Overlapping functionality of the pht proteins in zinc homeostasis of Streptococcus pneumoniae

Charles D. Plumptre, Catherine E. Hughes, Richard M. Harvey, Bart A. Eijkelkamp, Christopher A. McDevitt, James C. Paton

Research output: Contribution to journalArticle

20 Citations (Scopus)

Abstract

Streptococcus pneumoniae is a globally significant pathogen that causes a range of diseases, including pneumonia, sepsis, meningitis, and otitis media. Its ability to cause disease depends upon the acquisition of nutrients from its environment, including transition metal ions such as zinc. The pneumococcus employs a number of surface proteins to achieve this, among which are four highly similar polyhistidine triad (Pht) proteins. It has previously been established that these proteins collectively aid in the delivery of zinc to the ABC transporter substrate-binding protein AdcAII. Here we have investigated the contribution of each individual Pht protein to pneumococcal zinc homeostasis by analyzing mutant strains expressing only one of the four pht genes. Under conditions of low zinc availability, each of these mutants showed superior growth and zinc accumulation profiles relative to a mutant strain lacking all four genes, indicating that any of the four Pht proteins are able to facilitate delivery of zinc to AdcAII. However, optimal growth and zinc accumulation in vitro and pneumococcal survival and proliferation in vivo required production of all four Pht proteins, indicating that, despite their overlapping functionality, the proteins are not dispensable without incurring a fitness cost. We also show that surface-attached forms of the Pht proteins are required for zinc recruitment and that they do not contribute to defense against extracellular zinc stress.

Original languageEnglish
Pages (from-to)4315-4324
Number of pages10
JournalInfection and Immunity
Volume82
Issue number10
DOIs
Publication statusPublished - Oct 2014
Externally publishedYes

Keywords

  • Streptococcus pneumoniae
  • disease
  • surface proteins
  • polyhistidine triad (Pht) proteins

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