Infectious Disease

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Infectious Disease Infectious Disease – a 21st Century Challenge The ithree institute based at the University of Technology Sydney (UTS) brings together an Internationally competitive team focused on addressing key challenges in the understanding and control of infectious diseases in humans and animals. The institute’s innovative science uses a systems biology approach to develop a greater insight into basic biology and its application to the diagnosis, treatment and prevention of infectious diseases. Our Research Focus: ‘One Health’ Despite decades of groundbreaking research and the development of new medicines including vaccines and antibiotics, infectious diseases remain an important global animal and human health issue, posing a major problem to the wealth and wellbeing of nations. At the ithree institute, we are at the forefront of understanding the importance of the interplay of pathogens, in both human and animal hosts, and the environment – the so called One Health model. Our inter-disciplinary approach to basic and translational research to understand this ‘infectious ecology’ will underpin the development of new solutions to infectious disease challenges that include: • The changing geographical distribution of diseases due to economic migration, global mobility and the impact of climate change • The emergence of new pathogens • The threat to health from zoonosis • An increasing number of antibiotic and drug resistant pathogens • The potential threat to biosecurity including natural pandemics The ithree institute has active research programs and collaborations in the fields of bacteriology, parasitology and virology. Our Facilities: Systems Biology The ithree institute occupies new state-of-the-art laboratories in central Sydney, including facilities for pathogen culture. The institute has particular expertise in molecular biology, cell biology, genetics, bioinformatics and protein chemistry, and has invested in a world-class Microbial Imaging Facility that provides OMX super resolution imagery and a Microbial Proteomics suite. These facilities are available for both collaborative and contract research. Our Approach: Collaborative Research The core philosophy at the ithree institute is to work in partnership with others to delivery world-class scientific discovery and to drive innovation. We have established relationships with universities, research institutes, medical institutes and industry, both within Australia and Internationally. www.ithree institute.uts.edu.au Our Research Area: Bacteriology The ithree institute is led by Professor Ian Charles, an internationally recognised expert in the field of infectious diseases with a track record of driving innovation both within academia and within industry. It consists of research groups led by globally experienced scientists in the fields of microbial and parasitic infectious diseases, and in the application of their basic research to the treatment and prevention of these diseases. Group Leader Research Focus Prof. Ian Charles • Founding scientist and board level experience in a medical research institute at UCL, London, UK • Co-founder and CSO of a biotech spin-out company, Arrow Therapeutics, UK • Basic and applied research leading to new vaccines and anti-infectives Prof. Harold Stokes • Immediate Past President of the Australian Society for Microbiology • Developed the concept of the ‘integron’ and its role in bacterial adaptation • Expert on integrons, mobile gene cassettes and pathogencity in Vibrio cholerae Associate Prof. Elizabeth Harry • Vice President Scientific Affairs for the Australian Society for Microbiology • International authority on bacterial cell biology • Expert on the understanding of antibiotic action Associate Prof. Cynthia • NHMRC Senior Research Fellow Whitchurch • Founding Director of the Microbial Imaging facility • Basic and applied research in biofilms, bacterial cell biology, host-pathogen interactions, collective behaviours Associate Prof. Steven • International expert in the post-translational modifications to mycoplasmal adhesins using proteomics Djordjevic • Pioneer in the identification of vaccine antigens to control mycoplasmal pathogens • Pioneer in the assessment of non-needle delivery of vaccine antigens that stimulate mucosal immunity Track Record: Our Scientists’ Success Snap-shots New Vaccines Integrons Surface Antigens Biofilms Figure. Structure of P69 Figure. Structure of an integron- Figure. Interaction between M. Figure. Biofilm with DNA Pertactin encoded member of the hyopneumoniae and the Biofilms are multicellular Pertactin is a component of the dechlorinase family surface of a porcine epithelial- communities of bacteria acellular petussis vaccine that is Integrons may help bacteria like cell monolayer embedded in a self-produced used to protect people from become pathogenic and resistant On its cell surface, M. matrix comprised of extracellular whooping cough. to antibiotics. hyopneumoniae displays two polymeric substances (slime) that Ref : P Emsley, IG Charles , NF Ref : Y Boucher, M Labbate, JE adhesin families that are targets includes DNA. Fairweather & NW Isaacs. 1996. Koenig and HW Stokes. 2007. for proteolytic cleavage and other Ref: CB Whitchurch, T Tolker- Nature, 381: 90-92. Trends in Microbiology, 15: 301- posttranslational modification Nielsen, PC Ragas, and JS events that influence their function. 309. Mattick. 2002. Science, 22: 148. Ref: TA Burnett, (10 authors) & SP Djordjevic. (2006) Molecular Microbiology, 60: 669-686. Working in Partnership We welcome the opportunity to explore research collaborations, partnerships, licensing and spin outs to work together to meet the 21st Century challenges in infectious disease. ithree institute, University of Technology, Sydney, P.O.Box 123, Broadway, NSW 2007, Australia UTS CRICOS Provider Code: 00099F t: +61 2 9514 4200 e: [email protected] .
