Unlocking the potential of bacterial polymers by defining key determinants. Sugary structures that coat the surface of some bacteria, known as capsules, can be modified by bacterial viruses (bacteriophage) in the environment. For the bacterial genus Acinetobacter, this influences their use as naturally renewable 'green' biopolymers for remediating environments contaminated with petroleum hydrocarbons. This project aims to characterise crucial capsule polymerase enzymes using a combination of bio ....Unlocking the potential of bacterial polymers by defining key determinants. Sugary structures that coat the surface of some bacteria, known as capsules, can be modified by bacterial viruses (bacteriophage) in the environment. For the bacterial genus Acinetobacter, this influences their use as naturally renewable 'green' biopolymers for remediating environments contaminated with petroleum hydrocarbons. This project aims to characterise crucial capsule polymerase enzymes using a combination of bioinformatics and experimental methodologies to establish how bacteriophage influence Acinetobacter capsules. Outcomes include the development of an innovative genomics pipeline to detect capsule change, improving the use of living bacteria for bioremediation and sustainable rehabilitation of natural ecosystems.Read moreRead less
Discovery Early Career Researcher Award - Grant ID: DE240100316
Funder
Australian Research Council
Funding Amount
$435,431.00
Summary
Population genomic methods for modelling bacterial pathogen evolution. This project aims to develop novel techniques to model bacterial genome evolution and improve our understanding of how major agricultural and human pathogens, including Enterococcus, Salmonella and E. coli, evolve. The project expects to generate new knowledge about how horizontal gene transfer shapes the evolution of bacteria and how these dynamics vary over different temporal scales. Expected outcomes include methodological ....Population genomic methods for modelling bacterial pathogen evolution. This project aims to develop novel techniques to model bacterial genome evolution and improve our understanding of how major agricultural and human pathogens, including Enterococcus, Salmonella and E. coli, evolve. The project expects to generate new knowledge about how horizontal gene transfer shapes the evolution of bacteria and how these dynamics vary over different temporal scales. Expected outcomes include methodological advances that will enable the analysis of massive contemporary datasets. These methods and resulting analyses will provide significant benefits including informing the design of superior long-term interventions to reduce bacterial disease in both agriculture and health that are robust to the evolution of bacteria.Read moreRead less
Data-led bioengineering to uncover hidden chemical wealth in bacteria. The soil bacteria Nocardia are an untapped source of industrially prized chemical compounds called natural products. This project aims to develop innovative bioprospecting genomics technologies built from the disciplines of microbiology, biochemistry and computational statistics to discover hundreds of new natural products in Nocardia. This project will unlock the diversity of potent new enzymes and molecules with high econom ....Data-led bioengineering to uncover hidden chemical wealth in bacteria. The soil bacteria Nocardia are an untapped source of industrially prized chemical compounds called natural products. This project aims to develop innovative bioprospecting genomics technologies built from the disciplines of microbiology, biochemistry and computational statistics to discover hundreds of new natural products in Nocardia. This project will unlock the diversity of potent new enzymes and molecules with high economic value that could include insecticides to protect crops, bioactives to fight diseases, or new enzymes for food and biofuel production. This research unlocks enormous hidden chemical potential in soil bacteria, to build sustainable national economic growth through innovative, high-value industrial chemical development.Read moreRead less
Discovery Early Career Researcher Award - Grant ID: DE120101730
Funder
Australian Research Council
Funding Amount
$375,000.00
Summary
Targeting cell death pathways in parasites. Schistosomiasis is a disease caused by parasitic worms. Due to the potential for drug resistance, new drugs are needed. This project aims to identify the components needed for parasite survival based on a cell death pathway in schistosomes. Neutralising the activities of these proteins should cause parasite death, providing a new treatment strategy.
