<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(8)</volume><submitter>Garrett SR</submitter><funding>Wellcome Trust</funding><funding>Biotechnology and Biological Sciences Research Council</funding><pubmed_abstract>The type VII secretion system (T7SS) is found in many Gram-positive firmicutes and secretes protein toxins that mediate bacterial antagonism. Two T7SS toxins have been identified in &lt;i>Staphylococcus aureus&lt;/i>, EsaD a nuclease toxin that is counteracted by the EsaG immunity protein, and TspA, which has membrane depolarising activity and is neutralised by TsaI. Both toxins are polymorphic, and strings of non-identical &lt;i>esaG&lt;/i> and &lt;i>tsaI&lt;/i> immunity genes are encoded in all &lt;i>S. aureus&lt;/i> strains. To investigate the evolution of &lt;i>esaG&lt;/i> repertoires, we analysed the sequences of the tandem &lt;i>esaG&lt;/i> genes and their encoded proteins. We identified three blocks of high sequence similarity shared by all &lt;i>esaG&lt;/i> genes and identified evidence of extensive recombination events be</pubmed_abstract><journal>Microbial genomics</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9484751</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Homologous recombination between tandem paralogues drives evolution of a subset of type VII secretion system immunity genes in firmicute bacteria.</pubmed_title><pmcid>PMC9484751</pmcid><funding_grant_id>218622/Z/19/Z</funding_grant_id><funding_grant_id>110183/A/15/Z</funding_grant_id><funding_grant_id>BB/M011186/1</funding_grant_id><funding_grant_id>101503/Z/13/Z</funding_grant_id><pubmed_authors>Palmer T</pubmed_authors><pubmed_authors>Dicks J</pubmed_authors><pubmed_authors>Mariano G</pubmed_authors><pubmed_authors>Garrett SR</pubmed_authors></additional><is_claimable>false</is_claimable><name>Homologous recombination between tandem paralogues drives evolution of a subset of type VII secretion system immunity genes in firmicute bacteria.</name><description>The type VII secretion system (T7SS) is found in many Gram-positive firmicutes and secretes protein toxins that mediate bacterial antagonism. Two T7SS toxins have been identified in &lt;i>Staphylococcus aureus&lt;/i>, EsaD a nuclease toxin that is counteracted by the EsaG immunity protein, and TspA, which has membrane depolarising activity and is neutralised by TsaI. Both toxins are polymorphic, and strings of non-identical &lt;i>esaG&lt;/i> and &lt;i>tsaI&lt;/i> immunity genes are encoded in all &lt;i>S. aureus&lt;/i> strains. To investigate the evolution of &lt;i>esaG&lt;/i> repertoires, we analysed the sequences of the tandem &lt;i>esaG&lt;/i> genes and their encoded proteins. We identified three blocks of high sequence similarity shared by all &lt;i>esaG&lt;/i> genes and identified evidence of extensive recombination events be</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Aug</publication><modification>2026-05-27T11:15:24.043Z</modification><creation>2024-12-04T07:50:37.449Z</creation></dates><accession>S-EPMC9484751</accession><cross_references><pubmed>35960642</pubmed><doi>10.1099/mgen.0.000868</doi></cross_references></HashMap>