Melissa Brown

Professor
Biological Sciences
Flinders University
Australia

Professor Microbiology
Biography

Prof Brown completed her B.Sc. (Hons.) and her PhD. in the Department of Microbiology and Immunology at Adelaide University under the guidance of Prof Paul Manning and A/Prof Renato Morona. She undertook postdoctoral training with Prof Robert Hancock at the University of British Columbia in Canada for which she was awarded a Canadian Cystic Fibrosis Foundation Postdoctoral Fellowship. Prof Brown returned to Australia in 1993 to work with Prof Ronald Skurray at the University of Sydney. In 2007 she relocated her laboratory to Flinders University where she is currently Professor in Microbiology.

Research Intrest

The overall scientific goal of the research undertaken in Prof Brown's laboratory is to determine the complex mechanisms used by bacteria to evade strategies employed by the host for their elimination, including the use of antimicrobial agents. Drug-resistant microorganisms are a major worldwide health issue as a number of important human pathogens have now acquired mechanisms that make them largely resistant to all currently available treatment regimes. One of the most significant resistance mechanisms involves membrane-bound efflux pumps that actively transport toxic antimicrobial compounds from the bacterial cell before they reach their intracellular target. Although many export systems transport a single substrate, or a small group of structurally-related substrates, a number of multidrug resistance (MDR) export systems are involved in the efflux of a wide range of structurally-dissimilar antimicrobial compounds. These MDR pumps are widespread amongst pathogenic bacteria and fungi, parasitic protozoa, and human tumour cells. With her team she is investigating the molecular structures, mechanistic processes and molecular evolution of these efflux pumps. Together with international collaborators, they have provided insights into the controversy of how proteins bind multiple ligands.

List of Publications
Ni, L., Jensen, S., Tonthat, N.K., Berg, T., Kwong, S., Guan, F.H.X., et al. (2009). The Staphylococcus aureus pSK41 plasmid-encoded ArtA protein is a master regulator of plasmid transmission genes and contains a RHH motif used in alternate DNA-binding modes. Nucleic Acids Research, 37(20) pp. 6970-6983.
Peters, K., Brooks, B., Schumacher, M., Skurray, R., Brennan, R. and Brown, M.H. (2011). A single acidic residue can guide binding site selection but does not govern QacR cationic-drug affinity. PLoS One, 6(1) pp. e15974.
Eijkelkamp, B.A., Hassan, K., Paulsen, I. and Brown, M.H. (2011). Development of a high-throughput cloning strategy for characterization of Acinetobacter baumannii drug transporter proteins. Journal of Molecular Microbiology and Biotechnology, 20(4) pp. 211-219.
Farrugia, D., Elbourne, L., Hassan, K., Eijkelkamp, B., Tetu, S., Brown, M.H., et al. (2013). The complete genome and phenome of a community-acquired Acinetobacter baumannii. PLoS One, 8(3) pp. e58628
Eijkelkamp, B., Stroeher, U., Hassan, K., Elbourne, L., Paulsen, I. and Brown, M.H. (2013). H-NS plays a role in expression of the Acinetobacter baumannii persistence and virulence features. Infection and Immunity, 81(7) pp. 2574-2583.