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Research Topic : streptococcus pyogenes
Scheme : NHMRC Project Grants
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  • Funded Activity

    Characterising The Role Of Streptokinase Polymorphism In Invasive Pathogenesis Of Streptococcus Pyogenes.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $480,535.00
    Summary
    Invasive bacterial pathogens such as Streptococcus pyogenes, can hijack host proteins and use them to facilitate the disease process. S. pyogenes secrete streptokinase to activate a host protease (plasminogen) which is used by the bacterium to invade through host tissue. This project will characterise the molecular mechanisms involved in streptokinase mediated activation of plasminogen which will assist the generation of novel therapeutics to treat invasive diseases.
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    Funded Activity

    Investigation Of The Localisation, Transport And Vaccine Potential Of Group A Streptococcal Cell Surface Proteins.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $505,523.00
    Summary
    Streptococcus pyogenes (group A streptococcus; GAS) is a bacterium that causes human skin and throat infections as well as highly invasive diseases including necrotising fasciitis. Additionally, serious sequeale, including rheumatic fever and acute glomerulonephritis, may result following repeated infection. We have recently examined the GAS cell wall and identified 23 proteins that are surface exposed, 20 of which are novel. We hypothesise that a number of these surface exposed proteins represe .... Streptococcus pyogenes (group A streptococcus; GAS) is a bacterium that causes human skin and throat infections as well as highly invasive diseases including necrotising fasciitis. Additionally, serious sequeale, including rheumatic fever and acute glomerulonephritis, may result following repeated infection. We have recently examined the GAS cell wall and identified 23 proteins that are surface exposed, 20 of which are novel. We hypothesise that a number of these surface exposed proteins represent candidate vaccine antigens capable of conferring protective immunity. We therefore propose to examine these surface proteins as components of experimental vaccines against GAS.
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    Funded Activity

    Development Of Mucosal Anti-adhesive Vaccines Against Group A Streptococci

    Funder
    National Health and Medical Research Council
    Funding Amount
    $299,821.00
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    Funded Activity

    Cloning And Analysis Of Genes Encoding Pneumococcal Capsule Production

    Funder
    National Health and Medical Research Council
    Funding Amount
    $300,734.00
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    Funded Activity

    Molecular Analysis Of Pneumococcal Pathogenesis

    Funder
    National Health and Medical Research Council
    Funding Amount
    $396,516.00
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    Funded Activity

    Vaccines For Complex Organisms

    Funder
    National Health and Medical Research Council
    Funding Amount
    $53,855.00
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    Funded Activity

    How Bacterial Cell Surface Enzymes Contribute Towards D Isease Progression

    Funder
    National Health and Medical Research Council
    Funding Amount
    $161,897.00
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    Funded Activity

    How The Gene For A Surface Protein In Group A Streptoco Cci Is Targeted For Mutation

    Funder
    National Health and Medical Research Council
    Funding Amount
    $167,069.00
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    Funded Activity

    Mucosal Immunisation Against Respiratory Tract Pathogens

    Funder
    National Health and Medical Research Council
    Funding Amount
    $205,977.00
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    Funded Activity

    PrtFII, A Streptococcus Pyogenes Fibronectin Binding Protein, And Invasive Diseases.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $296,540.00
    Summary
    Our recent work revealed that, in the Aboriginal population, young age is a risk factor for severe invasive diseases caused by group A streptococcus. For group A streptococcus infection to occur, bacterial attachment is the first step. The bacterium attaches to host cells through interactions involving host fibronectin and the pathogen's fibronectin-binding proteins. We have found that streptococcal strains from severe disease cases are more likely to have the gene for PrtFII, a fibronectin bind .... Our recent work revealed that, in the Aboriginal population, young age is a risk factor for severe invasive diseases caused by group A streptococcus. For group A streptococcus infection to occur, bacterial attachment is the first step. The bacterium attaches to host cells through interactions involving host fibronectin and the pathogen's fibronectin-binding proteins. We have found that streptococcal strains from severe disease cases are more likely to have the gene for PrtFII, a fibronectin binding protein, than those from uncomplicated skin sores. In this application we propose to extend this observation and compare biochemical properties of PrtFII from strains belonging to the above two sets of collections. We hypothesise that PrtFII from invasive strains bind to fibronectin more tightly than the proteins from strains that cause uncomplicated infection. We also will test whether sera from invasive disease cases have lower titre of antibodies to the conserved region of PrtFII than sera from uncomplicated cases. A streptococcal vaccine by necessity has to be a multi-component vaccine to cover a wide spectrum of diseases and epidemiological differences. The study proposed here may provide a basis to argue whether or not to include PrtFII in such a multi-component vaccine.
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