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Field of Research : Animal Protection (Pests And Pathogens)
Research Topic : Veterinary Virology
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Animal Protection (Pests And Pathogens) (16)
Microbiology (Excl. Virology) (8)
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  • Funded Activity

    Linkage Projects - Grant ID: LP0775052

    Funder
    Australian Research Council
    Funding Amount
    $75,354.00
    Summary
    Equine rhinitis A virus; molecular pathogenesis and methods for control. The horse industry in Australia is primarily based in rural locations and is a major contributor to the national economy both in terms of direct economic contribution to gross domestic product and as a major employer of people in regional Australia. The research proposed in this project will improve our understanding of the pathogenesis of a virus that causes respiratory disease in horses that is related to the virus that c .... Equine rhinitis A virus; molecular pathogenesis and methods for control. The horse industry in Australia is primarily based in rural locations and is a major contributor to the national economy both in terms of direct economic contribution to gross domestic product and as a major employer of people in regional Australia. The research proposed in this project will improve our understanding of the pathogenesis of a virus that causes respiratory disease in horses that is related to the virus that causes foot and mouth disease in ruminants and swine. The technology developed during this project would have a global market.
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    Funded Activity

    Discovery Projects - Grant ID: DP0665701

    Funder
    Australian Research Council
    Funding Amount
    $274,000.00
    Summary
    Blocking immune responses: a critical factor in herpesvirus virulence? The horse and poultry industries are two large, primarily rural based livestock production industries that are major contributors to the national economy. The research proposed in this project will improve our understanding of the pathogenesis of two important viral pathogens that are each a significant cost to their respective industry, and thus will ultimately reduce the cost of these two viruses to industry. In addition, .... Blocking immune responses: a critical factor in herpesvirus virulence? The horse and poultry industries are two large, primarily rural based livestock production industries that are major contributors to the national economy. The research proposed in this project will improve our understanding of the pathogenesis of two important viral pathogens that are each a significant cost to their respective industry, and thus will ultimately reduce the cost of these two viruses to industry. In addition, the technology developed during this project would have a global market and may be transferable to other viral pathogens of other domestic species.
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    Funded Activity

    Linkage Projects - Grant ID: LP0211604

    Funder
    Australian Research Council
    Funding Amount
    $394,345.00
    Summary
    Application of DNA vaccination to the control of gastrointestinal nematodes in livestock. Gastrointestinal nematode parasites inflict great losses in sheep and cattle and reliance on anthelmintic drugs for their control is problematic. Vaccination would provide a better alternative but has been difficult to achieve. This proposal aims to apply novel DNA vaccination strategies to the development of parasite vaccines through optimisation of DNA delivery, development of new vaccination vectors and .... Application of DNA vaccination to the control of gastrointestinal nematodes in livestock. Gastrointestinal nematode parasites inflict great losses in sheep and cattle and reliance on anthelmintic drugs for their control is problematic. Vaccination would provide a better alternative but has been difficult to achieve. This proposal aims to apply novel DNA vaccination strategies to the development of parasite vaccines through optimisation of DNA delivery, development of new vaccination vectors and modulation of immune responses by co-delivery of cytokine genes. The results of these studies will not only add a new approach to vaccine development against gastrointestinal parasites but will also contribute to our knowledge of DNA vaccination in large animals.
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    Funded Activity

    Linkage Projects - Grant ID: LP0561957

    Funder
    Australian Research Council
    Funding Amount
    $405,000.00
    Summary
    Application of in vivo electroporation to DNA immunisation. The in vivo delivery of plasmid DNA induces immune responses to the encoded protein vaccine. In large animals including humans, DNA vaccination needs to be further improved before becoming a commercial reality, at least partially due to the very low levels of expression in vivo. In vivo electroporation has proven to be an effective way to enhance the level of protein expression and increase DNA vaccine efficacy. We combine enhanced in .... Application of in vivo electroporation to DNA immunisation. The in vivo delivery of plasmid DNA induces immune responses to the encoded protein vaccine. In large animals including humans, DNA vaccination needs to be further improved before becoming a commercial reality, at least partially due to the very low levels of expression in vivo. In vivo electroporation has proven to be an effective way to enhance the level of protein expression and increase DNA vaccine efficacy. We combine enhanced in vivo expression using electroporation with the co-delivery of plasmids encoding cytokines to enhance and modulate DNA vaccine in sheep. We will apply our findings to bovine viral diarrhoea virus (BVDV), both as an animal model for humans and as an economically important diseases of livestock.
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    Funded Activity

