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Research Topic : Staphylococcus
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  • Funded Activity

    Predictors Of Treatment Outcome In Staphylococcus Aureus Bacteraemia: A Multi-centre Analysis In Australasia.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $147,952.00
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    Funded Activity

    The Epidemiology Of Staphylococcus Aureus And Antibiotic Resistance In Community-acquired Infections

    Funder
    National Health and Medical Research Council
    Funding Amount
    $1,267,784.00
    Summary
    Staphylococcus aureus infections range from boils to life-threatening diseases and are increasingly resistant to antibiotics and difficult to treat. This study follows patients with community-acquired S. aureus infections, and close contacts, for 24 months to see if they carry S. aureus (nose swabs) or develop infection. Our data on risk factors for colonisation and infection will help doctors decide whether to trace and treat contacts of patients to protect households from further infection.
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    Funded Activity

    Characterisation Of The Host Response In A Mouse Model Of Staphylococcus Aureus Keratitis.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $248,850.00
    Summary
    Staphylococcus is the most common cause of bacterial eye infections (microbial keratitis) . This ocular infection is associated with severe pain, redness, discharge and frequently results in the loss of vision or blindness. Predisposing factors for this disease include contact lens wear and immunocompromised individuals such as those with HIV, diabetes or aged populations. S. aureus keratitis is difficult to treat using conventional antibiotics as although bacteria may be eliminated, vision loss .... Staphylococcus is the most common cause of bacterial eye infections (microbial keratitis) . This ocular infection is associated with severe pain, redness, discharge and frequently results in the loss of vision or blindness. Predisposing factors for this disease include contact lens wear and immunocompromised individuals such as those with HIV, diabetes or aged populations. S. aureus keratitis is difficult to treat using conventional antibiotics as although bacteria may be eliminated, vision loss may still result from scarring. S. aureus also causes a wide range of hospital associated infections such as pneumonia, endocarditis, bacteremia, wound infections, osteomyelitis and septic arthritis. In recent times strains of S. aureus have emerged which are multi-drug resistant including methicillin resistant S. aureus (MRSA). These may only be treated with the drug Vancomycin. However, vancomycin resistant S. aureus have been reported in both Japan and the USA. Now, the search for new treatments for this bacterium is of vital importance. This project will utilise the novel S.aureus mouse model for keratitis, which we have developed in our laboratories. Our model will enable us to investigate the host responses to bacterial infection. Existing models in the rabbit do not allow such detailed studies due to the lack of existing molecular probes and antibodies. Insights into potential adjunct therapies will also be gained. This research could lead to the development of novel therapeutic measures aimed at manipulating the host response to reduce scarring and consequent blindness. This information may also be important for the development of prophylactic treatments for those patients at high risk, such as diabetics and immunocompromised individuals of developing this disease.
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    Funded Activity

    Improving Clinical Outcomes Of Antimicrobial Resistant Infections With A Drug-free Intervention

    Funder
    National Health and Medical Research Council
    Funding Amount
    $999,581.00
    Summary
    Superbugs, or antimicrobial-resistant pathogens, cause recurring infections and non-healing wounds after surgery as existing therapies fail to effectively kill them. We will develop a medical device to fight superbugs with UV light that is effective against bacteria and fungi without causing harm to human cells. This could eradicate superbugs at infection sites, aid wound healing and actively improve health outcomes after surgery.
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    Funded Activity

    Evaluating Hand Hygiene Interventions And Their Ability To Reduce Haelthcare Associated Infection

    Funder
    National Health and Medical Research Council
    Funding Amount
    $508,848.00
    Summary
    Healthcare associated infection is a major problem for Australian hospitals. One of the best ways to reduce it is to improve hand hygiene among hospital workers. The National Hand Hygiene Initiative (NHHI) is currently being implemented to improve hygiene among health care workers. This research will evaluate the NHHI and measure how well the program works, what factors are important to its success, and whether implementing the program is good value for money.
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    Funded Activity

    Molecular Mechanisms Of Low-level Vancomycin Resistance In Clinical Staphylococcus Aureus

