Cargando…
Genomic characterization of the antiviral arsenal of Actinobacteria
Phages are ubiquitous in nature, and bacteria with very different genomics, metabolisms, and lifestyles are subjected to their predation. Yet, the defence systems that allow bacteria to resist their phages have rarely been explored experimentally outside a very limited number of model organisms. Act...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Microbiology Society
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10482375/ https://www.ncbi.nlm.nih.gov/pubmed/37531269 http://dx.doi.org/10.1099/mic.0.001374 |
_version_ | 1785102160128638976 |
---|---|
author | Georjon, Héloïse Tesson, Florian Shomar, Helena Bernheim, Aude |
author_facet | Georjon, Héloïse Tesson, Florian Shomar, Helena Bernheim, Aude |
author_sort | Georjon, Héloïse |
collection | PubMed |
description | Phages are ubiquitous in nature, and bacteria with very different genomics, metabolisms, and lifestyles are subjected to their predation. Yet, the defence systems that allow bacteria to resist their phages have rarely been explored experimentally outside a very limited number of model organisms. Actinobacteria (Actinomycetota) are a phylum of GC-rich Gram-positive bacteria, which often produce an important diversity of secondary metabolites. Despite being ubiquitous in a wide range of environments, from soil to fresh and sea water but also the gut microbiome, relatively little is known about the anti-phage arsenal of Actinobacteria. In this work, we used DefenseFinder to systematically detect 131 anti-phage defence systems in 22803 fully sequenced prokaryotic genomes, among which are 2253 Actinobacteria of more than 700 species. We show that, like other bacteria, Actinobacteria encode many diverse anti-phage systems that are often encoded on mobile genetic elements. We further demonstrate that most detected defence systems are absent or rarer in Actinobacteria than in other bacteria, while a few rare systems are enriched (notably gp29-gp30 and Wadjet). We characterize the spatial distribution of anti-phage systems on Streptomyces chromosomes and show that some defence systems (e.g. RM systems) tend to be encoded in the core region, while others (e.g. Lamassu and Wadjet) are enriched towards the extremities. Overall, our results suggest that Actinobacteria might be a source of novel anti-phage systems and provide clues to characterize mechanistic aspects of known anti-phage systems. |
format | Online Article Text |
id | pubmed-10482375 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Microbiology Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-104823752023-09-07 Genomic characterization of the antiviral arsenal of Actinobacteria Georjon, Héloïse Tesson, Florian Shomar, Helena Bernheim, Aude Microbiology (Reading) Microbial Evolution Phages are ubiquitous in nature, and bacteria with very different genomics, metabolisms, and lifestyles are subjected to their predation. Yet, the defence systems that allow bacteria to resist their phages have rarely been explored experimentally outside a very limited number of model organisms. Actinobacteria (Actinomycetota) are a phylum of GC-rich Gram-positive bacteria, which often produce an important diversity of secondary metabolites. Despite being ubiquitous in a wide range of environments, from soil to fresh and sea water but also the gut microbiome, relatively little is known about the anti-phage arsenal of Actinobacteria. In this work, we used DefenseFinder to systematically detect 131 anti-phage defence systems in 22803 fully sequenced prokaryotic genomes, among which are 2253 Actinobacteria of more than 700 species. We show that, like other bacteria, Actinobacteria encode many diverse anti-phage systems that are often encoded on mobile genetic elements. We further demonstrate that most detected defence systems are absent or rarer in Actinobacteria than in other bacteria, while a few rare systems are enriched (notably gp29-gp30 and Wadjet). We characterize the spatial distribution of anti-phage systems on Streptomyces chromosomes and show that some defence systems (e.g. RM systems) tend to be encoded in the core region, while others (e.g. Lamassu and Wadjet) are enriched towards the extremities. Overall, our results suggest that Actinobacteria might be a source of novel anti-phage systems and provide clues to characterize mechanistic aspects of known anti-phage systems. Microbiology Society 2023-08-02 /pmc/articles/PMC10482375/ /pubmed/37531269 http://dx.doi.org/10.1099/mic.0.001374 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License. The Microbiology Society waived the open access fees for this article. |
spellingShingle | Microbial Evolution Georjon, Héloïse Tesson, Florian Shomar, Helena Bernheim, Aude Genomic characterization of the antiviral arsenal of Actinobacteria |
title | Genomic characterization of the antiviral arsenal of Actinobacteria |
title_full | Genomic characterization of the antiviral arsenal of Actinobacteria |
title_fullStr | Genomic characterization of the antiviral arsenal of Actinobacteria |
title_full_unstemmed | Genomic characterization of the antiviral arsenal of Actinobacteria |
title_short | Genomic characterization of the antiviral arsenal of Actinobacteria |
title_sort | genomic characterization of the antiviral arsenal of actinobacteria |
topic | Microbial Evolution |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10482375/ https://www.ncbi.nlm.nih.gov/pubmed/37531269 http://dx.doi.org/10.1099/mic.0.001374 |
work_keys_str_mv | AT georjonheloise genomiccharacterizationoftheantiviralarsenalofactinobacteria AT tessonflorian genomiccharacterizationoftheantiviralarsenalofactinobacteria AT shomarhelena genomiccharacterizationoftheantiviralarsenalofactinobacteria AT bernheimaude genomiccharacterizationoftheantiviralarsenalofactinobacteria |