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Current Selection
Scheme : Linkage Projects
Research Topic : VACCINES
Socio-Economic Objective : Biological sciences
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  • Funded Activity

    Linkage Projects - Grant ID: LP0218929

    Funder
    Australian Research Council
    Funding Amount
    $174,265.00
    Summary
    Novel vaccines and serotyping scheme for Haemophilus parasuis. Glasser's disease, caused by the bacterium Haemophilus parasuis, is a significant problem in Australian and overseas pig industries. Current approaches to the management of Glassers disease utilise antibacterials and also vaccines. However, antibacterials are of limited effectiveness in juvenile pigs (weaners) that are difficult to medicate other than by injection, and current vaccines are only protective against the serotypes incl .... Novel vaccines and serotyping scheme for Haemophilus parasuis. Glasser's disease, caused by the bacterium Haemophilus parasuis, is a significant problem in Australian and overseas pig industries. Current approaches to the management of Glassers disease utilise antibacterials and also vaccines. However, antibacterials are of limited effectiveness in juvenile pigs (weaners) that are difficult to medicate other than by injection, and current vaccines are only protective against the serotypes included in the vaccine. We propose to examine the immune response to natural infection and identify potential vaccine candidates which will then be tested in vaccine trials. The APAI will focus on developing a DNA-based typing scheme for H. parasuis.
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    Funded Activity

    Linkage Projects - Grant ID: LP0668358

    Funder
    Australian Research Council
    Funding Amount
    $90,000.00
    Summary
    Evaluation of the EG95 vaccine against hydatid infection in macropodid marsupials. A parasitic infection known as hydatids was introduced into Australia by Europeans and is now causing mortality in Australian wallabies and kangaroos, including amongst endangered species. A vaccine against the disease, that was developed in Australia for use in domestic livestock, is being evaluated to determine if it could be used to prevent hydatids closely monitored populations of endangered macropod marsupia .... Evaluation of the EG95 vaccine against hydatid infection in macropodid marsupials. A parasitic infection known as hydatids was introduced into Australia by Europeans and is now causing mortality in Australian wallabies and kangaroos, including amongst endangered species. A vaccine against the disease, that was developed in Australia for use in domestic livestock, is being evaluated to determine if it could be used to prevent hydatids closely monitored populations of endangered macropod marsupials, such as Petrogale penicillata.
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    Funded Activity

    Linkage Projects - Grant ID: LP0455647

    Funder
    Australian Research Council
    Funding Amount
    $389,025.00
    Summary
    Efficient organelle transformation. Chloroplasts and mitochondria are the powerhouses of plant and animal cells. Ability to express introduced genes in these organelles has enormous biotechnological potential in agriculture and medicine, but practical development has been almost stalled for 15 years by very low transformation efficiency. Plastid transformation is today routine only in tobacco; and mitochondrial transformation has been achieved only in yeasts and algae. We have developed a soluti .... Efficient organelle transformation. Chloroplasts and mitochondria are the powerhouses of plant and animal cells. Ability to express introduced genes in these organelles has enormous biotechnological potential in agriculture and medicine, but practical development has been almost stalled for 15 years by very low transformation efficiency. Plastid transformation is today routine only in tobacco; and mitochondrial transformation has been achieved only in yeasts and algae. We have developed a solution, and achieved the key technical requirements for proof of concept. This collaboration between industry, government and university partners will deliver key Australian-owned IP, for environmentally-friendly plant biofactories, and for treatment of mitochondrial genetic disorders.
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    Funded Activity

    Linkage Projects - Grant ID: LP0454145

    Funder
    Australian Research Council
    Funding Amount
    $405,000.00
    Summary
    The molecular basis for oocyst and cyst wall formation in apicomplexan parasites. Apicomplexan parasites such as Eimeria, Neospora, Toxoplasma and Plasmodium are single celled organisms - protozoa - that cause some of the most serious infectious diseases of livestock and humans ever known. Transmission of these parasites is dependent on their ability to encase themselves in protective structures known as oocyst or cyst walls. These walls are resistant to harsh environmental conditions, chemicals .... The molecular basis for oocyst and cyst wall formation in apicomplexan parasites. Apicomplexan parasites such as Eimeria, Neospora, Toxoplasma and Plasmodium are single celled organisms - protozoa - that cause some of the most serious infectious diseases of livestock and humans ever known. Transmission of these parasites is dependent on their ability to encase themselves in protective structures known as oocyst or cyst walls. These walls are resistant to harsh environmental conditions, chemicals and attack by the immune system. We will discover and characterise the molecular basis for cyst wall formation. This fundamental knowledge will be the building block for new, highly specific drugs and vaccines to control these extremely important pathogens.
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