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Tandem mobilization of anti-phage defenses alongside SCCmec cassettes

Bacterial viruses (phages) and the immune systems targeted against them significantly impact bacterial survival, evolution, and the emergence of pathogenic strains. While recent research has made spectacular strides towards discovering and validating new defenses in a few model organisms(1–3), the i...

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Autores principales: Hossain, Motaher, Aslan, Barbaros, Hatoum-Aslan, Asma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10055296/
https://www.ncbi.nlm.nih.gov/pubmed/36993521
http://dx.doi.org/10.1101/2023.03.17.533233
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author Hossain, Motaher
Aslan, Barbaros
Hatoum-Aslan, Asma
author_facet Hossain, Motaher
Aslan, Barbaros
Hatoum-Aslan, Asma
author_sort Hossain, Motaher
collection PubMed
description Bacterial viruses (phages) and the immune systems targeted against them significantly impact bacterial survival, evolution, and the emergence of pathogenic strains. While recent research has made spectacular strides towards discovering and validating new defenses in a few model organisms(1–3), the inventory of immune systems in clinically-relevant bacteria remains underexplored, and little is known about the mechanisms by which these systems horizontally spread. Such pathways not only impact the evolutionary trajectory of bacterial pathogens, but also threaten to undermine the effectiveness of phage-based therapeutics. Here, we investigate the battery of defenses in staphylococci, opportunistic pathogens that constitute leading causes of antibiotic-resistant infections. We show that these organisms harbor a variety of anti-phage defenses encoded within/near the infamous SCC (staphylococcal cassette chromosome) mec cassettes, mobile genomic islands that confer methicillin resistance. Importantly, we demonstrate that SCCmec-encoded recombinases mobilize not only SCCmec, but also tandem cassettes enriched with diverse defenses. Further, we show that phage infection potentiates cassette mobilization. Taken together, our findings reveal that beyond spreading antibiotic resistance, SCCmec cassettes play a central role in disseminating anti-phage defenses. This work underscores the urgent need for developing adjunctive treatments that target this pathway to save the burgeoning phage therapeutics from suffering the same fate as conventional antibiotics.
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spelling pubmed-100552962023-03-30 Tandem mobilization of anti-phage defenses alongside SCCmec cassettes Hossain, Motaher Aslan, Barbaros Hatoum-Aslan, Asma bioRxiv Article Bacterial viruses (phages) and the immune systems targeted against them significantly impact bacterial survival, evolution, and the emergence of pathogenic strains. While recent research has made spectacular strides towards discovering and validating new defenses in a few model organisms(1–3), the inventory of immune systems in clinically-relevant bacteria remains underexplored, and little is known about the mechanisms by which these systems horizontally spread. Such pathways not only impact the evolutionary trajectory of bacterial pathogens, but also threaten to undermine the effectiveness of phage-based therapeutics. Here, we investigate the battery of defenses in staphylococci, opportunistic pathogens that constitute leading causes of antibiotic-resistant infections. We show that these organisms harbor a variety of anti-phage defenses encoded within/near the infamous SCC (staphylococcal cassette chromosome) mec cassettes, mobile genomic islands that confer methicillin resistance. Importantly, we demonstrate that SCCmec-encoded recombinases mobilize not only SCCmec, but also tandem cassettes enriched with diverse defenses. Further, we show that phage infection potentiates cassette mobilization. Taken together, our findings reveal that beyond spreading antibiotic resistance, SCCmec cassettes play a central role in disseminating anti-phage defenses. This work underscores the urgent need for developing adjunctive treatments that target this pathway to save the burgeoning phage therapeutics from suffering the same fate as conventional antibiotics. Cold Spring Harbor Laboratory 2023-03-18 /pmc/articles/PMC10055296/ /pubmed/36993521 http://dx.doi.org/10.1101/2023.03.17.533233 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Hossain, Motaher
Aslan, Barbaros
Hatoum-Aslan, Asma
Tandem mobilization of anti-phage defenses alongside SCCmec cassettes
title Tandem mobilization of anti-phage defenses alongside SCCmec cassettes
title_full Tandem mobilization of anti-phage defenses alongside SCCmec cassettes
title_fullStr Tandem mobilization of anti-phage defenses alongside SCCmec cassettes
title_full_unstemmed Tandem mobilization of anti-phage defenses alongside SCCmec cassettes
title_short Tandem mobilization of anti-phage defenses alongside SCCmec cassettes
title_sort tandem mobilization of anti-phage defenses alongside sccmec cassettes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10055296/
https://www.ncbi.nlm.nih.gov/pubmed/36993521
http://dx.doi.org/10.1101/2023.03.17.533233
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