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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.
Background:
Fungal infections are increasingly recognized as a major public health challenge, and superficial diseases such as otomycosis remain clinically consequential because persistence, recurrence, and treatment failure are common when the causative species and susceptibility profile are not clearly defined. However, otomycosis associated isolates are often insufficiently characterized at the genomic level. Furthermore, the development of antifungal candidates, particularly for short antimicrobial peptides, remains heterogeneous in terms of the integration of efficacy, biosafety, and mechanistic endpoints.
Methods:
Here, we combined clinical otoscopy and cerumen culture with whole genome sequencing and multi-database annotation of an otomycosis derived Aspergillus terreus AT-1 isolate, including targeted analyses of cytochrome P450 families, secondary metabolite biosynthetic gene clusters, curated pathogenicity resources, and antimicrobial/antibiotic resistance signatures. Then, we rationally designed five C-terminally amidated, phenylalanine based short peptides with controlled physicochemical parameters and assessed antifungal activity by broth microdilution MIC assays against A. terreus AT-1 and yeast pathogens, complemented by hemolysis testing and propidium iodide based flow cytometry and microscopy to evaluate membrane permeabilization.
Results:
Otoscopy was consistent with otomycosis, and culture yielded colonies identified as A. terreus AT-1 from the affected ear but not from recovered controls. Genome annotation defined a functionally diverse repertoire spanning metabolism, transport, secondary metabolism, pathogenicity linked features, and a structured resistance gene landscape. The peptide panel showed measurable antifungal activity with distinct hemolysis profiles, and peptide C3 increased A. terreus AT-1 conidial membrane permeability.
Conclusions:
Overall, this study establishes an integrated and reproducible workflow that couples clinical isolation and genome resolved characterization of an otomycosis associated A. terreus AT-1 isolate with biosafety aware, mechanism informed triage of phenylalanine based short peptides.
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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