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Field of Research : Bacteriology
Socio-Economic Objective : Infectious Diseases
Australian State/Territory : VIC
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  • Researchers (14)
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  • Funded Activity

    ARC Future Fellowships - Grant ID: FT130100580

    Funder
    Australian Research Council
    Funding Amount
    $749,153.00
    Summary
    How Bacteria Fold Virulence Factors to Cause Disease. Bacteria use folding enzymes to assemble proteins essential for cell integrity and pathogenicity. These foldases include the Disulphide bridge proteins, which catalyse the introduction of disulfide bonds. This project will study two important human pathogens, Salmonella Typhimurium and uropathogenic Escherichia coli, to address the fundamental and poorly understood questions of diversity of Dsb networks across bacterial pathogens and the role .... How Bacteria Fold Virulence Factors to Cause Disease. Bacteria use folding enzymes to assemble proteins essential for cell integrity and pathogenicity. These foldases include the Disulphide bridge proteins, which catalyse the introduction of disulfide bonds. This project will study two important human pathogens, Salmonella Typhimurium and uropathogenic Escherichia coli, to address the fundamental and poorly understood questions of diversity of Dsb networks across bacterial pathogens and the role of these foldases in virulence. The research will reveal how bacterial virulence factors are folded, identify novel targets for therapeutic intervention and provide the basis for structure-based design on new antimicrobials in the future.
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    Funded Activity

    Linkage Projects - Grant ID: LP110200752

    Funder
    Australian Research Council
    Funding Amount
    $495,000.00
    Summary
    The development and evaluation of a new therapy for the prevention and treatment of bacterial infections in hospitals. The technology used in this project will enable products to be developed from the Australian dairy industry which may safely provide protection and treatment for diarrhoea acquired in hospitals for which there are few effective options. The product will be cost effective and can be used as a public health tool to control outbreaks in those most susceptible to severe disease.
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    Funded Activity

    Discovery Projects - Grant ID: DP180102987

    Funder
    Australian Research Council
    Funding Amount
    $477,446.00
    Summary
    How auto-transporter proteins mediate bacterial interactions. This project aims to investigate the structure-function relationships that underpin key auto-transporter roles in bacterial cell adhesion, aggregation and biofilm formation. Auto-transporter proteins are extremely common in bacteria where they play a central role in controlling bacterial interactions with other bacteria, with human cells, and with surfaces. This project will define the molecular mechanisms underlying these processes. .... How auto-transporter proteins mediate bacterial interactions. This project aims to investigate the structure-function relationships that underpin key auto-transporter roles in bacterial cell adhesion, aggregation and biofilm formation. Auto-transporter proteins are extremely common in bacteria where they play a central role in controlling bacterial interactions with other bacteria, with human cells, and with surfaces. This project will define the molecular mechanisms underlying these processes. This will have significant benefits, such as providing the basis for the development of approaches to block auto-transporter functions that contribute to the establishment of persistent and difficult to treat bacterial infections.
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    Funded Activity

    Discovery Projects - Grant ID: DP140101244

    Funder
    Australian Research Council
    Funding Amount
    $318,000.00
    Summary
    Investigation of a Novel Protein Implicated in Phosphate Metabolism in Bacteria. Phosphate is an important nutrient for all forms of life on Earth. A novel bacterial protein has been identified that appears to be important for the uptake or processing of phosphate, since mutants lacking the protein grow poorly inside certain cells of the human immune system (where phosphate levels are low) and in media containing low phosphate. The aims of this project are: to determine the role of the protein b .... Investigation of a Novel Protein Implicated in Phosphate Metabolism in Bacteria. Phosphate is an important nutrient for all forms of life on Earth. A novel bacterial protein has been identified that appears to be important for the uptake or processing of phosphate, since mutants lacking the protein grow poorly inside certain cells of the human immune system (where phosphate levels are low) and in media containing low phosphate. The aims of this project are: to determine the role of the protein by examining all phosphate containing molecules in our mutants; to determine its location in bacteria and functional domains; to identify other affected genes in our mutants; and, to find proteins that interact with this new protein. This project expects to demonstrate the importance of this protein in phosphate metabolism in bacteria.
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    Funded Activity

