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dc.contributor.authorBrown, David W.
dc.contributor.authorWelsh, Raymond M.
dc.contributor.authorLike, Arthur A.
dc.date2022-08-11T08:09:34.000
dc.date.accessioned2022-08-23T16:36:04Z
dc.date.available2022-08-23T16:36:04Z
dc.date.issued1993-10-01
dc.date.submitted2009-03-26
dc.identifier.citationJ Virol. 1993 Oct;67(10):5873-8.
dc.identifier.issn0022-538X (Print)
dc.identifier.pmid8371347
dc.identifier.urihttp://hdl.handle.net/20.500.14038/38703
dc.description.abstractA parvovirus serologically identified as Kilham rat virus (KRV) reproducibly induces acute type I diabetes in diabetes-resistant BB/Wor rats. The tissue tropism of KRV was investigated by in situ hybridization with a digoxigenin-labelled plasmid DNA probe containing approximately 1.6 kb of the genome of the UMass isolate of KRV. Partial sequencing of the KRV probe revealed high levels of homology to the sequence of minute virus of mice (89%) and to the sequence of H1 (99%), a parvovirus capable of infecting rats and humans. Of the 444 bases sequenced, 440 were shared by H1. KRV mRNA and DNA were readily detected in lymphoid tissues 5 days postinfection but were seldom seen in the pancreas. High levels of viral nucleic acids were observed in the thymus, spleen, and peripancreatic and cervical lymph nodes. The low levels of infection observed in the pancreas involved essentially only endothelial and interstitial cells. Beta cells of the pancreas were not infected with KRV. These findings suggest that widespread infection of peripancreatic and other lymphoid tissues but not pancreatic beta cells by KRV triggers autoimmune diabetes by perturbing the immune system of genetically predisposed BB/Wor rats.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=8371347&dopt=Abstract">Link to Article in PubMed</a>
dc.subjectAnimals
dc.subjectBase Sequence
dc.subjectCell Line
dc.subjectDNA Probes
dc.subjectDNA, Viral
dc.subjectDiabetes Mellitus, Type 1
dc.subjectIn Situ Hybridization
dc.subjectIslets of Langerhans
dc.subjectKidney
dc.subjectLymph Nodes
dc.subjectMolecular Sequence Data
dc.subjectParvoviridae
dc.subjectRNA, Messenger
dc.subjectRNA, Viral
dc.subjectRats
dc.subjectRats, Inbred BB
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleInfection of peripancreatic lymph nodes but not islets precedes Kilham rat virus-induced diabetes in BB/Wor rats
dc.typeJournal Article
dc.source.journaltitleJournal of virology
dc.source.volume67
dc.source.issue10
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=2556&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/1557
dc.identifier.contextkey798534
refterms.dateFOA2022-08-23T16:36:04Z
html.description.abstract<p>A parvovirus serologically identified as Kilham rat virus (KRV) reproducibly induces acute type I diabetes in diabetes-resistant BB/Wor rats. The tissue tropism of KRV was investigated by in situ hybridization with a digoxigenin-labelled plasmid DNA probe containing approximately 1.6 kb of the genome of the UMass isolate of KRV. Partial sequencing of the KRV probe revealed high levels of homology to the sequence of minute virus of mice (89%) and to the sequence of H1 (99%), a parvovirus capable of infecting rats and humans. Of the 444 bases sequenced, 440 were shared by H1. KRV mRNA and DNA were readily detected in lymphoid tissues 5 days postinfection but were seldom seen in the pancreas. High levels of viral nucleic acids were observed in the thymus, spleen, and peripancreatic and cervical lymph nodes. The low levels of infection observed in the pancreas involved essentially only endothelial and interstitial cells. Beta cells of the pancreas were not infected with KRV. These findings suggest that widespread infection of peripancreatic and other lymphoid tissues but not pancreatic beta cells by KRV triggers autoimmune diabetes by perturbing the immune system of genetically predisposed BB/Wor rats.</p>
dc.identifier.submissionpathoapubs/1557
dc.contributor.departmentDepartment of Pathology
dc.source.pages5873-8


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