Evolution of diverse symbiotic phenotypes among native soil bacteria following spread of a genomic island from a rhizobial inoculant. The quality of legume protein depends on symbiotic nitrogen fixation by root nodule bacteria (RNB). Sustainable legume production in Australian agriculture depends on legume inoculation with effective strains of these bacteria. Unfortunately inoculant strains transfer DNA to other soil bacteria resulting in soil populations of RNB that compete for nodulation but a ....Evolution of diverse symbiotic phenotypes among native soil bacteria following spread of a genomic island from a rhizobial inoculant. The quality of legume protein depends on symbiotic nitrogen fixation by root nodule bacteria (RNB). Sustainable legume production in Australian agriculture depends on legume inoculation with effective strains of these bacteria. Unfortunately inoculant strains transfer DNA to other soil bacteria resulting in soil populations of RNB that compete for nodulation but are less effective in nitrogen fixation. This transfer of DNA threatens a $2 billion asset in Australian agriculture. We will use molecular microbial ecology to investigate the mechanisms of genetic transfer of symbiotic DNA in RNB, and use this knowledge to prevent it.Read moreRead less
Understanding an exotic disease: Initiation of sex and infection by the sugarcane smut Ustilago scitaminea. Australian sugar exports generate almost $2 billion in annual sales, making the sugar industry a critical facet of the Australian economy. In 2006, Australia's primary sugar producing region came under threat when an outbreak of sugarcane smut caused by the fungus Ustilago scitaminea first appeared in Queensland. Management of this potentially devastating disease has focused on breeding pr ....Understanding an exotic disease: Initiation of sex and infection by the sugarcane smut Ustilago scitaminea. Australian sugar exports generate almost $2 billion in annual sales, making the sugar industry a critical facet of the Australian economy. In 2006, Australia's primary sugar producing region came under threat when an outbreak of sugarcane smut caused by the fungus Ustilago scitaminea first appeared in Queensland. Management of this potentially devastating disease has focused on breeding programmes aimed at developing resistant sugarcane cultivars, a complex process hampered by a lack of information about the mechanisms of smut resistance. Our research will provide key insight into the mechanisms by which U. scitaminea infects sugarcane, directing future breeding efforts and protecting this valuable industry against further outbreaks.Read moreRead less
Bacterial Proteomics: From Cell Division to Novel Antibiotic Targets. When a cell divides it is essential that each newborn cell gets a complete copy of the DNA. To ensure that this happens, cell division must be tightly controlled. It is not known how this occurs in bacteria. However, if we knew what molecules were involved in this control, we could target them to kill harmful bacteria. This project aims to identify such regulatory molecules as candidate targets for antimicrobial agents, with a ....Bacterial Proteomics: From Cell Division to Novel Antibiotic Targets. When a cell divides it is essential that each newborn cell gets a complete copy of the DNA. To ensure that this happens, cell division must be tightly controlled. It is not known how this occurs in bacteria. However, if we knew what molecules were involved in this control, we could target them to kill harmful bacteria. This project aims to identify such regulatory molecules as candidate targets for antimicrobial agents, with a view to developing powerful, novel antibiotics to protect us from the imminent threat of bioterrorism and antibiotic-resistant bacteria.
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The effect of age on regulatory T cell control of the innate and adaptive antiviral immune responses. Viral pathogens are a lead cause of infant mortality in the world. This project will define how T regulatory cells limit protective antiviral immune responses in the young. This information is critical for the development of potent antiviral vaccines that are effective from the newborn period without inducing autoimmunity. It will also provide novel insight into the way T regulatory cells can b ....The effect of age on regulatory T cell control of the innate and adaptive antiviral immune responses. Viral pathogens are a lead cause of infant mortality in the world. This project will define how T regulatory cells limit protective antiviral immune responses in the young. This information is critical for the development of potent antiviral vaccines that are effective from the newborn period without inducing autoimmunity. It will also provide novel insight into the way T regulatory cells can be manipulated both to dampen immunity, which can be used to develop strategies to reduce immune mediated disease and limit transplant rejection. Read moreRead less
Novel link between bacterial sugar metabolism and cell-to-cell signalling. This project aims to understand the role and function of the bacterial communication system that enables bacteria to form complex communities and alter phenotypic traits, essential for survival in their environment. Bacteria survive in their environmental niches by developing complex multicellular communities. Cell to cell communication, termed quorum sensing (QS), is critical for this process and is linked to their capac ....Novel link between bacterial sugar metabolism and cell-to-cell signalling. This project aims to understand the role and function of the bacterial communication system that enables bacteria to form complex communities and alter phenotypic traits, essential for survival in their environment. Bacteria survive in their environmental niches by developing complex multicellular communities. Cell to cell communication, termed quorum sensing (QS), is critical for this process and is linked to their capacity to detect and secrete small signalling molecules, autoinducers. This project will provide a new paradigm in bacterial adaptation through comprehensive characterisation of the Autoinducer-2 QS system. This knowledge will provide future opportunities for intervention in microbial infestation with broad potential benefits.Read moreRead less
The role of central carbon metabolism in cell cycle control in bacteria. Bacteria are simple organisms, yet we still do not understand how they coordinate their growth with their reproduction so faithfully, generation after generation, to produce viable newborn cells. The new discovery of a link between the food bacteria eat and the first stage of their cell division now provides the opportunity to elucidate how bacteria 'measure' their energy production to control their proliferation. This proj ....The role of central carbon metabolism in cell cycle control in bacteria. Bacteria are simple organisms, yet we still do not understand how they coordinate their growth with their reproduction so faithfully, generation after generation, to produce viable newborn cells. The new discovery of a link between the food bacteria eat and the first stage of their cell division now provides the opportunity to elucidate how bacteria 'measure' their energy production to control their proliferation. This project combines the latest technology with complementary expertise in bacterial cell division and metabolism. This should identify the mechanism that integrates these fundamental pathways in bacteria, crucial to both their survival and ability to cause infection.Read moreRead less