<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sullivan SA</submitter><funding>Chang Gung Memorial Hospital, Linkou (Linkou Chang Gung Memorial Hospital)</funding><funding>U.S. Department of Health &amp; Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID)</funding><pagination>6487</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12289875</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(1)</volume><pubmed_abstract>Trichomonas vaginalis, the causative agent of the venereal disease trichomoniasis, infects men and women globally and is associated with serious outcomes during pregnancy, increased risk of HIV-1 infection, and cancers of the human reproductive tract. Species of trichomonad parasitize a range of hosts in addition to humans, including birds, livestock, and pets. Genetic analysis of trichomonads recovered from columbid birds has provided evidence that they undergo frequent host-switching, and that a spillover event from columbids likely gave rise to T. vaginalis in humans. Here we describe a comparative genomics study of seven trichomonad species, generating chromosome-scale reference genomes for T. vaginalis and its avian sister species Trichomonas stableri, and assemblies of five other spe</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Comparative genomics of the parasite Trichomonas vaginalis reveals genes involved in spillover from birds to humans.</pubmed_title><pmcid>PMC12289875</pmcid><funding_grant_id>R21AI149449</funding_grant_id><funding_grant_id>CMRPD1M0571-2</funding_grant_id><funding_grant_id>U24AI183870</funding_grant_id><pubmed_authors>Liu H</pubmed_authors><pubmed_authors>Chandler C</pubmed_authors><pubmed_authors>Peters A</pubmed_authors><pubmed_authors>Chiu CH</pubmed_authors><pubmed_authors>Rogers KH</pubmed_authors><pubmed_authors>Srivastava H</pubmed_authors><pubmed_authors>Lee H</pubmed_authors><pubmed_authors>Schatz MC</pubmed_authors><pubmed_authors>Chen TW</pubmed_authors><pubmed_authors>Callejas-Hernandez F</pubmed_authors><pubmed_authors>Raidal SR</pubmed_authors><pubmed_authors>Liachko I</pubmed_authors><pubmed_authors>Tang P</pubmed_authors><pubmed_authors>Berenberg D</pubmed_authors><pubmed_authors>Mangelson H</pubmed_authors><pubmed_authors>Yeh YM</pubmed_authors><pubmed_authors>Carlton JM</pubmed_authors><pubmed_authors>Ranallo-Benavidez TR</pubmed_authors><pubmed_authors>Girard YA</pubmed_authors><pubmed_authors>Bonneau RA</pubmed_authors><pubmed_authors>Sullivan SA</pubmed_authors><pubmed_authors>Lee CC</pubmed_authors><pubmed_authors>Johnson CK</pubmed_authors><pubmed_authors>Gerhold R</pubmed_authors><pubmed_authors>Huang PJ</pubmed_authors><pubmed_authors>Orosco JC</pubmed_authors><pubmed_authors>Blow F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Comparative genomics of the parasite Trichomonas vaginalis reveals genes involved in spillover from birds to humans.</name><description>Trichomonas vaginalis, the causative agent of the venereal disease trichomoniasis, infects men and women globally and is associated with serious outcomes during pregnancy, increased risk of HIV-1 infection, and cancers of the human reproductive tract. Species of trichomonad parasitize a range of hosts in addition to humans, including birds, livestock, and pets. Genetic analysis of trichomonads recovered from columbid birds has provided evidence that they undergo frequent host-switching, and that a spillover event from columbids likely gave rise to T. vaginalis in humans. Here we describe a comparative genomics study of seven trichomonad species, generating chromosome-scale reference genomes for T. vaginalis and its avian sister species Trichomonas stableri, and assemblies of five other spe</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jul</publication><modification>2026-03-15T16:59:34.72Z</modification><creation>2025-08-13T03:04:33.665Z</creation></dates><accession>S-EPMC12289875</accession><cross_references><pubmed>40707449</pubmed><doi>10.1038/s41467-025-61483-w</doi></cross_references></HashMap>