    Discovery Projects - Grant ID: DP150102287

    Funder
    Australian Research Council
    Funding Amount
    $333,400.00
    Summary
    Unraveling autotransporter function in bacterial aggregates and biofilms. Autotransporters are a large family of bacterial proteins that play a central role in pathogenesis. They promote the formation of cell clusters and biofilms, which are mechanisms for bacterial resistance to host immune factors and antibiotics. Currently, the precise mode of action of autotransporters is unknown. This project will examine the interplay between the structure and function of key autotransporter proteins. It .... Unraveling autotransporter function in bacterial aggregates and biofilms. Autotransporters are a large family of bacterial proteins that play a central role in pathogenesis. They promote the formation of cell clusters and biofilms, which are mechanisms for bacterial resistance to host immune factors and antibiotics. Currently, the precise mode of action of autotransporters is unknown. This project will examine the interplay between the structure and function of key autotransporter proteins. It is expected that the outcomes of this research will establish how these proteins mediate aggregation and biofilm formation. It may also provide three-dimensional structures of proteins that are strongly immunogenic and may represent targets for future vaccine design, as well as identify molecules that inhibit autotransporter function.
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    Funded Activity

    Linkage Infrastructure, Equipment And Facilities - Grant ID: LE150100035

    Funder
    Australian Research Council
    Funding Amount
    $610,000.00
    Summary
    A single molecule real-time DNA sequencing facility. A single molecule real-time DNA sequencing facility: A PacBio SMRT sequencing facility will be established and used to accelerate ten specific research programs across a breadth of biological disciplines at two institutions. A specialised high throughput DNA sequencing technology called Single Molecule Real-Time (SMRT) sequencing developed by Pacific Biosciences (PacBio) is revolutionising biological research. SMRT sequencing allows researche .... A single molecule real-time DNA sequencing facility. A single molecule real-time DNA sequencing facility: A PacBio SMRT sequencing facility will be established and used to accelerate ten specific research programs across a breadth of biological disciplines at two institutions. A specialised high throughput DNA sequencing technology called Single Molecule Real-Time (SMRT) sequencing developed by Pacific Biosciences (PacBio) is revolutionising biological research. SMRT sequencing allows researchers to discover important information in DNA and RNA molecules that are missed by other modern DNA sequencing approaches. It is expected that this facility will also be a key infrastructure resource for the wider scientific community, helping to address fundamental questions in biology.
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    Funded Activity

    Discovery Projects - Grant ID: DP120104911

    Funder
    Australian Research Council
    Funding Amount
    $270,000.00
    Summary
    Transport and innate immune properties of DNA in bacterial nano-sized vesicles. All types of living organisms release nano-sized membrane vesicles or “blebs” which they use for intercellular communication and transport of molecules. This project will determine how bacteria package DNA within these vesicles, how this DNA is transported into host cells and how it triggers immune responses in these cells.
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    Active Funded Activity

    Discovery Projects - Grant ID: DP210103881

    Funder
    Australian Research Council
    Funding Amount
    $429,700.00
    Summary
    Bacterial vesicles transport their bioactive cargo to the host nucleus. This project aims to investigate how bacterial membrane vesicles transport their cargo to the nucleus of cells and its impact on host cell functions. Bacteria use membrane vesicles as a means of communication with the host, but the full extent of their effects on host cells has yet to be fully elucidated. This project expects to generate new knowledge in the field using cutting-edge imaging and molecular biology approaches. .... Bacterial vesicles transport their bioactive cargo to the host nucleus. This project aims to investigate how bacterial membrane vesicles transport their cargo to the nucleus of cells and its impact on host cell functions. Bacteria use membrane vesicles as a means of communication with the host, but the full extent of their effects on host cells has yet to be fully elucidated. This project expects to generate new knowledge in the field using cutting-edge imaging and molecular biology approaches. The work should provide significant benefits, particularly towards the development of membrane vesicles in gene therapy, gene editing and other applications.
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    Funded Activity

    Discovery Projects - Grant ID: DP130102689

    Funder
    Australian Research Council
    Funding Amount
    $427,000.00
    Summary
    Biology and evolution of intracellular parasitism. This project will investigate the development of intracellular parasitism in environmental amoebae. The outcomes of this work will help to understand the mechanisms by which bacteria have evolved to survive inside cells and in some cases cause disease.
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    Showing 1-9 of 9 Funded Activites

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