CHARACTERIZATION OF BORRELIA BURGDORFERI GENE PRODUCTS CRITICAL FOR PATHOGEN PERSISTENCE AND TRANSMISSION

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dc.contributor.advisorPAL, UTPALen_US
dc.contributor.authorKUMAR, MANISHen_US
dc.contributor.departmentVeterinary Medical Scienceen_US
dc.contributor.publisherDigital Repository at the University of Marylanden_US
dc.contributor.publisherUniversity of Maryland (College Park, Md.)en_US
dc.date.accessioned2011-02-19T07:00:01Z
dc.date.available2011-02-19T07:00:01Z
dc.date.issued2010en_US
dc.description.abstractThe pathogen of Lyme disease, <italic>Borrelia burgdorferi</italic>, persists in a natural tick-rodent infection cycle. An assessment of microbial transcriptome <italic>in vivo</italic> encoding selected membrane proteins shows that<italic> bba52</italic> is upregulated during pathogen transmission. Deletion of <italic>bba52</italic> in infectious <italic>B. burgdorferi</italic> did not alter the outcome of murine inflammation or long-term pathogen persistence in mice or ticks. However, the <italic>bba52</italic> mutant was impaired for transmission between feeding ticks and mice, phenotypic defects that could be rescued when <italic>bba52</italic> was genetically restored to the original genomic locus. I show that BBA52 is a surface-exposed outer membrane protein. As BBA52 is highly immunogenic, I next assessed whether BBA52 could serve as a potential candidate for transmission-blocking vaccines against spirochete infection. Passive transfer of BBA52 antibodies into the ticks did not interfere with microbial persistence in unfed ticks but blocked pathogen transmission from feeding ticks to murine hosts. More importantly, active immunization of mice with recombinant BBA52 protein significantly blocked <italic>B. burgdorferi</italic> transmission from ticks to naïve murine hosts. As BBA52 antibodies lacked detectable borreliacidal activities, their interference with spirochete survival <italic>in vivo</italic> could result from the inhibition of BBA52 function, such as vector-pathogen interaction. By far-western analysis using tick gut proteins, I found that BBA52 interacts with a ~ 35 kDa tick gut protein. I also show that BBA52 forms distinct homo-oligomer in borrelial cells and also interacts with two proteins of <italic>B. burgdorferi</italic>. These BBA52 interacting proteins possess approximate molecular weight of 33 kDa and 25 kDa and are located in the outer membrane and protoplasm, respectively. Taken together, these studies suggested the remarkable existence of <italic>B. burgdorferi</italic> surface antigens that are differentially expressed <italic>in vivo</italic> and support microbial transitions between hosts and the vector. Identification and characterization of novel vector-specific and feeding induced borrelial antigens could contribute to the development of transmission-blocking vaccines against Lyme disease.en_US
dc.identifier.urihttp://hdl.handle.net/1903/11182
dc.subject.pqcontrolledVeterinary Medicineen_US
dc.subject.pquncontrolledBACTERIAen_US
dc.subject.pquncontrolledBORRELIAen_US
dc.subject.pquncontrolledDISEASEen_US
dc.subject.pquncontrolledLYMEen_US
dc.subject.pquncontrolledPROTEINen_US
dc.subject.pquncontrolledVACCINEen_US
dc.titleCHARACTERIZATION OF BORRELIA BURGDORFERI GENE PRODUCTS CRITICAL FOR PATHOGEN PERSISTENCE AND TRANSMISSIONen_US
dc.typeDissertationen_US

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