation, remains largely obscure at the genome level, but can be dissected at the pathway level via functional transcriptomics of core metabolism.
format Online
Article
Text
id pubmed-7289854
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-72898542020-06-15 Pseudomonas aeruginosa core metabolism exerts a widespread growth-independent control on virulence Panayidou, Stavria Georgiades, Kaliopi Christofi, Theodoulakis Tamana, Stella Promponas, Vasilis J. Apidianakis, Yiorgos Sci Rep Article To assess the role of core metabolism genes in bacterial virulence - independently of their effect on growth - we correlated the genome, the transcriptome and the pathogenicity in flies and mice of 30 fully sequenced Pseudomonas strains. Gene presence correlates robustly with pathogenicity differences among all Pseudomonas species, but not among the P. aeruginosa strains. However, gene expression differences are evident between highly and lowly pathogenic P. aeruginosa strains in multiple virulence factors and a few metabolism genes. Moreover, 16.5%, a noticeable fraction of the core metabolism genes of P. aeruginosa strain PA14 (compared to 8.5% of the non-metabolic genes tested), appear necessary for full virulence when mutated. Most of these virulence-defective core metabolism mutants are compromised in at least one key virulence mechanism independently of auxotrophy. A pathway level analysis of PA14 core metabolism, uncovers beta-oxidation and the biosynthesis of amino-acids, succinate, citramalate, and chorismate to be important for full virulence. Strikingly, the relative expression among P. aeruginosa strains of genes belonging in these metabolic pathways is indicative of their pathogenicity. Thus, P. aeruginosa strain-to-strain virulence variation, remains largely obscure at the genome level, but can be dissected at the pathway level via functional transcriptomics of core metabolism. Nature Publishing Group UK 2020-06-11 /pmc/articles/PMC7289854/ /pubmed/32528034 http://dx.doi.org/10.1038/s41598-020-66194-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Panayidou, Stavria
Georgiades, Kaliopi
Christofi, Theodoulakis
Tamana, Stella
Promponas, Vasilis J.
Apidianakis, Yiorgos
Pseudomonas aeruginosa core metabolism exerts a widespread growth-independent control on virulence
title Pseudomonas aeruginosa core metabolism exerts a widespread growth-independent control on virulence
title_full Pseudomonas aeruginosa core metabolism exerts a widespread growth-independent control on virulence
title_fullStr Pseudomonas aeruginosa core metabolism exerts a widespread growth-independent control on virulence
title_full_unstemmed Pseudomonas aeruginosa core metabolism exerts a widespread growth-independent control on virulence
title_short Pseudomonas aeruginosa core metabolism exerts a widespread growth-independent control on virulence
title_sort pseudomonas aeruginosa core metabolism exerts a widespread growth-independent control on virulence
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7289854/
https://www.ncbi.nlm.nih.gov/pubmed/32528034
http://dx.doi.org/10.1038/s41598-020-66194-4
work_keys_str_mv AT panayidoustavria pseudomonasaeruginosacoremetabolismexertsawidespreadgrowthindependentcontrolonvirulence
AT georgiadeskaliopi pseudomonasaeruginosacoremetabolismexertsawidespreadgrowthindependentcontrolonvirulence
AT christofitheodoulakis pseudomonasaeruginosacoremetabolismexertsawidespreadgrowthindependentcontrolonvirulence
AT tamanastella pseudomonasaeruginosacoremetabolismexertsawidespreadgrowthindependentcontrolonvirulence
AT promponasvasilisj pseudomonasaeruginosacoremetabolismexertsawidespreadgrowthindependentcontrolonvirulence
AT apidianakisyiorgos pseudomonasaeruginosacoremetabolismexertsawidespreadgrowthindependentcontrolonvirulence