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Toxins 2016, 8(5), 140;

Toxin-Antitoxin Systems of Staphylococcus aureus

Section of Microbiology & MRC Centre for Molecular Bacteriology and Infection, Imperial College London, London SW7 2AZ, UK
Interfakultäres Institut für Mikrobiologie und Infektionsmedizin, Lehrbereich Mikrobielle Genetik, University of Tübingen, 72076 Tübingen, Germany
Klinikum Nürnberg Medical School GmbH, Research Department, Paracelsus Medical University, 90419 Nuremberg, Germany
These authors contributed equally to this work.
Author to whom correspondence should be addressed.
Academic Editor: Yinduo Ji
Received: 28 February 2016 / Revised: 21 April 2016 / Accepted: 25 April 2016 / Published: 5 May 2016
(This article belongs to the Collection Staphylococcus aureus Toxins)
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Toxin-antitoxin (TA) systems are small genetic elements found in the majority of prokaryotes. They encode toxin proteins that interfere with vital cellular functions and are counteracted by antitoxins. Dependent on the chemical nature of the antitoxins (protein or RNA) and how they control the activity of the toxin, TA systems are currently divided into six different types. Genes comprising the TA types I, II and III have been identified in Staphylococcus aureus. MazF, the toxin of the mazEF locus is a sequence-specific RNase that cleaves a number of transcripts, including those encoding pathogenicity factors. Two yefM-yoeB paralogs represent two independent, but auto-regulated TA systems that give rise to ribosome-dependent RNases. In addition, omega/epsilon/zeta constitutes a tripartite TA system that supposedly plays a role in the stabilization of resistance factors. The SprA1/SprA1AS and SprF1/SprG1 systems are post-transcriptionally regulated by RNA antitoxins and encode small membrane damaging proteins. TA systems controlled by interaction between toxin protein and antitoxin RNA have been identified in S. aureus in silico, but not yet experimentally proven. A closer inspection of possible links between TA systems and S. aureus pathophysiology will reveal, if these genetic loci may represent druggable targets. The modification of a staphylococcal TA toxin to a cyclopeptide antibiotic highlights the potential of TA systems as rather untapped sources of drug discovery. View Full-Text
Keywords: Staphylococcus aureus; toxin-antitoxin system; plasmid addiction; MazEF; YefM-YoeB; RNase; SprA1-SprA1AS; SprFG; TenpIN; Omega-Epsilon-Zeta Staphylococcus aureus; toxin-antitoxin system; plasmid addiction; MazEF; YefM-YoeB; RNase; SprA1-SprA1AS; SprFG; TenpIN; Omega-Epsilon-Zeta

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Schuster, C.F.; Bertram, R. Toxin-Antitoxin Systems of Staphylococcus aureus. Toxins 2016, 8, 140.

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