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The novel anti-phage system Shield co-opts an RmuC domain to mediate phage defense across Pseudomonas species

Competitive bacteria-bacteriophage interactions have resulted in the evolution of a plethora of bacterial defense systems preventing phage propagation. In recent years, computational and bioinformatic approaches have underpinned the discovery of numerous novel bacterial defense systems. Anti-phage s...

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Autores principales: Macdonald, Elliot, Wright, Rosanna, Connolly, James P. R., Strahl, Henrik, Brockhurst, Michael, van Houte, Stineke, Blower, Tim R., Palmer, Tracy, Mariano, Giuseppina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10270631/
https://www.ncbi.nlm.nih.gov/pubmed/37276233
http://dx.doi.org/10.1371/journal.pgen.1010784
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author Macdonald, Elliot
Wright, Rosanna
Connolly, James P. R.
Strahl, Henrik
Brockhurst, Michael
van Houte, Stineke
Blower, Tim R.
Palmer, Tracy
Mariano, Giuseppina
author_facet Macdonald, Elliot
Wright, Rosanna
Connolly, James P. R.
Strahl, Henrik
Brockhurst, Michael
van Houte, Stineke
Blower, Tim R.
Palmer, Tracy
Mariano, Giuseppina
author_sort Macdonald, Elliot
collection PubMed
description Competitive bacteria-bacteriophage interactions have resulted in the evolution of a plethora of bacterial defense systems preventing phage propagation. In recent years, computational and bioinformatic approaches have underpinned the discovery of numerous novel bacterial defense systems. Anti-phage systems are frequently encoded together in genomic loci termed defense islands. Here we report the identification and characterisation of a novel anti-phage system, that we have termed Shield, which forms part of the Pseudomonas defensive arsenal. The Shield system comprises the core component ShdA, a membrane-bound protein harboring an RmuC domain. Heterologous production of ShdA alone is sufficient to mediate bacterial immunity against several phages. We demonstrate that Shield and ShdA confer population-level immunity and that they can also decrease transformation efficiency. We further show that ShdA homologues can degrade DNA in vitro and, when expressed in a heterologous host, can alter the organisation of the host chromosomal DNA. Use of comparative genomic approaches identified how Shield can be divided into four subtypes, three of which contain additional components that in some cases can negatively affect the activity of ShdA and/or provide additional lines of phage defense. Collectively, our results identify a new player within the Pseudomonas bacterial immunity arsenal that displays a novel mechanism of protection, and reveals a role for RmuC domains in phage defense.
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spelling pubmed-102706312023-06-16 The novel anti-phage system Shield co-opts an RmuC domain to mediate phage defense across Pseudomonas species Macdonald, Elliot Wright, Rosanna Connolly, James P. R. Strahl, Henrik Brockhurst, Michael van Houte, Stineke Blower, Tim R. Palmer, Tracy Mariano, Giuseppina PLoS Genet Research Article Competitive bacteria-bacteriophage interactions have resulted in the evolution of a plethora of bacterial defense systems preventing phage propagation. In recent years, computational and bioinformatic approaches have underpinned the discovery of numerous novel bacterial defense systems. Anti-phage systems are frequently encoded together in genomic loci termed defense islands. Here we report the identification and characterisation of a novel anti-phage system, that we have termed Shield, which forms part of the Pseudomonas defensive arsenal. The Shield system comprises the core component ShdA, a membrane-bound protein harboring an RmuC domain. Heterologous production of ShdA alone is sufficient to mediate bacterial immunity against several phages. We demonstrate that Shield and ShdA confer population-level immunity and that they can also decrease transformation efficiency. We further show that ShdA homologues can degrade DNA in vitro and, when expressed in a heterologous host, can alter the organisation of the host chromosomal DNA. Use of comparative genomic approaches identified how Shield can be divided into four subtypes, three of which contain additional components that in some cases can negatively affect the activity of ShdA and/or provide additional lines of phage defense. Collectively, our results identify a new player within the Pseudomonas bacterial immunity arsenal that displays a novel mechanism of protection, and reveals a role for RmuC domains in phage defense. Public Library of Science 2023-06-05 /pmc/articles/PMC10270631/ /pubmed/37276233 http://dx.doi.org/10.1371/journal.pgen.1010784 Text en © 2023 Macdonald et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Macdonald, Elliot
Wright, Rosanna
Connolly, James P. R.
Strahl, Henrik
Brockhurst, Michael
van Houte, Stineke
Blower, Tim R.
Palmer, Tracy
Mariano, Giuseppina
The novel anti-phage system Shield co-opts an RmuC domain to mediate phage defense across Pseudomonas species
title The novel anti-phage system Shield co-opts an RmuC domain to mediate phage defense across Pseudomonas species
title_full The novel anti-phage system Shield co-opts an RmuC domain to mediate phage defense across Pseudomonas species
title_fullStr The novel anti-phage system Shield co-opts an RmuC domain to mediate phage defense across Pseudomonas species
title_full_unstemmed The novel anti-phage system Shield co-opts an RmuC domain to mediate phage defense across Pseudomonas species
title_short The novel anti-phage system Shield co-opts an RmuC domain to mediate phage defense across Pseudomonas species
title_sort novel anti-phage system shield co-opts an rmuc domain to mediate phage defense across pseudomonas species
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10270631/
https://www.ncbi.nlm.nih.gov/pubmed/37276233
http://dx.doi.org/10.1371/journal.pgen.1010784
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