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Research Topic : Proteomics
Field of Research : Medical Bacteriology
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Medical Bacteriology (9)
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  • Funded Activity

    The Identification Of Novel Diagnostics And Therapeutics From Bacterial Viruses Specific For The Foodborne Pathogen Campylobacter Jejuni Using Mass Spectrometry.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $313,788.00
    Summary
    Campylobacter jejuni is the leading cause of foodborne illness within Australia. To improve food safety there is a critical need for new therapeutics and diagnostics that target this agent. Within nature bacterial viruses possess proteins that can perform such a task. By using mass spectrometric analysis we aim to exploit billions of years of co-evolution to identify bacterial viral proteins that bind C. jejuni to identify novel means to limit and lower C. jejuni numbers in food sources.
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    Funded Activity

    The Role Of N-linked Protein Glycosylation In Campylobacter Jejuni Pathogenesis

    Funder
    National Health and Medical Research Council
    Funding Amount
    $757,600.00
    Summary
    Protein glycosylation is crucial in enabling C. jejuni to colonize poultry, which is the most common route to human infection. The roles played by this modification remain almost completely unknown yet are likely to be multi-factorial. This project will determine the function of glycosylation and thus lead to eventual interventions aimed at reducing the organism in poultry for human consumption.
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    Funded Activity

    A Proteomic Approach To The Identification Of Novel Virulence Factors In Neisseria Meningitidis And Neisseria Gonorrhoeae.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $234,502.00
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    Funded Activity

    Understanding The Role Of O-linked Glycosylation In Burkholderia Cenocepica For Host Survival Using Proteomic Approaches

    Funder
    National Health and Medical Research Council
    Funding Amount
    $222,004.00
    Summary
    The bacteria Burkholderia cenocepecia (Bc) is a common infection of Cystic Fibrosis suffers in Australia. ~20% CF patients infected with Bc will die due to lung failure. Due to this high death rate there is an urgent need to understand how Bc survives and causes disease in the host. This grant aims to understand how the attachment of sugars, a process known as glycosylation, affects the ability of Bc to survive in mammalian cells.
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    Funded Activity

    Discovery Projects - Grant ID: DP150104515

    Funder
    Australian Research Council
    Funding Amount
    $384,300.00
    Summary
    Bacterial poly-histidine triad proteins. The poly-histidine triad (Pht) proteins are a poorly characterised family of surface proteins expressed by the genus Streptococcus and other Gram-positive genera. Recent studies suggest an important role for Pht proteins in survival of these bacteria in low zinc (Zn) environments. The project hypothesis is that Pht proteins specifically recruit Zn from the extracellular environment and somehow make it available to ATP binding cassette (ABC) transport syst .... Bacterial poly-histidine triad proteins. The poly-histidine triad (Pht) proteins are a poorly characterised family of surface proteins expressed by the genus Streptococcus and other Gram-positive genera. Recent studies suggest an important role for Pht proteins in survival of these bacteria in low zinc (Zn) environments. The project hypothesis is that Pht proteins specifically recruit Zn from the extracellular environment and somehow make it available to ATP binding cassette (ABC) transport systems located in the bacterial plasma membrane, beneath the cell wall, facilitating Zn uptake by the bacterium. The aim of this project is to conduct comprehensive molecular characterization of the interactions between Pht proteins, Zn and ABC transporters, and the role of the histidine triad motifs in these interactions.
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    Funded Activity

    Understanding The Role Of The Essential Regulator WalKR In Staphylococcus Aureus

    Funder
    National Health and Medical Research Council
    Funding Amount
    $555,239.00
    Summary
    Staphylococcus aureus is one of the most common human bacterial pathogens. This project aims to characterise an important global control system in S. aureus, and determine if chemical inhibitors of this control system could be used to treat S. aureus disease in the future.
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    Funded Activity

    Glycosyltransferase Effectors Of Enteropathogenic E. Coli And Salmonella

    Funder
    National Health and Medical Research Council
    Funding Amount
    $320,891.00
    Summary
    This project aims to characterise the mechanisms of disease caused by bacterial pathogens including Salmonella and enteropathogenic E. coli. These pathogens cause a significant amount of diarrhoeal disease and mortality worldwide particularly in infants and in countries where water sanitation is poor. I aim to investigate the specific mechanisms the bacteria employ to manipulate and avoid our immune response during infection in order to better understand and combat diarrhoeal disease.
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    Funded Activity

    Mechanisms Of Antibiotic-induced Persistent Bacterial Infection

    Funder
    National Health and Medical Research Council
    Funding Amount
    $632,048.00
    Summary
    Golden staph still causes significant human infections and resistance to antibiotics is an ever growing problem with this bacteria. This project will determine how resistance to some antibiotics is also changing the bacteria to promote persistent, difficult to treat infections. The insights from this study will help understand evolution of this bacteria, and help design new strategies for management.
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    Funded Activity

    Identification Of Proteins Specific To Transmissible Pseudomonas Aeruginosa In Cystic Fibrosis Infection

    Funder
    National Health and Medical Research Council
    Funding Amount
    $443,007.00
    Summary
    Cystic fibrosis (CF) is the most common autosomal recessive disorder in humans, affecting 1:2000 people. Mortality is often caused by Pseudomonas aeruginosa lung infections which have recently been shown to occur not only environmentally but also via person-person contact, usually during CF clinic visits. This project will elucidate the molecular traits responsible for these 'epidemic' P. aeruginosa infections, with the aim of finding novel therapeutics and infection control strategies.
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    Showing 1-9 of 9 Funded Activites

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