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Scheme : NHMRC Project Grants
Research Topic : Virus evolution
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  • Funded Activity

    Macrophages Drives The Diversity Of HIV

    Funder
    National Health and Medical Research Council
    Funding Amount
    $654,381.00
    Summary
    The diversity of HIV quasispecies within a single AIDS patient is far greater than the global diversity of influeneza annually, highlighting the enormous burden HIV imposes on the immune network. The capacity of HIV-1 to evolve quickly has significantly impaired our effort to produce effective vaccine and long lasting treatment strategy. This project utilizes multidisciplinary approaches to delineate determinants that drives the diversification of HIV-1.
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    Funded Activity

    Understanding The Likely Population Impact Of New And Improved Influenza Vaccines

    Funder
    National Health and Medical Research Council
    Funding Amount
    $358,678.00
    Summary
    Influenza causes a large burden of death and disease each year, as well as disruptive pandemics. Vaccines that could protect against more than one season�s flu strains (including new pandemic viruses) would be highly desirable, and may be on the horizon. Our aim is to understand the likely impact of these new vaccines on the way flu viruses spread between people, and change from one season to the next. This information is needed to justify their introduction, and inform their best use.
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    Funded Activity

    Replication And Pathogenesis Of DHBV

    Funder
    National Health and Medical Research Council
    Funding Amount
    $378,604.00
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    Funded Activity

    Molecular Studies On Mosquito-borne Viruses

    Funder
    National Health and Medical Research Council
    Funding Amount
    $318,153.00
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    Funded Activity

    Growth Of Hepatitis C Virus

    Funder
    National Health and Medical Research Council
    Funding Amount
    $369,941.00
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    Funded Activity

    Factors Affecting The Outcome Of Hepatitis B-like Infec Tions

    Funder
    National Health and Medical Research Council
    Funding Amount
    $146,336.00
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    Funded Activity

    Structure And Function Of The HCV Glycoproteins

    Funder
    National Health and Medical Research Council
    Funding Amount
    $598,863.00
    Summary
    Hepatitis C Virus infects 3% of the world's population causing recurring liver disease, cirrhosis and hepatocellular carcinoma. To infect a liver cell, the viral glycoproteins attach to cell surface molecules wher they are activated to mediate merger of the viral and cellular membranes. This project grant will explore how the viral glycopropteins become activated and obtain essential structural information on the viral glycoproteins. These studies will help us to design antiviral agents.
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    Funded Activity

    Viral Infection And Exacerbations Of Asthma During Pregnancy: Characteristics, Mechanisms And Consequences

    Funder
    National Health and Medical Research Council
    Funding Amount
    $465,210.00
    Summary
    At least 12% of pregnant women in Australia have asthma and more than half of these women will experience an acute attack during pregnancy. This puts the fetus at risk of poor outcomes such as low birth weight or premature birth, which has a significant impact on their health in both the short term and long term. The mechanisms which lead to exacerbations of asthma during pregnancy are unknown, but have implications for the treatment of pregnant women with asthma. In non-pregnant adults, the maj .... At least 12% of pregnant women in Australia have asthma and more than half of these women will experience an acute attack during pregnancy. This puts the fetus at risk of poor outcomes such as low birth weight or premature birth, which has a significant impact on their health in both the short term and long term. The mechanisms which lead to exacerbations of asthma during pregnancy are unknown, but have implications for the treatment of pregnant women with asthma. In non-pregnant adults, the majority of asthma exacerbations are caused by viral infection and it is likely that a similar mechanism operates in pregnant women with asthma. No previous studies have identified the viruses responsible for exacerbations of asthma during pregnancy. We currently have a promising lead in this area, with data showing that one third of pregnant women with asthma have a severe exacerbation of their asthma requiring medical intervention during pregnancy, and a large proportion of these are likely to be due to viral infection. We propose that during pregnancy, pregnant women with asthma are more susceptible to viral infection than pregnant women without asthma. We also suggest that women with asthma will have more severe viral infections during pregnancy, and that these will contribute to the majority of acute asthma attacks during pregnancy. This project will determine the rate of infection among pregnant women with and without asthma and determine the viruses responsible for acute attacks of asthma during pregnancy. The study will also explore the inflammatory mechanisms which predispose women to viral infection. These results will contribute to a greater understanding of the mechanisms leading to exacerbations of asthma during pregnancy and will be used to develop more appropriate asthma monitoring and treatment strategies for pregnant women, which will have health benefits for both mother and baby.
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    Funded Activity

    Viral Factors Involved In Flavivirus Replication And Virus-host Interactions

    Funder
    National Health and Medical Research Council
    Funding Amount
    $743,696.00
    Summary
    With our increased understanding of virus-host interactions it has become apparent that small, non-structural proteins and small RNAs of most viruses are vital for numerous, often multiple, functions in the viral life cycle. In the proposed project, we seek to gain a detailed understanding of the functions of small nonstructural protein NS2A and small abundant viral RNAs of medicaly important encephalitic flaviviruses, which have remained so far elusive and are at the cutting-edge in the researc .... With our increased understanding of virus-host interactions it has become apparent that small, non-structural proteins and small RNAs of most viruses are vital for numerous, often multiple, functions in the viral life cycle. In the proposed project, we seek to gain a detailed understanding of the functions of small nonstructural protein NS2A and small abundant viral RNAs of medicaly important encephalitic flaviviruses, which have remained so far elusive and are at the cutting-edge in the research field. We anticipate that with a better understanding of the roles of these factors in flaviviral replication and pathogenesis, novel targets for antiviral therapies and-or molecular determinants for inclusion in candidate vaccines will be identified.
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    Funded Activity

    Structure And Function Of Hepatitis C Virus Glycoproteins

    Funder
    National Health and Medical Research Council
    Funding Amount
    $480,750.00
    Summary
    Hepatitis C Virus infects approximately 200 million people world-wide and is the major cause of liver transplantation in the Western world. At present there is no vaccine and interferon alpha is the only therapy available and has only limited success in clearing viral infection. HCV is distantly related to flaviviruses eg tick-borne encephaltitis virus and yellow fever virus. All viruses attach to target cells using receptors to initiate the infection process. In the case of HCV, the envelope gl .... Hepatitis C Virus infects approximately 200 million people world-wide and is the major cause of liver transplantation in the Western world. At present there is no vaccine and interferon alpha is the only therapy available and has only limited success in clearing viral infection. HCV is distantly related to flaviviruses eg tick-borne encephaltitis virus and yellow fever virus. All viruses attach to target cells using receptors to initiate the infection process. In the case of HCV, the envelope glycoproteins interact with as yet unknown receptors on the target cell surface resulting in the virus being internalized into endosomes. It is believed that the low pH environment of these endosomes triggers fusion of the viral and cellular membranes. After fusion the genome of the virus is released into target cells and begins the replication process. The actual events intitiating these processes are not understood for HCV but are believed to be mediated using two envelope glycoproteins. In this project we seek to gain a greater understanding of how viral fusion and entry occurs. We have new information regarding the localisation of the two envelope glycoproteins that will now enable us to carefully examine how viral fusion occurs. Using biochemical approaches, we will study their structure and function and examine how this relates to the well understood flavivirus mode of fusion and entry. We will test the functional consequences of altering the structure of the HCV envelope glycoproteins by developing in vitro assays of HCV fusion. Assays for HCV fusion are essential for future studies to identify viral receptors, examine the role of antibody in viral neutralization and can be used to test novel inhibitors of viral fusion and entry.
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