Isolation and genomic analysis of otomycosis pathogens, and genomics-informed antimicrobial peptide design with

Wenguang Shi1, Jiahao Hu1, Qingru Jiang2

  • 1Shenzhen Key Laboratory of Systems Medicine for Inflammatory Diseases, Zhongshan School of Medicine, Shenzhen Campus of Sun Yat-Sen University, Shenzhen, PR China.

BMC Microbiology
|July 12, 2026
PubMed
Abstract

Insights

This study integrates genomic analysis of Aspergillus terreus causing otomycosis with the development of novel phenylalanine-based peptides. The research identifies antifungal peptide candidates with improved safety and efficacy for treating fungal infections.

Area of Science:

  • Medical Mycology
  • Antimicrobial Drug Discovery
  • Genomics

Background:

  • Superficial fungal infections like otomycosis pose public health challenges due to frequent treatment failures.
  • Inadequate genomic characterization of otomycosis isolates hinders effective treatment strategies.
  • Development of novel antifungal peptides requires integrated assessment of efficacy, safety, and mechanism.

Purpose of the Study:

  • To establish an integrated workflow for characterizing otomycosis-associated Aspergillus terreus isolates using whole genome sequencing.
  • To rationally design and evaluate phenylalanine-based short peptides as potential antifungal agents against A. terreus.
  • To assess the biosafety and membrane permeabilization effects of the designed peptides.

Main Methods:

  • Combined clinical otoscopy, cerumen culture, and whole genome sequencing of an A. terreus AT-1 isolate.
  • Analyzed fungal genome for P450 families, secondary metabolite clusters, pathogenicity factors, and resistance genes.
  • Designed and tested five phenylalanine-based peptides for antifungal activity and membrane permeabilization, including hemolysis assays.

Main Results:

  • Confirmed otomycosis diagnosis and identified A. terreus AT-1 from clinical samples.
  • Genome annotation revealed diverse functional genes related to metabolism, pathogenicity, and resistance.
  • Peptides demonstrated antifungal activity; peptide C3 notably increased A. terreus conidial membrane permeability.

Conclusions:

  • Developed a reproducible workflow linking clinical fungal isolate characterization with genomic data.
  • Successfully identified phenylalanine-based peptides with antifungal potential and distinct safety profiles.
  • This integrated approach supports mechanism-informed development of novel antifungal peptide therapeutics.

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