<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lee Q</submitter><funding>NIAID NIH HHS</funding><funding>NCI NIH HHS</funding><pagination>e1008262</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6999912</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(1)</volume><pubmed_abstract>Mouse kidney parvovirus (MKPV) is a member of the provisional genus Chapparvovirus that causes renal disease in immune-compromised mice, with a disease course reminiscent of polyomavirus-associated nephropathy in immune-suppressed kidney transplant patients. Here we map four major MKPV transcripts, created by alternative splicing, to a common initiator region, and use mass spectrometry to identify "p10" and "p15" as novel chapparvovirus accessory proteins produced in MKPV-infected kidneys. p15 and the splicing-dependent putative accessory protein NS2 are conserved in all near-complete amniote chapparvovirus genomes currently available (from mammals, birds and a reptile). In contrast, p10 may be encoded only by viruses with >60% amino acid identity to MKPV. We show that MKPV is kidney-tropi</pubmed_abstract><journal>PLoS pathogens</journal><pubmed_title>Murine and related chapparvoviruses are nephro-tropic and produce novel accessory proteins in infected kidneys.</pubmed_title><pmcid>PMC6999912</pmcid><funding_grant_id>P30 CA008748</funding_grant_id><funding_grant_id>U19 AI109761</funding_grant_id><pubmed_authors>Lee Q</pubmed_authors><pubmed_authors>Brenner O</pubmed_authors><pubmed_authors>Pinello N</pubmed_authors><pubmed_authors>Padula MP</pubmed_authors><pubmed_authors>Shaban B</pubmed_authors><pubmed_authors>Monette S</pubmed_authors><pubmed_authors>Crim MJ</pubmed_authors><pubmed_authors>Roediger B</pubmed_authors><pubmed_authors>Wong JJ</pubmed_authors><pubmed_authors>O'Rourke MB</pubmed_authors><pubmed_authors>Jolly CJ</pubmed_authors><pubmed_authors>Weninger W</pubmed_authors><pubmed_authors>Song R</pubmed_authors><pubmed_authors>Souza WM</pubmed_authors><pubmed_authors>Pimanda JE</pubmed_authors><pubmed_authors>Williams SH</pubmed_authors><pubmed_authors>Fumagalli MJ</pubmed_authors><pubmed_authors>Orkin JD</pubmed_authors><pubmed_authors>Melin AD</pubmed_authors></additional><is_claimable>false</is_claimable><name>Murine and related chapparvoviruses are nephro-tropic and produce novel accessory proteins in infected kidneys.</name><description>Mouse kidney parvovirus (MKPV) is a member of the provisional genus Chapparvovirus that causes renal disease in immune-compromised mice, with a disease course reminiscent of polyomavirus-associated nephropathy in immune-suppressed kidney transplant patients. Here we map four major MKPV transcripts, created by alternative splicing, to a common initiator region, and use mass spectrometry to identify "p10" and "p15" as novel chapparvovirus accessory proteins produced in MKPV-infected kidneys. p15 and the splicing-dependent putative accessory protein NS2 are conserved in all near-complete amniote chapparvovirus genomes currently available (from mammals, birds and a reptile). In contrast, p10 may be encoded only by viruses with >60% amino acid identity to MKPV. We show that MKPV is kidney-tropi</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jan</publication><modification>2026-05-07T00:38:07.089Z</modification><creation>2020-05-22T10:32:32Z</creation></dates><accession>S-EPMC6999912</accession><cross_references><pubmed>31971979</pubmed><doi>10.1371/journal.ppat.1008262</doi></cross_references></HashMap>