https://nova.newcastle.edu.au/vital/access/ /manager/Index en-au 5 PTGS2 (Prostaglandin Endoperoxide Synthase-2) expression in term human amnion in vivo involves rapid mRNA turnover, polymerase-II 5'-pausing, and glucocorticoid transrepression https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:15716 Wed 11 Apr 2018 17:09:52 AEST ]]> Prevalence and Associations of General Practice Registrars' Management of Impetigo: A Cross-Sectional Analysis From the Registrar Clinical Encounters in Training (ReCEnT) Study https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:41967 Tue 16 Aug 2022 14:45:31 AEST ]]> The membrane composition defines the spatial organization and function of a major acinetobacter baumannii drug efflux system https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:43839 Tue 04 Oct 2022 11:46:39 AEDT ]]> An in vitro study on bacterial growth interactions and intestinal epithelial cell adhesion characteristics of probiotic combinations https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:9634 Sat 24 Mar 2018 08:35:23 AEDT ]]> The role of the CopA copper efflux system in acinetobacter baumannii virulence https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:34759 Acinetobacter baumannii has emerged as one of the leading causative agents of nosocomial infections. Due to its high level of intrinsic and adapted antibiotic resistance, treatment failure rates are high, which allows this opportunistic pathogen to thrive during infection in immune-compromised patients. A. baumannii can cause infections within a broad range of host niches, with pneumonia and bacteraemia being associated with the greatest levels of morbidity and mortality. Although its resistance to antibiotics is widely studied, our understanding of the mechanisms required for dealing with environmental stresses related to virulence and hospital persistence, such as copper toxicity, is limited. Here, we performed an in silico analysis of the A. baumannii copper resistome, examining its regulation under copper stress. Using comparative analyses of bacterial P-type ATPases, we propose that A. baumannii encodes a member of a novel subgroup of P1B-1 ATPases. Analyses of three putative inner membrane copper efflux systems identified the P1B-1 ATPase CopA as the primary mediator of cytoplasmic copper resistance in A. baumannii. Using a murine model of A. baumannii pneumonia, we reveal that CopA contributes to the virulence of A. baumannii. Collectively, this study advances our understanding of how A. baumannii deals with environmental copper toxicity, and it provides novel insights into how A. baumannii combats adversities encountered as part of the host immune defence.]]> Fri 01 Apr 2022 09:29:40 AEDT ]]>