    Funder
    National Health and Medical Research Council
    Funding Amount
    $437,916.00
    Summary
    The common bacteria Staphylococcus aureus causes many infections in humans, and is becoming more resistant to antibiotic treatments, especially in hospitals. This project will determine how this bacteria is developing resistance to some of our last available antibiotics. This will provide an important basis for detecting and preventing this antibiotic resistance problem in future.
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    Funded Activity

    Characterisation Of Community Methicillin-resistant Staphylococcus Aureus And Their Control In Remote Communities

    Funder
    National Health and Medical Research Council
    Funding Amount
    $300,777.00
    Summary
    Before the introduction of antibiotics Staphylococcus aureus, the golden staph , was the major cause of infections in hospitals. Although the introduction of antibiotics helped control the organism it has gradually acquired resistance until strains have emerged which can only be treated with vancomycin. Consequently staphs have again emerged as a major hospital pathogen. The emergence of these multiply resistant strains corresponded to them acquiring methicillin resistance and consequently they .... Before the introduction of antibiotics Staphylococcus aureus, the golden staph , was the major cause of infections in hospitals. Although the introduction of antibiotics helped control the organism it has gradually acquired resistance until strains have emerged which can only be treated with vancomycin. Consequently staphs have again emerged as a major hospital pathogen. The emergence of these multiply resistant strains corresponded to them acquiring methicillin resistance and consequently they have come to be known as methicillin-resistant Staphylococcus aureus or MRSA. Soon after the emergence of MRSA the hospitals of Western Australia (WA) developed a policy to prevent introduced MRSA from becoming established in its hospitals. Although this has been successful the policy is now under threat with the emergence of MRSA in remote WA Aboriginal communities. Aboriginals in these communities have a large number of infections which are usually treated empirically. This can result in the selection of antibiotic resistant bacteria if they are present. Consequently, it is planned to regularly screen Aboriginal communities which are known to have a high prevalence of MRSA and recommend antibiotic prescribing which will not select for any resistant staphylococci carried by a person. This is possible because the community MRSA are still susceptible to some anti-staphylococcal drugs. If this program is shown to reduce the prevalence of MRSA in the communities then the program will be extended to other communities. Community MRSA are now being reported from other Australian states and it is planned to study these to see if they are related to the WA strains. The community isolates will be studied to assess their potential to acquire additional antibiotic resistances. As some strains are known to be more of a threat to hospitals than others methods will be investigated to develop rapid methods for detecting them.
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    Funded Activity

    Understanding Virulence Of Invasive Staphylococcus Aureus

    Funder
    National Health and Medical Research Council
    Funding Amount
    $772,711.00
    Summary
    Staph aureus (Golden staph) is a major cause of disease in humans. In this project we will use state-of-the-art molecular biology and genomics to fully understand the mechanisms of virulence in this pathogen. This information will inform future approaches to development of therapeutics, as well as the use of genomics in clinical microbiology and disease management.
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    Funded Activity

    Applying Pharmacometrics To Develop Novel Treatment Strategies For Staphylococcus Aureus Infections In Children

    Funder
    National Health and Medical Research Council
    Funding Amount
    $368,562.00
    Summary
    My research will determine the best way to give antibiotics to treat Staphylococcus aureus, one of the most common causes of infection in children. This includes finding out if we can provide highly effective treatment with antibiotics given by mouth instead of through a drip, and with fewer doses each day, so we can treat kids at home instead of in hospital. I will also explore new ways to use common antibiotics to treat antibiotic-resistant infections.
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    Funded Activity

    CAMERA: Combination Antibiotic Treatment For Methicillin Resistant Staphylococcus Aureus Bacteraemia - A Randomised Controlled Trial

    Funder
    National Health and Medical Research Council
    Funding Amount
    $1,162,248.00
    Summary
    MRSA (golden staph) is resistant to the most useful class of antibiotics: beta-lactams. It is more difficult to treat than antibiotic-sensitive strains. Standard treatment for MRSA is vancomycin but it has high failure rates. Although MRSA is resistant to beta-lactams, lab studies show that they enhance vancomycin’s bacterial killing when used together. CAMERA2 is an RCT comparing vancomycin alone to combination therapy (vancomycin plus flucloxacillin) for adults with MRSA blood stream infection
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