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Tyroviruses are a new group of temperate phages that infect Bacillus species in soil environments worldwide
BACKGROUND: Bacteriophages are widely considered to be highly abundant and genetically diverse, with their role in the evolution and virulence of many pathogens becoming increasingly clear. Less attention has been paid on phages preying on Bacillus, despite the potential for some of its members, suc...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9703825/ https://www.ncbi.nlm.nih.gov/pubmed/36443683 http://dx.doi.org/10.1186/s12864-022-09023-4 |
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author | Batinovic, Steven Stanton, Cassandra R. Rice, Daniel T. F. Rowe, Brittany Beer, Michael Petrovski, Steve |
author_facet | Batinovic, Steven Stanton, Cassandra R. Rice, Daniel T. F. Rowe, Brittany Beer, Michael Petrovski, Steve |
author_sort | Batinovic, Steven |
collection | PubMed |
description | BACKGROUND: Bacteriophages are widely considered to be highly abundant and genetically diverse, with their role in the evolution and virulence of many pathogens becoming increasingly clear. Less attention has been paid on phages preying on Bacillus, despite the potential for some of its members, such as Bacillus anthracis, to cause serious human disease. RESULTS: We have isolated five phages infecting the causative agent of anthrax, Bacillus anthracis. Using modern phylogenetic approaches we place these five new Bacillus phages, as well as 21 similar phage genomes retrieved from publicly available databases and metagenomic datasets into the Tyrovirus group, a newly proposed group named so due to the conservation of three distinct tyrosine recombinases. Genomic analysis of these large phages (~ 160–170 kb) reveals their DNA packaging mechanism and genomic features contributing to virion morphogenesis, host cell lysis and phage DNA replication processes. Analysis of the three tyrosine recombinases suggest Tyroviruses undergo a prophage lifecycle that may involve both host integration and plasmid stages. Further we show that Tyroviruses rely on divergent invasion mechanisms, with a subset requiring host S-layer for infection. CONCLUSIONS: Ultimately, we expand upon our understanding on the classification, phylogeny, and genomic organisation of a new and substantial phage group that prey on critically relevant Bacillus species. In an era characterised by a rapidly evolving landscape of phage genomics the deposition of future Tyroviruses will allow the further unravelling of the global spread and evolutionary history of these Bacillus phages. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-022-09023-4. |
format | Online Article Text |
id | pubmed-9703825 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-97038252022-11-29 Tyroviruses are a new group of temperate phages that infect Bacillus species in soil environments worldwide Batinovic, Steven Stanton, Cassandra R. Rice, Daniel T. F. Rowe, Brittany Beer, Michael Petrovski, Steve BMC Genomics Research BACKGROUND: Bacteriophages are widely considered to be highly abundant and genetically diverse, with their role in the evolution and virulence of many pathogens becoming increasingly clear. Less attention has been paid on phages preying on Bacillus, despite the potential for some of its members, such as Bacillus anthracis, to cause serious human disease. RESULTS: We have isolated five phages infecting the causative agent of anthrax, Bacillus anthracis. Using modern phylogenetic approaches we place these five new Bacillus phages, as well as 21 similar phage genomes retrieved from publicly available databases and metagenomic datasets into the Tyrovirus group, a newly proposed group named so due to the conservation of three distinct tyrosine recombinases. Genomic analysis of these large phages (~ 160–170 kb) reveals their DNA packaging mechanism and genomic features contributing to virion morphogenesis, host cell lysis and phage DNA replication processes. Analysis of the three tyrosine recombinases suggest Tyroviruses undergo a prophage lifecycle that may involve both host integration and plasmid stages. Further we show that Tyroviruses rely on divergent invasion mechanisms, with a subset requiring host S-layer for infection. CONCLUSIONS: Ultimately, we expand upon our understanding on the classification, phylogeny, and genomic organisation of a new and substantial phage group that prey on critically relevant Bacillus species. In an era characterised by a rapidly evolving landscape of phage genomics the deposition of future Tyroviruses will allow the further unravelling of the global spread and evolutionary history of these Bacillus phages. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-022-09023-4. BioMed Central 2022-11-28 /pmc/articles/PMC9703825/ /pubmed/36443683 http://dx.doi.org/10.1186/s12864-022-09023-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Batinovic, Steven Stanton, Cassandra R. Rice, Daniel T. F. Rowe, Brittany Beer, Michael Petrovski, Steve Tyroviruses are a new group of temperate phages that infect Bacillus species in soil environments worldwide |
title | Tyroviruses are a new group of temperate phages that infect Bacillus species in soil environments worldwide |
title_full | Tyroviruses are a new group of temperate phages that infect Bacillus species in soil environments worldwide |
title_fullStr | Tyroviruses are a new group of temperate phages that infect Bacillus species in soil environments worldwide |
title_full_unstemmed | Tyroviruses are a new group of temperate phages that infect Bacillus species in soil environments worldwide |
title_short | Tyroviruses are a new group of temperate phages that infect Bacillus species in soil environments worldwide |
title_sort | tyroviruses are a new group of temperate phages that infect bacillus species in soil environments worldwide |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9703825/ https://www.ncbi.nlm.nih.gov/pubmed/36443683 http://dx.doi.org/10.1186/s12864-022-09023-4 |
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