    Linkage Projects - Grant ID: LP0776711

    Funder
    Australian Research Council
    Funding Amount
    $324,000.00
    Summary
    Defining domains within Mycoplasma hyopneumoniae surface proteins that interact with host extracellular matrix: efficacy testing of candidate vaccines in swine. Over 90% of Australian commercial pig production facilities are affected by Mycoplasma hyopneumoniae, the causative agent of swine enzootic pneumonia. This disease causes economic losses in Australia of over $20 million per annum and up to $1 billion per annum in major swine rearing countries worldwide. This project will determine the p .... Defining domains within Mycoplasma hyopneumoniae surface proteins that interact with host extracellular matrix: efficacy testing of candidate vaccines in swine. Over 90% of Australian commercial pig production facilities are affected by Mycoplasma hyopneumoniae, the causative agent of swine enzootic pneumonia. This disease causes economic losses in Australia of over $20 million per annum and up to $1 billion per annum in major swine rearing countries worldwide. This project will determine the protective efficacy of new generation vaccines against M. hyopneumoniae, which aim to block the colonisation process and prevent disease .
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    Funded Activity

    Linkage Projects - Grant ID: LP0455306

    Funder
    Australian Research Council
    Funding Amount
    $468,557.00
    Summary
    Identification and characterisation of Mycoplasma hyopneumoniae surface-molecules that interact with the host epithelium. Mycoplasma hyponeumoniae causes porcine enzootic pneumonia, a disease that significantly impacts swine production. Current vaccines are unable to prevent colonisation of the respiratory tract and are costly to produce and administer. The expression of microbial adhesins that mediate adherence to the extracellular matrix is considered the initial step in host colonisation for .... Identification and characterisation of Mycoplasma hyopneumoniae surface-molecules that interact with the host epithelium. Mycoplasma hyponeumoniae causes porcine enzootic pneumonia, a disease that significantly impacts swine production. Current vaccines are unable to prevent colonisation of the respiratory tract and are costly to produce and administer. The expression of microbial adhesins that mediate adherence to the extracellular matrix is considered the initial step in host colonisation for many bacterial pathogens. We propose to identify M. hyopneumoniae cell surface moleculaes that interact with components of the extracellular matrix. Targetting these cell surface molecules will lead to therapeutics that prevent disease and block colonisation, eventually eradicating the host pathogen from pig production facilities.
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    Funded Activity

    Linkage Projects - Grant ID: LP0989396

    Funder
    Australian Research Council
    Funding Amount
    $290,000.00
    Summary
    Determining the impact of protozoan pathogens and strongyle worms on prime lamb production. This research will benefit wool and prime lamb industries nation-wide as sheep scouring is prevalent in high-rainfall areas across Australia. Data generated from the project will be used to educate farmers and reduce the financial burden of sheep scouring. This project will also enhance Australia's reputation in the disease management sector and will result in reduced risk to public health due to a better .... Determining the impact of protozoan pathogens and strongyle worms on prime lamb production. This research will benefit wool and prime lamb industries nation-wide as sheep scouring is prevalent in high-rainfall areas across Australia. Data generated from the project will be used to educate farmers and reduce the financial burden of sheep scouring. This project will also enhance Australia's reputation in the disease management sector and will result in reduced risk to public health due to a better understanding and management of zoonotic parasite and microbacterial contamination of carcasses and water catchments.
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    Funded Activity

    Linkage Projects - Grant ID: LP0989620

    Funder
    Australian Research Council
    Funding Amount
    $420,000.00
    Summary
    Development of an attenuated vaccine to control the emerging bovine respiratory pathogen Mycoplasma bovis. The project will develop an attenuated vaccine to control the emerging bovine respiratory pathogen Mycoplasma bovis. This pathogen is a major contributor to bovine pneumonia in the feedlot industry and improved control will reduce reliance on antibiotics in cattle production.
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    Funded Activity

    Linkage Projects - Grant ID: LP0561961

    Funder
    Australian Research Council
    Funding Amount
    $225,000.00
    Summary
    Understanding the molecular basis of virulence in Brachyspira hyodysenteriae to improve vaccine design. Swine dysentery is a colonic infection of pigs caused by Brachyspira hyodysenteriae. The disease is widespread in Australia and causes great economic loss. An effective vaccine is not available. This study aims to identify factors associated with the bacterium's virulence, using comparative genomic and proteomic information. Virulence factors then will be targeted and tested as recombinant vac .... Understanding the molecular basis of virulence in Brachyspira hyodysenteriae to improve vaccine design. Swine dysentery is a colonic infection of pigs caused by Brachyspira hyodysenteriae. The disease is widespread in Australia and causes great economic loss. An effective vaccine is not available. This study aims to identify factors associated with the bacterium's virulence, using comparative genomic and proteomic information. Virulence factors then will be targeted and tested as recombinant vaccine candidates. This project will result in the development of an improved vaccine to control swine dysentery in rural Australia. Control of swine dysentery through vaccination will reduce antibiotic use on infected farms and improve the productivity and competitiveness of the Australian pig industry.
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    Funded Activity

    Linkage Projects - Grant ID: LP0454047

    Funder
    Australian Research Council
    Funding Amount
    $300,000.00
    Summary
    Proteomics and vaccine development in swine dysentery. Swine dysentery is an infectious disease of significant economic importance caused by Brachyspira hyodysenteriae. There is no effective vaccine available. This project will combine modern techniques in microbial genomics and proteomics to identify outer membrane proteins of B. hyodysenteriae and evaluate their role as candidate vaccine antigens.
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