Staphylococcus aureus Preferentially Liberates Inorganic Phosphate from Organophosphates in Environments where This

Jessica L Kelliher1, Aleeza J Leder Macek1, Kevin M Grudzinski1

  • 1Department of Microbiology, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.

Journal of Bacteriology
|September 2, 2020
PubMed

Insights

Staphylococcus aureus utilizes various organic phosphate compounds as essential nutrient sources during infection. The bacteria primarily release inorganic phosphate (Pi) extracellularly using the phosphatase PhoB before importing it via Pi transporters.

Area of Science:

  • Microbiology
  • Nutrient Acquisition
  • Pathogenesis

Background:

  • Phosphate is crucial for bacterial survival and virulence.
  • Staphylococcus aureus requires phosphate acquisition from the host during infection.
  • Phosphate-limiting conditions during infection necessitate alternative phosphate sources.

Purpose of the Study:

  • To identify organophosphate compounds that support Staphylococcus aureus growth.
  • To elucidate the mechanisms by which S. aureus utilizes organophosphates for phosphate acquisition.
  • To investigate the role of the phosphatase PhoB and Pi transporters in utilizing alternative phosphate sources.

Main Methods:

  • Screening of 58 phosphorus-containing molecules for their ability to support S. aureus growth.
  • Genetic analysis of PhoB- and Pi transporter-deficient S. aureus strains.
  • Assessing bacterial growth on various organophosphate substrates.

Main Results:

  • 46 out of 58 tested compounds supported S. aureus growth.
  • Glycerol-3-phosphate (G3P) is a significant organophosphate source.
  • A majority of organophosphate utilization relies on extracellular processing by PhoB and subsequent import via Pi transporters.

Conclusions:

  • Staphylococcus aureus can utilize a wide array of organophosphates as phosphate sources.
  • The PhoB phosphatase and Pi transporters are critical for efficient phosphate acquisition from diverse organic sources.
  • Understanding these mechanisms is vital for targeting S. aureus infections in phosphate-limited host environments.

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