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Walleye dermal sarcoma virus Orf C: a potential oncolytic therapy

dc.contributor.authorMagden, Elizabeth, author
dc.contributor.authorQuackenbush, Sandra, advisor
dc.contributor.authorVandeWoude, Sue, committee member
dc.contributor.authorBiller, Barbara, committee member
dc.date.accessioned2007-01-03T05:34:13Z
dc.date.available2007-01-03T05:34:13Z
dc.date.issued2011
dc.description.abstractThe taxonomy and nomenclature of the North American weevil genus Thecesternus Say was reviewed. Five previously described species are recognized as valid: affinis, foveolatus, hirsutus, humeralis, and maculosus. One new species, tumulosus, from Texas is described as new. The following new synonymy is proposed: longior LeConte 1856 (= affinis LeConte 1856) and albidus Pierce 1909 (= maculosus Pierce 1909). A neotype is designated for T. humeralis (Say). A key to identify the species is provided, with various illustrations of key morphological features characterizing these species. Additionally, distribution maps, species descriptions, and species differentiation for each species is provided. A cladistic hypothesis of the included species is presented. Walleye dermal sarcoma virus (WDSV) is a complex retrovirus that causes the growth of multifocal, cutaneous tumors in walleye fish (Sander vitreus vitreus). These virus-induced tumors spontaneously regress on a seasonal basis. The WDSV genome encodes three accessory proteins (rv-cyclin, Orf B, and Orf C) that are necessary for regulation of virus expression, tumor formation, and tumor regression. While rv-cyclin and B are critical for tumor development, Orf C contributes to the observed seasonal tumor regression. Previous studies have shown that Orf C targets the cell mitochondria and induces apoptosis. These studies suggest that Orf C-induced apoptosis leads to the observed tumor regression in fish infected with WDSV. To further define the mechanism(s) of apoptosis, we generated a recombinant lentivirus (Lenti Orf C) that expresses WDSV Orf C. By infecting cells with Lenti Orf C, we showed decreasing cell viability in association with increasing virus concentrations. We also demonstrated Orf C expression in mitochondrial, cytosolic, and nuclear cell fractions, with the strongest Orf C expression in cell nuclei. In addition, we identified two pro-apoptotic proteins that associate with Orf C, ANT and Bax, and identified a third protein, AIF, as a potential Orf C target. While significant progress has been made in elucidating the mechanism(s) of Orf C-induced apoptosis, further studies are necessary to determine which cellular proteins are the primary targets of Orf C. These apoptosis-inducing Orf C targets may be useful in developing future oncolytic therapies.
dc.format.mediumborn digital
dc.format.mediummasters theses
dc.identifierMagden_colostate_0053N_10532.pdf
dc.identifier.urihttp://hdl.handle.net/10217/48116
dc.languageEnglish
dc.language.isoeng
dc.publisherColorado State University. Libraries
dc.relation.ispartof2000-2019
dc.rightsCopyright and other restrictions may apply. User is responsible for compliance with all applicable laws. For information about copyright law, please see https://libguides.colostate.edu/copyright.
dc.subjectdermal sarcoma
dc.subjectWDSV
dc.subjectwalleye
dc.subjectOrf C
dc.subjectoncolytic
dc.titleWalleye dermal sarcoma virus Orf C: a potential oncolytic therapy
dc.typeText
dcterms.rights.dplaThis Item is protected by copyright and/or related rights (https://rightsstatements.org/vocab/InC/1.0/). You are free to use this Item in any way that is permitted by the copyright and related rights legislation that applies to your use. For other uses you need to obtain permission from the rights-holder(s).
thesis.degree.disciplineMicrobiology, Immunology, and Pathology
thesis.degree.grantorColorado State University
thesis.degree.levelMasters
thesis.degree.nameMaster of Science (M.S.)

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