Role of Glutathione in Buffering Excess Intracellular Copper in Streptococcus pyogenes

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Abstract
The control of intracellular metal availability is fundamental to bacterial physiology. In the case of copper (Cu), it has been established that rising intracellular Cu levels eventually fill the metal-sensing site of the endogenous Cu-sensing transcriptional regulator, which in turn induces transcription of a copper export pump. This response caps intracellular Cu availability below a well-defined threshold and prevents Cu toxicity. Glutathione, abundant in many bacteria, is known to bind Cu and has long been assumed to contribute to bacterial Cu handling. However, there is some ambiguity since neither its biosynthesis nor uptake is Cu-regulated. Furthermore, there is little experimental support for this physiological role of glutathione beyond measuring growth of glutathione-deficient mutants in the presence of Cu. Our work with group A Streptococcus provides new evidence that glutathione increases the threshold of intracellular Cu availability that can be tolerated by bacteria and thus advances fundamental understanding of bacterial Cu handling.
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Funding Information
  • Royal Society (Research Grant RSG\R1\180044)
  • Garnett Passe and Rodney Williams Memorial Foundation (Research Fellowship)
  • UKRI | Biotechnology and Biological Sciences Research Council (BB/S006818/1)
  • Department of Health, Australian Government | National Health and Medical Research Council
  • Wellcome (Seed Award 214930/Z/18/Z)

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