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  • Showcase Page
    SHOWCASE ON RESEARCH EDITORIAL Excellence and Breadth: the Success of Cytoskeleton Research in Australia and New Zealand The Molecular Biology of the Cell textbook used to include value of diverse experimental approaches that each an advisory to students: “The functions of the cytoskeleton provide a unique insight. These include in vitro assays of are difficult to study”. For the cautious, this sounds like sage cytoskeleton assembly/disassembly and cytoskeleton-based advice. When their research encounters the cytoskeleton, they cargo movement, structural biology, microscopic imaging, will search for a detour around this difficult topic. However, study of inherited diseases and genetic studies employing for the adventurous, exploration of the cytoskeleton is the model organisms. More recently, omic approaches have ultimate challenge – a cell biologist’s ascent of Everest. identified novel cytoskeleton genes and proteins, and have The cytoskeleton is central to cell biology. It dictates the demonstrated altered expression of cytoskeleton components shape of each individual cell, as well as the whole multicellular in both inherited and acquired diseases. organism. It is responsible for the polarised distribution of This Showcase aims to provide the broadest possible organelles, proteins and RNA within cells. It is also responsible coverage of cytoskeleton research. Liz Harry and Leigh for the pattern by which cells proliferate to form tissues, the Monahan describe how a prototype cytoskeleton (only adherence of cells to each other and the extracellular matrix, recently recognised in prokaryotes), comprising an actin and and the chemotactic motility and polarised growth of cells. a tubulin homologue, forms intriguing spiral-shape structures Without the cytoskeleton, cells would be an amorphous that help determine where cell division initiates.
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  • Coordination of Chromosome Segregation and Cell Division in Staphylococcus Aureus
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  • Light Microscopy Techniques for Bacterial Cell Biology Petra Anne
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  • The Bacterial Cytoskeleton
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  • Superfast Evolution of Bacterial Resistance to Beta-Lactam Antibiotics
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  • The Bulletin 372
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  • Extracellular Signal Protein Triggering the Proteolytic Activation of a Developmental Transcription Factor in B
    View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector Cell, Vol. 63, 219-226, October 20, 1995, Copyright 0 1995 by Cell Press Extracellular Signal Protein Triggering the Proteolytic Activation of a Developmental Transcription Factor in B. subtilis Antje E. M. Hofmeister, l Arturo Londofio-VaNejo,? has been engulfed by the mother cell, oG and eK become Elizabeth Harry, l Patrick Stragier,t the principal determinants of gene transcription in thefore- and Richard Losick* spore and the mother cell, respectively. Thus, as morpho- *Department of Molecular and Cellular Biology genesis progresses the compartments follow two parallel The Biological Laboratories but dissimilar lines of gene expression, involving the suc- Harvard University cessive action of oF and dG in the forespore and dE and Cambridge, Massachusetts 02138 dK in the mother cell. flnstitut de Biologie Physico-Chimique Although each compartment follows its own program of 13, rue Pierre et Marie Curie cellular differentiation, the forespore and mother cell lines 75005 Paris of gene transcription do not proceed wholly independently France of one another. Rather, gene transcription in the mother cell is tied to events in the forespore by two different signal transduction pathways operating at late (Cutting et al., Summary 1990) and early (Karow et al., 1995; LondoAo-Vallejo and Stragier, 1995; Losick and Stragier, 1992; Margolis et al., We present biochemical evidence for an intercellular 1991) stages of morphogenesis. The late-stage pathway signal transduction pathway in B. subtilis. This path- involves the coupling of the appearance of qK in the mother way governs the conversion of the proprotein pro-8 cell totheactionofoGin theforespore(Cuttingetal., 1990).
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  • Coordinating Bacterial Cell Division with Nutrient Availability: a Role Mbio.Asm.Org for Glycolysis on February 26, 2015 - Published by Leigh G
    Downloaded from RESEARCH ARTICLE Coordinating Bacterial Cell Division with Nutrient Availability: a Role mbio.asm.org for Glycolysis on February 26, 2015 - Published by Leigh G. Monahan,a Isabella V. Hajduk,a Sinead P. Blaber,b Ian G. Charles,a Elizabeth J. Harrya The ithree institute, University of Technology, Sydney, New South Wales, Australiaa; Department of Chemistry and Biomolecular Sciences, Macquarie University, North Ryde, New South Wales, Australiab ABSTRACT Cell division in bacteria is driven by a cytoskeletal ring structure, the Z ring, composed of polymers of the tubulin-like protein FtsZ. Z-ring formation must be tightly regulated to ensure faithful cell division, and several mechanisms that influence the positioning and timing of Z-ring assembly have been described. Another important but as yet poorly understood aspect of cell division regulation is the need to coordinate division with cell growth and nutrient availability. In this study, we demon- strated for the first time that cell division is intimately linked to central carbon metabolism in the model Gram-positive bacte- rium Bacillus subtilis. We showed that a deletion of the gene encoding pyruvate kinase (pyk), which produces pyruvate in the final reaction of glycolysis, rescues the assembly defect of a temperature-sensitive ftsZ mutant and has significant effects on Z-ring formation in wild-type B. subtilis cells. Addition of exogenous pyruvate restores normal division in the absence of the mbio.asm.org pyruvate kinase enzyme, implicating pyruvate as a key metabolite in the coordination of bacterial growth and division. Our re- sults support a model in which pyruvate levels are coupled to Z-ring assembly via an enzyme that actually metabolizes pyruvate, the E1␣ subunit of pyruvate dehydrogenase.
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  • Print Special Issue Flyer
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  • Rapid Antibacterial Activity of Cannabichromenic Acid Against Methicillin-Resistant Staphylococcus Aureus
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  • Urinary Tract Infections: Uncommon Solutions for a Common Problem
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  • A Newly Identified Prophage-Encoded Gene, Ymfm, Causes SOS-Inducible Filamentation
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