Vaccination of poultry infected with multiple Salmonella serovars. Salmonella is a zoonotic, foodborne pathogen found on eggs and poultry meat. It is the second largest cause of human gastrointestinal disease, thus, reduction of Salmonella on poultry farms is paramount to public health. This project aims to evaluate the long-term efficacy of a commercial Salmonella Typhimurium vaccine against multiple serotypes, including the emerging Salmonella Enteritidis. This project will generate new knowle ....Vaccination of poultry infected with multiple Salmonella serovars. Salmonella is a zoonotic, foodborne pathogen found on eggs and poultry meat. It is the second largest cause of human gastrointestinal disease, thus, reduction of Salmonella on poultry farms is paramount to public health. This project aims to evaluate the long-term efficacy of a commercial Salmonella Typhimurium vaccine against multiple serotypes, including the emerging Salmonella Enteritidis. This project will generate new knowledge in avian immunology using an innovative approach to evaluate the host response to multi-serovar infection. Outcomes of this project will future proof the Australian poultry industry against exotic Salmonella serotypes benefitting the industry by significantly reducing risks of future outbreaks and economic loss.Read moreRead less
Biogenesis and functions of bacterial membrane vesicles. This project aims to investigate the mechanisms that regulate the production of bacterial membrane vesicles and how this determines their bacterial cargo and subsequent biological functions. Bacterial membrane vesicles are naturally produced nanoparticles released by all bacteria as part of their normal growth. These vesicles contain a range of bacterial cargo and function to promote bacterial survival and growth. This project will advance ....Biogenesis and functions of bacterial membrane vesicles. This project aims to investigate the mechanisms that regulate the production of bacterial membrane vesicles and how this determines their bacterial cargo and subsequent biological functions. Bacterial membrane vesicles are naturally produced nanoparticles released by all bacteria as part of their normal growth. These vesicles contain a range of bacterial cargo and function to promote bacterial survival and growth. This project will advance our knowledge regarding the regulation of bacterial membrane vesicle biogenesis, their composition and biological functions. Collectively, these findings will facilitate the development and refinement of membrane vesicle-based biotechnologies with broad applications.Read moreRead less
Discovery Early Career Researcher Award - Grant ID: DE200101524
Funder
Australian Research Council
Funding Amount
$355,325.00
Summary
Taking Control: Understanding regulation of bacterial iron acquisition. This project aims to uncover the bacterial regulatory networks acting on a family of iron-stealing molecules called siderophores. Bacteria use siderophores to acquire iron from their hosts, the environment, and each other – as such, they have a central role in microbial life. Despite their importance, we have an incomplete knowledge of how these iron-stealing weapons are deployed. This project will develop a new genomics-bas ....Taking Control: Understanding regulation of bacterial iron acquisition. This project aims to uncover the bacterial regulatory networks acting on a family of iron-stealing molecules called siderophores. Bacteria use siderophores to acquire iron from their hosts, the environment, and each other – as such, they have a central role in microbial life. Despite their importance, we have an incomplete knowledge of how these iron-stealing weapons are deployed. This project will develop a new genomics-based, high-throughput technology for defining bacterial gene regulation networks, and use it to understand siderophore control. This will provide new knowledge of siderophore function, enhance understanding of bacterial community and host interactions, and establish leadership in a new genomics technology in Australia.Read moreRead less
Dissecting bacterial signal transduction. Bacteria have feelings. They sense and respond to changes using proteins called two-component signalling systems (TCSS). These comprise a sensor which activates a DNA binding protein in response to specific cues (signals). Using state-of-the-art genetic techniques and a synthetic biology approach, this research aims to reveal for the first time how these complex bacterial TCSS networks interact. The outcomes will be a fundamental, new understanding of ho ....Dissecting bacterial signal transduction. Bacteria have feelings. They sense and respond to changes using proteins called two-component signalling systems (TCSS). These comprise a sensor which activates a DNA binding protein in response to specific cues (signals). Using state-of-the-art genetic techniques and a synthetic biology approach, this research aims to reveal for the first time how these complex bacterial TCSS networks interact. The outcomes will be a fundamental, new understanding of how bacteria sense and respond to environmental signals; a deep dive into how bacteria feel. This knowledge will be the basis for innovative approaches to harness bacteria in biotech such as vaccine production, biofuels, or clever therapeutic interventions to stop bacterial infections.Read moreRead less
Australian Laureate Fellowships - Grant ID: FL210100258
Funder
Australian Research Council
Funding Amount
$3,331,707.00
Summary
Understanding how bacteria adapt and function in the complex gut ecosystem. This project aims to investigate the role of the gut ecosystem in defining the structure and function of microbes. Given that one of the current challenges in microbiology is our inability to study individual microbes directly from complex, multi-microbial niches, this project aims to develop multidisciplinary methods to study microbes in their native state, to understand how they adapt to live in the gut. This understan ....Understanding how bacteria adapt and function in the complex gut ecosystem. This project aims to investigate the role of the gut ecosystem in defining the structure and function of microbes. Given that one of the current challenges in microbiology is our inability to study individual microbes directly from complex, multi-microbial niches, this project aims to develop multidisciplinary methods to study microbes in their native state, to understand how they adapt to live in the gut. This understanding should provide fundamental insights into adaptation mechanisms that lead to bacterial proliferation, disease and antibiotic resistance. As well as enhancing interdisciplinary collaborations, this work should provide economic benefits by contributing to improved gut health of animals, and more efficient food production.Read moreRead less
