The guinea pig as a model for genital chlamydial pathogenesis and vaccine development

dc.contributor.advisorArulanandam, Bernard P.
dc.contributor.authorWali, Shradha
dc.contributor.committeeMemberGuentzel, M. Neal
dc.contributor.committeeMemberChambers, James P.
dc.date.accessioned2024-03-08T17:36:23Z
dc.date.available2024-03-08T17:36:23Z
dc.date.issued2014
dc.descriptionThis item is available only to currently enrolled UTSA students, faculty or staff. To download, navigate to Log In in the top right-hand corner of this screen, then select Log in with my UTSA ID.
dc.description.abstractGenital Chlamydia trachomatis infections in humans can lead to severe tubal damage such as pelvic inflammatory disorder and infertility, if left untreated. Taking into consideration of the complications associated with C. trachomatis infection in women, it appears guinea pig model may more closely resemble human disease. We have established the Guinea Pig model with C. caviae and C. trachomatis D genital infections in our laboratory, where we have characterized the primary infection in the genital tract of Guinea Pigs. In this study, we evaluated host immune responses following genital guinea pig inclusion conjunctivitis (GPIC) agent (Chlamydia caviae) infection in intranasally C. caviae vaccinated guinea pigs. C. caviae -vaccinated guinea pigs resolved the genital tract infection as early as day 3 with reduced pathology, whereas mock-vaccinated animals shed C. caviae up to day 18 post-challenge with a greater degree of upper genital pathology at 80 days post-challenge. C. caviae -vaccinated animals displayed elevated levels of antigen specific IgG, IgG1 and IgG2 responses, able to neutralize GPIC in vitro. Using a guinea pig specific transcriptome RT-PCR array, we observed co-regulation of innate, Th2-humoral, and Th1-cellular/inflammatory immune genes following infection. The expression of these Th-1 and Th-2 associated genes was found to be higher in EB-vaccinated, compared to mock-vaccinated, animals at day 3 post challenge and correlated with early clearance of bacterial shedding. These findings were validated using single target qRT-PCRs, and provide evidence for guinea pig specific B and T cell related genes being activated at local sites of infection. This report adds to previous findings on the usefulness of this animal model to study chlamydial pathogenesis and test putative vaccine candidates against genital infection.
dc.description.departmentIntegrative Biology
dc.format.extent31 pages
dc.format.mimetypeapplication/pdf
dc.identifier.isbn9781303921346
dc.identifier.urihttps://hdl.handle.net/20.500.12588/6168
dc.languageen
dc.subjectChlamydia
dc.subjectGuinea pig
dc.subjectVaccine
dc.subject.classificationImmunology
dc.subject.lcshChlamydia trachomatis -- Pathogenesis
dc.subject.lcshGuinea pigs as laboratory animals
dc.titleThe guinea pig as a model for genital chlamydial pathogenesis and vaccine development
dc.typeThesis
dc.type.dcmiText
dcterms.accessRightspq_closed
thesis.degree.departmentIntegrative Biology
thesis.degree.grantorUniversity of Texas at San Antonio
thesis.degree.levelMasters
thesis.degree.nameMaster of Science

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