Persistent reovirus RNA, in the absence of detectable infectious reovirus, is associated with the progression of biliary atresia in neonatal mice / by Jennifer Aleisa Lewis.

Author/creator Lewis, Jennifer Aleisa author.
Other author Oberhaus, Stephanie M., degree supervisor.
Other author East Carolina University. Department of Biology.
Format Theses and dissertations
Production2000.
Description78 leaves : illustrations (some color) ; 29 cm
Supplemental ContentAccess via ScholarShip
Subjects

Summary Extrahepatic biliary atresia (EHBA) is a serious disease causing blockage of bile ducts, liver damage, and eventually death in young children. The cause of EHBA is unknown and the only two available treatments are costly and not highly effective. Reovirus serotype 3 infection of neonatal mice has been shown to produce symptoms like those of human EHBA, and is a well-characterized system for studying viral pathogenesis, identifying it as a potentially useful animal system in which to study this disease. Reovirus has been shown to induce apoptosis in mouse tissues, suggesting it as a mechanism for tissue destruction and the production of disease. We have previously shown that, following peroral inoculation of with reovirus T3A, mice with biliary atresia have significant tissue damage and apoptosis localized to portal triad regions of the liver after peak viral titer has been reached, and often when infectious virus can no longer be detected by immunofluorescence or in situ hybridization. Using reverse transcriptase-polymerase chain reaction (RT-PCR), others have detected reovirus in the livers of mice 50 days post-infection, long after infectious virus is no longer detectable. In order to determine whether or not reovirus RNA persisted in the livers of mice with biliary atresia, in the absence of detectable infectious virus, a nested RT-PCR was used for detecting reovirus LI RNA. Reovirus LI RNA was found in the absence of detectable infectious virus, when liver tissue damage and apoptosis associated with biliary atresia were at their peak. These data suggest that persistent reovirus RNA is associated with the progression of this disease in mice.
General noteSubmitted to the faculty of the Department of Biology.
General noteAdvisor: Stephanie Oberhaus
Dissertation noteM.S. East Carolina University 2000
Bibliography noteIncludes bibliographical references (leaves 73-78).
Genre/formAcademic theses.
Genre/formAcademic theses.
Genre/formThèses et écrits académiques.

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