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Intraspecific antagonism through viral toxin encoded by chronic Sulfolobus spindle-shaped virus

Virus–host interactions evolve along a symbiosis continuum from antagonism to mutualism. Long-term associations between virus and host, such as those in chronic infection, will select for traits that drive the interaction towards mutualism, especially when susceptible hosts are rare in the populatio...

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Detalles Bibliográficos
Autores principales: DeWerff, Samantha J., Zhang, Changyi, Schneider, John, Whitaker, Rachel J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8628083/
https://www.ncbi.nlm.nih.gov/pubmed/34839697
http://dx.doi.org/10.1098/rstb.2020.0476
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author DeWerff, Samantha J.
Zhang, Changyi
Schneider, John
Whitaker, Rachel J.
author_facet DeWerff, Samantha J.
Zhang, Changyi
Schneider, John
Whitaker, Rachel J.
author_sort DeWerff, Samantha J.
collection PubMed
description Virus–host interactions evolve along a symbiosis continuum from antagonism to mutualism. Long-term associations between virus and host, such as those in chronic infection, will select for traits that drive the interaction towards mutualism, especially when susceptible hosts are rare in the population. Virus–host mutualism has been demonstrated in thermophilic archaeal populations where Sulfolobus spindle-shaped viruses (SSVs) provide a competitive advantage to their host Sulfolobus islandicus by producing a toxin that kills uninfected strains. Here, we determine the genetic basis of this killing phenotype by identifying highly transcribed genes in cells that are chronically infected with a diversity of SSVs. We demonstrate that these genes alone confer growth inhibition by being expressed in uninfected cells via a Sulfolobus expression plasmid. Challenge of chronically infected strains with vector-expressed toxins revealed a nested network of cross-toxicity among divergent SSVs, with both broad and specific toxin efficacies. This suggests that competition between viruses and/or their hosts could maintain toxin diversity. We propose that competitive interactions among chronic viruses to promote their host fitness form the basis of virus–host mutualism. This article is part of the theme issue ‘The secret lives of microbial mobile genetic elements’.
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spelling pubmed-86280832021-12-23 Intraspecific antagonism through viral toxin encoded by chronic Sulfolobus spindle-shaped virus DeWerff, Samantha J. Zhang, Changyi Schneider, John Whitaker, Rachel J. Philos Trans R Soc Lond B Biol Sci Articles Virus–host interactions evolve along a symbiosis continuum from antagonism to mutualism. Long-term associations between virus and host, such as those in chronic infection, will select for traits that drive the interaction towards mutualism, especially when susceptible hosts are rare in the population. Virus–host mutualism has been demonstrated in thermophilic archaeal populations where Sulfolobus spindle-shaped viruses (SSVs) provide a competitive advantage to their host Sulfolobus islandicus by producing a toxin that kills uninfected strains. Here, we determine the genetic basis of this killing phenotype by identifying highly transcribed genes in cells that are chronically infected with a diversity of SSVs. We demonstrate that these genes alone confer growth inhibition by being expressed in uninfected cells via a Sulfolobus expression plasmid. Challenge of chronically infected strains with vector-expressed toxins revealed a nested network of cross-toxicity among divergent SSVs, with both broad and specific toxin efficacies. This suggests that competition between viruses and/or their hosts could maintain toxin diversity. We propose that competitive interactions among chronic viruses to promote their host fitness form the basis of virus–host mutualism. This article is part of the theme issue ‘The secret lives of microbial mobile genetic elements’. The Royal Society 2022-01-17 2021-11-29 /pmc/articles/PMC8628083/ /pubmed/34839697 http://dx.doi.org/10.1098/rstb.2020.0476 Text en © 2021 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Articles
DeWerff, Samantha J.
Zhang, Changyi
Schneider, John
Whitaker, Rachel J.
Intraspecific antagonism through viral toxin encoded by chronic Sulfolobus spindle-shaped virus
title Intraspecific antagonism through viral toxin encoded by chronic Sulfolobus spindle-shaped virus
title_full Intraspecific antagonism through viral toxin encoded by chronic Sulfolobus spindle-shaped virus
title_fullStr Intraspecific antagonism through viral toxin encoded by chronic Sulfolobus spindle-shaped virus
title_full_unstemmed Intraspecific antagonism through viral toxin encoded by chronic Sulfolobus spindle-shaped virus
title_short Intraspecific antagonism through viral toxin encoded by chronic Sulfolobus spindle-shaped virus
title_sort intraspecific antagonism through viral toxin encoded by chronic sulfolobus spindle-shaped virus
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8628083/
https://www.ncbi.nlm.nih.gov/pubmed/34839697
http://dx.doi.org/10.1098/rstb.2020.0476
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