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biological sciences HONOURs 2014 - The University of Sydney

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MOLECULAR GENETICS<br />

21<br />

Research Interests<br />

Multiresistant strains <strong>of</strong> the bacterial pathogen Staphylococcus<br />

aureus (Golden Staph) are a frequent cause <strong>of</strong> hospitalacquired<br />

infections worldwide, and are an increasing cause <strong>of</strong><br />

serious infections in the wider community. One reason for the<br />

success <strong>of</strong> S. aureus as a hospital pathogen is the resistance<br />

<strong>of</strong> some strains to up to twenty different antimicrobial<br />

compounds, e.g., antibiotics, antiseptics and disinfectants.<br />

In my lab we use genetical, molecular biology, biochemical,<br />

biophysical, cell biology, genomics, functional genomics<br />

and bioinformatic methods to gain an understanding <strong>of</strong> the<br />

genetic basis, mechanisms, and evolution <strong>of</strong> resistance in<br />

staphylococci.<br />

Honours project<br />

1. Functional Analysis <strong>of</strong> Fst-like toxin-antitoxin systems<br />

from S. aureus. We recently identified numerous toxin-antitoxin<br />

(TA) systems on plasmids and chromosomes <strong>of</strong> staphylococci.<br />

Usually these TA systems encode a small protein toxin and<br />

an antisense RNA molecule that serves as an antitoxin by<br />

preventing translation <strong>of</strong> the toxin protein. <strong>The</strong> TA systems<br />

are likely to promote the inheritance <strong>of</strong> resistance plasmids,<br />

even in the absence <strong>of</strong> selection by antibiotics. However, the<br />

Associate Pr<strong>of</strong>essor<br />

Neville Firth<br />

Room 215, Macleay<br />

Building A12<br />

T: (02) 9351 3369<br />

E: neville.firth@sydney.<br />

edu.au<br />

role <strong>of</strong> chromosomally-encoded TA systems is more mysterious. <strong>The</strong> aim <strong>of</strong> this project is to<br />

demonstrate the functionality <strong>of</strong> specific staphylococcal TA systems and to use mutagenesis to<br />

begin to elucidate their mechanism <strong>of</strong> action at the molecular level.

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