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The Pseudomonas aeruginosa accessory genome elements influence virulence towards Caenorhabditis elegans
BACKGROUND: Multicellular animals and bacteria frequently engage in predator-prey and host-pathogen interactions, such as the well-studied relationship between Pseudomonas aeruginosa and the nematode Caenorhabditis elegans. This study investigates the genomic and genetic basis of bacterial-driven va...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6902481/ https://www.ncbi.nlm.nih.gov/pubmed/31823826 http://dx.doi.org/10.1186/s13059-019-1890-1 |
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author | Vasquez-Rifo, Alejandro Veksler-Lublinsky, Isana Cheng, Zhenyu Ausubel, Frederick M. Ambros, Victor |
author_facet | Vasquez-Rifo, Alejandro Veksler-Lublinsky, Isana Cheng, Zhenyu Ausubel, Frederick M. Ambros, Victor |
author_sort | Vasquez-Rifo, Alejandro |
collection | PubMed |
description | BACKGROUND: Multicellular animals and bacteria frequently engage in predator-prey and host-pathogen interactions, such as the well-studied relationship between Pseudomonas aeruginosa and the nematode Caenorhabditis elegans. This study investigates the genomic and genetic basis of bacterial-driven variability in P. aeruginosa virulence towards C. elegans to provide evolutionary insights into host-pathogen relationships. RESULTS: Natural isolates of P. aeruginosa that exhibit diverse genomes display a broad range of virulence towards C. elegans. Using gene association and genetic analysis, we identify accessory genome elements that correlate with virulence, including both known and novel virulence determinants. Among the novel genes, we find a viral-like mobile element, the teg block, that impairs virulence and whose acquisition is restricted by CRISPR-Cas systems. Further genetic and genomic evidence suggests that spacer-targeted elements preferentially associate with lower virulence while the presence of CRISPR-Cas associates with higher virulence. CONCLUSIONS: Our analysis demonstrates substantial strain variation in P. aeruginosa virulence, mediated by specific accessory genome elements that promote increased or decreased virulence. We exemplify that viral-like accessory genome elements that decrease virulence can be restricted by bacterial CRISPR-Cas immune defense systems, and suggest a positive, albeit indirect, role for host CRISPR-Cas systems in virulence maintenance. |
format | Online Article Text |
id | pubmed-6902481 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-69024812019-12-11 The Pseudomonas aeruginosa accessory genome elements influence virulence towards Caenorhabditis elegans Vasquez-Rifo, Alejandro Veksler-Lublinsky, Isana Cheng, Zhenyu Ausubel, Frederick M. Ambros, Victor Genome Biol Research BACKGROUND: Multicellular animals and bacteria frequently engage in predator-prey and host-pathogen interactions, such as the well-studied relationship between Pseudomonas aeruginosa and the nematode Caenorhabditis elegans. This study investigates the genomic and genetic basis of bacterial-driven variability in P. aeruginosa virulence towards C. elegans to provide evolutionary insights into host-pathogen relationships. RESULTS: Natural isolates of P. aeruginosa that exhibit diverse genomes display a broad range of virulence towards C. elegans. Using gene association and genetic analysis, we identify accessory genome elements that correlate with virulence, including both known and novel virulence determinants. Among the novel genes, we find a viral-like mobile element, the teg block, that impairs virulence and whose acquisition is restricted by CRISPR-Cas systems. Further genetic and genomic evidence suggests that spacer-targeted elements preferentially associate with lower virulence while the presence of CRISPR-Cas associates with higher virulence. CONCLUSIONS: Our analysis demonstrates substantial strain variation in P. aeruginosa virulence, mediated by specific accessory genome elements that promote increased or decreased virulence. We exemplify that viral-like accessory genome elements that decrease virulence can be restricted by bacterial CRISPR-Cas immune defense systems, and suggest a positive, albeit indirect, role for host CRISPR-Cas systems in virulence maintenance. BioMed Central 2019-12-10 /pmc/articles/PMC6902481/ /pubmed/31823826 http://dx.doi.org/10.1186/s13059-019-1890-1 Text en © The Author(s). 2019 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 Vasquez-Rifo, Alejandro Veksler-Lublinsky, Isana Cheng, Zhenyu Ausubel, Frederick M. Ambros, Victor The Pseudomonas aeruginosa accessory genome elements influence virulence towards Caenorhabditis elegans |
title | The Pseudomonas aeruginosa accessory genome elements influence virulence towards Caenorhabditis elegans |
title_full | The Pseudomonas aeruginosa accessory genome elements influence virulence towards Caenorhabditis elegans |
title_fullStr | The Pseudomonas aeruginosa accessory genome elements influence virulence towards Caenorhabditis elegans |
title_full_unstemmed | The Pseudomonas aeruginosa accessory genome elements influence virulence towards Caenorhabditis elegans |
title_short | The Pseudomonas aeruginosa accessory genome elements influence virulence towards Caenorhabditis elegans |
title_sort | pseudomonas aeruginosa accessory genome elements influence virulence towards caenorhabditis elegans |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6902481/ https://www.ncbi.nlm.nih.gov/pubmed/31823826 http://dx.doi.org/10.1186/s13059-019-1890-1 |
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