<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Massey JH</submitter><funding>NIAID NIH HHS</funding><funding>National Institutes of Health</funding><funding>National Science Foundation</funding><pagination>185-198</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8742837</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>30(2)</volume><pubmed_abstract>Bacterial endosymbionts induce dramatic phenotypes in their arthropod hosts, including cytoplasmic incompatibility, feminization, parthenogenesis, male killing, parasitoid defense, and pathogen blocking. The molecular mechanisms underlying these effects remain largely unknown but recent evidence suggests that protein toxins secreted by the endosymbionts play a role. Here, we describe the diversity and function of endosymbiont proteins with homology to known bacterial toxins. We focus on maternally transmitted endosymbionts belonging to the Wolbachia, Rickettsia, Arsenophonus, Hamiltonella, Spiroplasma, and Cardinium genera because of their ability to induce the above phenotypes. We identify at least 16 distinct toxin families with diverse enzymatic activities, including AMPylases, nucleases, proteases, and glycosyltransferases. Notably, several annotated toxins contain domains with homology to eukaryotic proteins, suggesting that arthropod endosymbionts mimic host biochemistry to manipulate host physiology, similar to bacterial pathogens.</pubmed_abstract><journal>Trends in microbiology</journal><pubmed_title>Diversity and function of arthropod endosymbiont toxins.</pubmed_title><pmcid>PMC8742837</pmcid><funding_grant_id>BII 2022049</funding_grant_id><funding_grant_id>R01AI144430</funding_grant_id><funding_grant_id>R01 AI144430</funding_grant_id><pubmed_authors>Newton ILG</pubmed_authors><pubmed_authors>Massey JH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Diversity and function of arthropod endosymbiont toxins.</name><description>Bacterial endosymbionts induce dramatic phenotypes in their arthropod hosts, including cytoplasmic incompatibility, feminization, parthenogenesis, male killing, parasitoid defense, and pathogen blocking. The molecular mechanisms underlying these effects remain largely unknown but recent evidence suggests that protein toxins secreted by the endosymbionts play a role. Here, we describe the diversity and function of endosymbiont proteins with homology to known bacterial toxins. We focus on maternally transmitted endosymbionts belonging to the Wolbachia, Rickettsia, Arsenophonus, Hamiltonella, Spiroplasma, and Cardinium genera because of their ability to induce the above phenotypes. We identify at least 16 distinct toxin families with diverse enzymatic activities, including AMPylases, nucleases, proteases, and glycosyltransferases. Notably, several annotated toxins contain domains with homology to eukaryotic proteins, suggesting that arthropod endosymbionts mimic host biochemistry to manipulate host physiology, similar to bacterial pathogens.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Feb</publication><modification>2024-11-20T12:13:40.319Z</modification><creation>2024-11-20T12:13:40.319Z</creation></dates><accession>S-EPMC8742837</accession><cross_references><pubmed>34253453</pubmed><doi>10.1016/j.tim.2021.06.008</doi></cross_references></HashMap>