<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Oka T</submitter><funding>Ministry of Health, Labour and Welfare</funding><funding>Japan Agency for Medical Research and Development</funding><funding>SHIONOGI INFECTIOUS DISEASE RESEARCH PROMOTION FOUNDATION</funding><funding>Japan Society for the Promotion of Science</funding><pagination>e0132525</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12646008</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>99(11)</volume><pubmed_abstract>Human sapoviruses (HuSaVs), which cause acute gastroenteritis, are highly diverse. Fifteen HuSaV genotype strains (GI.1-7, GII.1-5, -8, and GV.1-2) were efficiently propagated in the human duodenum-derived cell line HuTu80 when supplemented with conjugated bile acid (T. Oka, T.-C. Li, K. Yonemitsu, Y. Ami, et al., J Virol 98:e00639-24, 2024, https://doi.org/10.1128/jvi.00639-24). However, the host cellular factors involved in HuSaV infection and propagation remain unidentified. Using a knockout approach, we newly identified and confirmed that CD36 is a critical cellular protein for the propagation of all 15 HuSaV genotypes tested in HuTu80 cells. When the CD36 gene was re-expressed in CD36 gene knockout HuTu80 cells, all HuSaV genotype strains, except for GI.6 and GII.3, recovered their vi</pubmed_abstract><journal>Journal of virology</journal><pubmed_title>CD36 is required for human sapovirus propagation.</pubmed_title><pmcid>PMC12646008</pmcid><funding_grant_id>JP23fk0108683</funding_grant_id><funding_grant_id>JP23K21362</funding_grant_id><funding_grant_id>JP24K13428</funding_grant_id><funding_grant_id>JPMH22KA1001</funding_grant_id><funding_grant_id>JPMH25KA1001</funding_grant_id><funding_grant_id>JP20K08320</funding_grant_id><pubmed_authors>Takagi H</pubmed_authors><pubmed_authors>Oka T</pubmed_authors><pubmed_authors>Okemoto-Nakamura Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>CD36 is required for human sapovirus propagation.</name><description>Human sapoviruses (HuSaVs), which cause acute gastroenteritis, are highly diverse. Fifteen HuSaV genotype strains (GI.1-7, GII.1-5, -8, and GV.1-2) were efficiently propagated in the human duodenum-derived cell line HuTu80 when supplemented with conjugated bile acid (T. Oka, T.-C. Li, K. Yonemitsu, Y. Ami, et al., J Virol 98:e00639-24, 2024, https://doi.org/10.1128/jvi.00639-24). However, the host cellular factors involved in HuSaV infection and propagation remain unidentified. Using a knockout approach, we newly identified and confirmed that CD36 is a critical cellular protein for the propagation of all 15 HuSaV genotypes tested in HuTu80 cells. When the CD36 gene was re-expressed in CD36 gene knockout HuTu80 cells, all HuSaV genotype strains, except for GI.6 and GII.3, recovered their vi</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Nov</publication><modification>2026-06-05T19:07:39.388Z</modification><creation>2026-05-20T03:14:51.077Z</creation></dates><accession>S-EPMC12646008</accession><cross_references><pubmed>41190813</pubmed><doi>10.1128/jvi.01325-25</doi></cross_references></HashMap>