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Creating Live Attenuated HSV-2 Vaccine Candidate Strains Through Codon Pair Bias Deoptimization

dc.contributor.advisorDeStefano, Jeffreyen_US
dc.contributor.authorGodbout, Rachelen_US
dc.date.accessioned2016-02-06T06:46:01Z
dc.date.available2016-02-06T06:46:01Z
dc.date.issued2015en_US
dc.identifierhttps://doi.org/10.13016/M2V72K
dc.identifier.urihttp://hdl.handle.net/1903/17324
dc.description.abstractHerpes simplex virus 2 (HSV-2) is the primary causative agent of genital herpes, a disease characterized by painful recurrent anogenital lesions, higher risks for HIV and other STD transmissions, and potential childbirth complications. Despite the large medical burden of HSV-2, no vaccines are currently available. Most HSV-2 vaccine candidates have been subunit vaccines due to safety concerns, but live attenuated vaccines (LAVs) should be considered. Codon pair bias (CPB) is the phenomenon that specific codons pairs appear more frequently than expected. CPB deoptimization (CPBD) has been shown to significantly attenuate polio, influenza, and Streptococcus pneumoniae, indicating that CPBD is a viable attenuation method and LAV strategy. However, CPBD has never been used to attenuate DNA viruses, so its ability to attenuate these viruses remains unknown. This thesis describes the usage of CPBD to deoptimize specific HSV-2 genes to create potential HSV-2 LAV candidates.en_US
dc.language.isoenen_US
dc.titleCreating Live Attenuated HSV-2 Vaccine Candidate Strains Through Codon Pair Bias Deoptimizationen_US
dc.typeThesisen_US
dc.contributor.publisherDigital Repository at the University of Marylanden_US
dc.contributor.publisherUniversity of Maryland (College Park, Md.)en_US
dc.contributor.departmentCell Biology & Molecular Geneticsen_US
dc.subject.pqcontrolledVirologyen_US
dc.subject.pqcontrolledBiologyen_US
dc.subject.pquncontrolledcodon pair bias deoptimizationen_US
dc.subject.pquncontrolledgenital herpesen_US
dc.subject.pquncontrolledHSV-2en_US
dc.subject.pquncontrolledsynthetic attenuated virus engineeringen_US


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