Novel Antiamoebic Tyrocidine-Derived Peptide against Brain-Eating Amoebae

Noor Akbar1, Wendy E Kaman2, Maarten Sarink3

  • 1College of Arts and Sciences, American University of Sharjah, University City, Sharjah 26666, United Arab Emirates.

ACS Omega
|August 29, 2022
PubMed

Insights

A novel tyrocidine-derived peptide shows potent activity against Acanthamoeba castellanii and Naegleria fowleri, two dangerous amoebae. This peptide effectively reduces amoebae viability and inhibits their ability to infect human cells, offering a promising new therapeutic avenue.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Drug Discovery

Background:

  • Acanthamoeba castellanii (A. castellanii) causes sight-threatening Acanthamoeba keratitis and fatal granulomatous amoebic encephalitis.
  • Naegleria fowleri (N. fowleri) causes deadly primary amoebic encephalitis, primarily through waterborne exposure.
  • Both infections have mortality rates exceeding 90%, highlighting an urgent need for alternative treatments.

Purpose of the Study:

  • To evaluate the antiamoebic activity of a tyrocidine-derived peptide against A. castellanii and N. fowleri.
  • To assess the peptide's efficacy in reducing amoebic viability, adhesion, and cytopathogenicity.
  • To investigate the peptide's effect on amoebic encystation and its cytotoxicity to human cells.

Main Methods:

  • Testing the antiamoebic activity of a tyrocidine-derived peptide against A. castellanii and N. fowleri in vitro.
  • Assessing amoebic viability, adherence to human cells, and cytopathogenicity following peptide treatment.
  • Evaluating the peptide's impact on amoebic encystation and its cytotoxicity to human cells.

Main Results:

  • The tyrocidine-derived peptide demonstrated significant amoebicidal efficacy, drastically reducing amoebae viability within 2-24 hours.
  • The peptide inhibited amoebic adherence to human cells and reduced amoeba-mediated cell damage.
  • Significant inhibition of encystation was observed for both A. castellanii and N. fowleri, with minimal cytotoxicity to human cells.

Conclusions:

  • The tyrocidine-derived peptide exhibits potent antiamoebic activity against A. castellanii and N. fowleri.
  • The peptide effectively inhibits key pathogenic mechanisms, including viability, adhesion, and encystation.
  • This peptide represents a promising candidate for developing novel treatments against severe free-living amoebae infections.

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