Discovery of Novel Bacteriophage with the Capacity to Modulate Gut Bacteria. This project aims to experimentally validate the largest ever collection of bacterial viruses (bacteriophages) within the gut microbiome. This project expects to generate new knowledge in the area of bacteriophage biology and genomics by using the innovative approaches of wet-lab and bioinformatic genome analyses. Expect outcomes of this project include the discovery of novel phages using bioinformatics, wet-lab validat ....Discovery of Novel Bacteriophage with the Capacity to Modulate Gut Bacteria. This project aims to experimentally validate the largest ever collection of bacterial viruses (bacteriophages) within the gut microbiome. This project expects to generate new knowledge in the area of bacteriophage biology and genomics by using the innovative approaches of wet-lab and bioinformatic genome analyses. Expect outcomes of this project include the discovery of novel phages using bioinformatics, wet-lab validation of their activity and characterisation of their potential to contribute new bacterial host metabolism. This should provide benefits, such as advancement to our understanding of bacteriophages, improved bioinformatic software, and a characterised collection of commercially valuable bacterial strains and phages.Read moreRead less
Hitting bacteria with a Bam: Lectin-Like Antimicrobials as New Antibiotics. Antibiotic resistance in disease-causing bacteria is a rapidly growing problem, making the development of new antibiotics of critical importance. This project aims to develop naturally produced lectin-like protein antibiotics as novel antimicrobial agents. To achieve this, the project will produce an extensive library of these antibiotics and test them for potency and specificity. Using cutting-edge techniques, it will d ....Hitting bacteria with a Bam: Lectin-Like Antimicrobials as New Antibiotics. Antibiotic resistance in disease-causing bacteria is a rapidly growing problem, making the development of new antibiotics of critical importance. This project aims to develop naturally produced lectin-like protein antibiotics as novel antimicrobial agents. To achieve this, the project will produce an extensive library of these antibiotics and test them for potency and specificity. Using cutting-edge techniques, it will determine how these antibiotics kill cells on a molecular and cellular level. It is anticipated this research will create the tools and knowledge required to exploit lectin-like protein antibiotics to fight bacterial infection, which will lead to their use in the prevention of crop and livestock losses due to disease.Read moreRead less
Antigen selection mechanisms control T cell immunity against bacteria. CD4+ T (T helper) cells are required to control many important bacterial infections. This Project aims to identify the key targets of CD4+ T cells responding to a model bacterial infection, and to correlate potential antigen effectiveness with native expression, antigen presentation, and the function of antigen-specific CD4+ T cells over time. Our validated experimental 'pipeline' has unprecedented potential to define potent ....Antigen selection mechanisms control T cell immunity against bacteria. CD4+ T (T helper) cells are required to control many important bacterial infections. This Project aims to identify the key targets of CD4+ T cells responding to a model bacterial infection, and to correlate potential antigen effectiveness with native expression, antigen presentation, and the function of antigen-specific CD4+ T cells over time. Our validated experimental 'pipeline' has unprecedented potential to define potent CD4+ T cell antigens within the thousands of proteins expressed by a bacterial pathogen. Our unbiased analysis may help establish the rules that define effective antigenicity. Our work will improve the understanding of bacterial immunity, and inform future design of T-cell based vaccines in the agricultural sector.Read moreRead less
Mechanism of secretion of large clostridial toxins . This project aims to investigate how the large clostridial toxins are secreted from important animal bacterial pathogens. This project expects to generate new knowledge about how bacteria interact with hosts through protein secretion, using a collaborative and interdisciplinary approach and cutting-edge techniques. Expected outcomes of this project include building a deep understanding of the role of export machinery in toxin secretion from ba ....Mechanism of secretion of large clostridial toxins . This project aims to investigate how the large clostridial toxins are secreted from important animal bacterial pathogens. This project expects to generate new knowledge about how bacteria interact with hosts through protein secretion, using a collaborative and interdisciplinary approach and cutting-edge techniques. Expected outcomes of this project include building a deep understanding of the role of export machinery in toxin secretion from bacteria, and the identification of new systems by which this is achieved. This should provide significant benefits, such as gaining new insights into new bacterial protein export mechanisms, with the aim of identifying targets for future veterinary disease interventions or biotechnological applications.Read moreRead less
Manipulation of mitochondrial function by Legionella pneumophila. . The intracellular bacterial pathogen Legionella pneumophila co-evolved with eukaryotic hosts and has developed sophisticated mechanisms to manipulate human cell function – mitochondria in particular – by secreting >300 effector proteins through a specialised Type-IV system into the host cell. This research aims to understand the function of effector proteins targeted to mitochondria; delivering important new knowledge in host-pa ....Manipulation of mitochondrial function by Legionella pneumophila. . The intracellular bacterial pathogen Legionella pneumophila co-evolved with eukaryotic hosts and has developed sophisticated mechanisms to manipulate human cell function – mitochondria in particular – by secreting >300 effector proteins through a specialised Type-IV system into the host cell. This research aims to understand the function of effector proteins targeted to mitochondria; delivering important new knowledge in host-pathogen and mitochondrial biology and advanced cell biology tools. With most of the effector proteins yet to be characterised, benefits from the project will be to reveal specifically how these target mitochondria, and more broadly, how bacterial pathogens manipulate organelles for their survival.Read moreRead less