The broad goal ofthis proposed research is to determine the underlying molecular mechanisms required for S. aureus endocarditis vegetations to develop and to improve diagnosis of endocarditis by the use of state-of-the-art molecular imaging techniques. Acute bacterial endocarditis (ABE) is a potentially deadly disease caused by bacterial infection of heart valves. Coagulase-positive S. aureus infections are the leading cause of ABE and have the highest mortality rates, due to the increased incidence of antibiotic-resistance. 5. aureus expresses a unique non-proteolytic prothrombin (ProT) activator, staphylocoagulase that mediates recognition of fibrinogen by the active staphylocoagulase-ProT complex resulting in conversion of fibrinogen to fibrin. Fibrin generation is hypothesized to play a critical role in ABE pathology. During the K99 phase of my project, we developed novel active site-labeled ProT analogs that were use in Fluorescence Molecular Tomography (FMT) and Positron Emission Tomography fused with Computed Tomography (PETCT) studies to identify 5. aureus ABE, non-invasively in a mouse model ofthe disease. We discovered that staphylocoagulase not only activates ProT, but also localizes the staphylocoagulase- ProT complex to S. aureus vegetations by COOH-terminal interactions with Fragment D of fibrin/fibrinogen. Here, my newly established lab will use these imaging agents to assess whether staphylocoagualse is a virulence factor for 5. aureus in endocarditis. Furthermore, specific recognition of vegetations by our new endocarditis probes would aid in determining the role and importance of factor Xllla cross-linking to the pathology of endocarditis and facihtate identification of new adjunctive therapies targeting fibrin generation. Molecular imaging, biochemical, and immunology studies are proposed to test our hypotheses: that these SC is a virulence factor;that factor XIII activation stabilizes the fibrin network during ABE;and that new adjunctive therapies can limit vegetation grow in ABE.
Specific Aims are: (1) To determine whether staphylocoagulase is a virulence factor for S. aureus endocarditis (2) To determine whether S. aureus-induces activation of FXIII and fibrin cross-linking during ABE;and (3) To characterize the effect of argatroban and staphylocoagulase inhibitors on the vegetation development during ABE.

Public Health Relevance

Coagulase-positive Staphylococcus aureus infections account for 40-50% of neonatal ABE and 30-40% of ABE in adults between the ages of 16-60 years, with a mortality rate of 25-47%, even with antibiotic therapy Clinical imaging of ABE is performed by transesophageal echocardiography, which is often difficult to interpret due to poor image quality and variable bacterial attachment. New insight gained from the studies proposed here will also new avenues for design and validation on new bacterial specific imaging agents.

National Institute of Health (NIH)
National Heart, Lung, and Blood Institute (NHLBI)
Research Transition Award (R00)
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Special Emphasis Panel (NSS)
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Mcdonald, Cheryl
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Auburn University at Auburn
Schools of Pharmacy
Auburn University
United States
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Huang, Jiansheng; Smith, Forrest; Panizzi, Peter (2014) Ordered cleavage of myeloperoxidase ester bonds releases active site heme leading to inactivation of myeloperoxidase by benzoic acid hydrazide analogs. Arch Biochem Biophys 548:74-85
Panizzi, Peter; Stone, James R; Nahrendorf, Matthias (2014) Endocarditis and molecular imaging. J Nucl Cardiol 21:486-95