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Simultaneous entry as an adaptation to virulence in a novel satellite-helper system infecting Streptomyces species

Satellites are mobile genetic elements that are dependent upon the replication machinery of their helper viruses. Bacteriophages have provided many examples of satellite nucleic acids that utilize their helper morphogenic genes for propagation. Here we describe two novel satellite-helper phage syste...

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Autores principales: deCarvalho, Tagide, Mascolo, Elia, Caruso, Steven M., López-Pérez, Júlia, Weston-Hafer, Kathleen, Shaffer, Christopher, Erill, Ivan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10690885/
https://www.ncbi.nlm.nih.gov/pubmed/37907733
http://dx.doi.org/10.1038/s41396-023-01548-0
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author deCarvalho, Tagide
Mascolo, Elia
Caruso, Steven M.
López-Pérez, Júlia
Weston-Hafer, Kathleen
Shaffer, Christopher
Erill, Ivan
author_facet deCarvalho, Tagide
Mascolo, Elia
Caruso, Steven M.
López-Pérez, Júlia
Weston-Hafer, Kathleen
Shaffer, Christopher
Erill, Ivan
author_sort deCarvalho, Tagide
collection PubMed
description Satellites are mobile genetic elements that are dependent upon the replication machinery of their helper viruses. Bacteriophages have provided many examples of satellite nucleic acids that utilize their helper morphogenic genes for propagation. Here we describe two novel satellite-helper phage systems, Mulch and Flayer, that infect Streptomyces species. The satellites in these systems encode for encapsidation machinery but have an absence of key replication genes, thus providing the first example of bacteriophage satellite viruses. We also show that codon usage of the satellites matches the tRNA gene content of the helpers. The satellite in one of these systems, Flayer, does not appear to integrate into the host genome, which represents the first example of a virulent satellite phage. The Flayer satellite has a unique tail adaptation that allows it to attach to its helper for simultaneous co-infection. These findings demonstrate an ever-increasing array of satellite strategies for genetic dependence on their helpers in the evolutionary arms race between satellite and helper phages. [Image: see text]
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spelling pubmed-106908852023-12-02 Simultaneous entry as an adaptation to virulence in a novel satellite-helper system infecting Streptomyces species deCarvalho, Tagide Mascolo, Elia Caruso, Steven M. López-Pérez, Júlia Weston-Hafer, Kathleen Shaffer, Christopher Erill, Ivan ISME J Article Satellites are mobile genetic elements that are dependent upon the replication machinery of their helper viruses. Bacteriophages have provided many examples of satellite nucleic acids that utilize their helper morphogenic genes for propagation. Here we describe two novel satellite-helper phage systems, Mulch and Flayer, that infect Streptomyces species. The satellites in these systems encode for encapsidation machinery but have an absence of key replication genes, thus providing the first example of bacteriophage satellite viruses. We also show that codon usage of the satellites matches the tRNA gene content of the helpers. The satellite in one of these systems, Flayer, does not appear to integrate into the host genome, which represents the first example of a virulent satellite phage. The Flayer satellite has a unique tail adaptation that allows it to attach to its helper for simultaneous co-infection. These findings demonstrate an ever-increasing array of satellite strategies for genetic dependence on their helpers in the evolutionary arms race between satellite and helper phages. [Image: see text] Nature Publishing Group UK 2023-10-31 2023-12 /pmc/articles/PMC10690885/ /pubmed/37907733 http://dx.doi.org/10.1038/s41396-023-01548-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 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/) .
spellingShingle Article
deCarvalho, Tagide
Mascolo, Elia
Caruso, Steven M.
López-Pérez, Júlia
Weston-Hafer, Kathleen
Shaffer, Christopher
Erill, Ivan
Simultaneous entry as an adaptation to virulence in a novel satellite-helper system infecting Streptomyces species
title Simultaneous entry as an adaptation to virulence in a novel satellite-helper system infecting Streptomyces species
title_full Simultaneous entry as an adaptation to virulence in a novel satellite-helper system infecting Streptomyces species
title_fullStr Simultaneous entry as an adaptation to virulence in a novel satellite-helper system infecting Streptomyces species
title_full_unstemmed Simultaneous entry as an adaptation to virulence in a novel satellite-helper system infecting Streptomyces species
title_short Simultaneous entry as an adaptation to virulence in a novel satellite-helper system infecting Streptomyces species
title_sort simultaneous entry as an adaptation to virulence in a novel satellite-helper system infecting streptomyces species
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10690885/
https://www.ncbi.nlm.nih.gov/pubmed/37907733
http://dx.doi.org/10.1038/s41396-023-01548-0
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