Augmentation of microsporidia adherence and host cell infection by divalent cations

Timothy R Southern1, Carrie E Jolly, J Russell Hayman

  • 1Department of Microbiology, James H. Quillen College of Medicine, East Tennessee State University, Johnson City, TN 37614, USA.

Insights

Divalent cations like manganese and magnesium enhance microsporidia spore adherence and infection of host cells. This suggests these cations play a key role in the microsporidia infection process.

Area of Science:

  • Microbiology
  • Cell Biology
  • Infectious Diseases

Background:

  • Microsporidia are opportunistic intracellular pathogens.
  • Spore adherence to host cells, mediated by sulfated glycosaminoglycans, is crucial for infection.
  • The precise mechanism of spore activation and polar filament discharge remains unclear.

Purpose of the Study:

  • To investigate the impact of exogenous divalent cations on microsporidia spore adherence.
  • To determine the effect of divalent cations on host cell infection rates.
  • To elucidate the role of divalent cations in the microsporidia infection pathway.

Main Methods:

  • In vitro spore adherence assay.
  • Evaluation of spore adherence in the presence of manganese (Mn2+), magnesium (Mg2+), and calcium (Ca2+).
  • Assessment of host cell infection efficiency with and without divalent cations.

Main Results:

  • Spore adherence was significantly increased by Mn2+ and Mg2+, but not by Ca2+.
  • All tested divalent cations (Mn2+, Mg2+, Ca2+) enhanced host cell infection.
  • Mn2+ and Mg2+ appear to activate a component on the microsporidia spore itself, not the host cell.

Conclusions:

  • Divalent cations, particularly Mn2+ and Mg2+, are critical for augmenting microsporidia spore adherence and subsequent host cell infection.
  • Spore adherence is a vital step in the microsporidia infection process, influenced by specific cation interactions.
  • The findings provide insights into the molecular mechanisms underlying microsporidia pathogenesis and potential therapeutic targets.

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