CID 2950007 as an inhibitor of Staphylococcus aureus infections

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dc.contributor.advisor McDowell, Susan A.
dc.contributor.author England, Benjamin J.
dc.date.accessioned 2012-05-21T18:26:05Z
dc.date.available 2013-12-26T20:17:45Z
dc.date.created 2012-05-05
dc.date.issued 2012-05-05
dc.identifier.uri http://cardinalscholar.bsu.edu/handle/123456789/195888
dc.description.abstract Staphylococcus aureus (S. aureus) infections are deleterious to the body, sometimes leading to sepsis. Sepsis is a state of whole-body inflammation that occurs when a body begins fighting an infection. S. aureus is emerging as one of the more common sources of bacterial infection. Statins, a class of drugs meant to lower cholesterol, have had unexpected effects in the protection against S. aureus infections. However, concerns have been expressed over the depletion of mevalonate, which occurs with the use of statins. A compound called CID 2950007 has recently emerged as a possible adjunctive therapy for protection against S. aureus. CID 2950007 has a high specificity for binding to the GTPase CDC42, which plays a major role in S. aureus host cell invasion. Through several cytotoxicity assays, fluorescently-labeled bacteria, and western blot analysis, this research shows that CID 2950007 is non-toxic to cells and provides protection against S. aureus invasion.
dc.description.sponsorship Department of Biology
dc.subject.lcsh Rho GTPases -- Inhibitors.
dc.subject.lcsh Staphylococcus aureus infections -- Treatment.
dc.subject.lcsh Cell membranes -- Physiology.
dc.title CID 2950007 as an inhibitor of Staphylococcus aureus infections en_US
dc.description.degree Thesis (M.S.)
dc.date.liftdate 2012-05-22
dc.identifier.cardcat-url http://liblink.bsu.edu/catkey/1666987


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  • Master's Theses [5510]
    Master's theses submitted to the Graduate School by Ball State University master's degree candidates in partial fulfillment of degree requirements.

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