Potent Antimicrobial Activity of Aspergillus oryzae Fermentate Against Toxigenic Strains of Clostridioides difficile

Ahmad Alshannaq1, Morgan Henning1,2, Jonah Dixon1,2

  • 1School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI 53706, USA.

PubMed

Insights

A novel fungal extract from Aspergillus oryzae shows potent bactericidal activity against Clostridioides difficile, offering a promising new avenue for treating C. difficile infections.

Area of Science:

  • Microbiology
  • Mycology
  • Infectious Diseases

Background:

  • Clostridioides difficile infection (CDI) presents a significant public health concern in the US.
  • Limited effective treatment options are currently available for CDI.
  • Novel antimicrobial strategies are urgently needed.

Purpose of the Study:

  • To evaluate the antimicrobial efficacy of a fungal fermentate from Aspergillus oryzae against toxigenic C. difficile strains.
  • To compare the activity of the fungal extract with vancomycin.
  • To elucidate the mechanism of action of the fungal extract against C. difficile.

Main Methods:

  • Ethyl acetate extract of A. oryzae fermentate was prepared.
  • Antimicrobial activity was assessed using zone of inhibition assays and time-kill kinetics.
  • Mechanism of action was investigated using scanning electron microscopy and flow cytometry.

Main Results:

  • The fungal extract demonstrated potent bactericidal activity against all tested C. difficile strains, including Ribotype 027.
  • The extract showed greater efficacy than vancomycin against 80% of the tested strains.
  • Microscopic and flow cytometry analyses revealed membrane disruption, intracellular leakage, and cell lysis.
  • Complete C. difficile eradication was achieved within six hours in time-kill assays.

Conclusions:

  • The fungal extract of A. oryzae possesses significant antimicrobial activity against C. difficile.
  • The extract acts by disrupting the bacterial cell membrane, leading to lysis.
  • Further research is warranted to identify active compounds and assess in vivo efficacy for potential clinical application in CDI management.

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