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dc.contributor.authorSanjari, Salar
dc.date.accessioned2014-05-28T19:07:30Z
dc.date.available2014-12-16T17:19:40Z
dc.date.issued2014
dc.identifier.urihttp://hdl.handle.net/10713/4090
dc.descriptionUniversity of Maryland, Baltimore. Epidemiology and Preventive Medicine. M.S. 2014en_US
dc.description.abstractThe majority (65%) of human bacterial infections involve biofilms, a complex heterogeneous community of microorganisms. Staphylococcus aureus causes a broad range of local and systemic infectious diseases including chronic biofilm-associated infections. The high morbidity, mortality and the ever-increasing associated healthcare costs have persuaded scientists to search for a silver bullet. Furthermore, emergence of antibiotic resistance and associated financial justifications have convinced many researchers and pharmaceutical companies that a vaccination approach can be a far more effective preventive approach against staphylococcal infections. As such, many researchers have focused their efforts to develop a vaccine against the free-floating, planktonic, S. aureus. In a new approach, we evaluated the efficacy of a pentavalent vaccine with four biofilm and one planktonic specific recombinant antigen against S. aureus in a murine model of chronic peritoneal abscess. Intraperitoneal challenge with 3x108 CFUs of S. aureus (MRSA M2) in BALB/c mice resulted in 17% (n=2) mortality over 21 days in the vaccinated group and 92% (n=11) in the control group (Fig. 1) (p< 0.001). 80% (n=8) of the survived animals in the vaccinated group cleared the infection. Obtained results confirm the effectiveness of our pentavalent vaccine that targets both planktonic and biofilm-associated proteins in this specific model.en_US
dc.language.isoen_USen_US
dc.titleEvaluation of a Pentavalent Vaccine Against Staphylococcus aureus in a Murine Model of Chronic Peritoneal Abscessen_US
dc.typedissertationen_US
dc.contributor.advisorShirtliff, Mark
dc.description.urinameFull Texten_US
refterms.dateFOA2019-02-20T17:44:06Z


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