Related Experiment Video
Updated: Sep 14, 2025

Sexual Crosses with the Mucoromycete Phycomyces blakesleeanus
Published on: June 6, 2025
Proteomic Comparison between Hyphae and Spores Reveals Pathogenicity of Mucor Irregularis
Meijie Zhang1,2, Xiaowei Zhou2,3,4, Yuhan Zhang2,3,4
1Department of Dermatology, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China.
Abstract:
Mucor irregularis, an emerging causative agent of disfiguring mucormycosis, demonstrates distinct clinical manifestations between hyphae and spore forms, though the pathogenic determinants between these two forms remain elusive. Utilizing TMT (tandem mass tag)-based quantitative proteomics (ProteomeXchange: PXD055430), we conducted a comparative analysis of these morphotypes, followed by Gene Ontology (GO)/Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment and protein-protein interaction network construction. Critically, we identified the following: (i) tRNA sulfur modification (NCS6) in spore dormancy maintenance; (ii) adenylate kinase (adenylate kinase 1)-mediated energy metabolism during germination; and (iii) COQ3-dependent mitochondrial function in spore germination. This first proteomic profiling of M. irregularis morphotypes delineates distinct phase-specific adaptations. Notably, the ribosomal and dormancy-associated machinery as NCS6 in spores contrasts sharply with the metabolic activation and upregulated virulence determinants as PAC1 in hyphae. Findings highlight NAT10 critical for spore readiness and RhoGEF GTPases central to hyphal invasion as particularly promising candidate therapeutic targets. Building upon this foundation, future investigations must now delineate the immunomodulatory roles of these effector proteins during host invasion to advance mucormycosis management strategies.
Insights
Mucor irregularis spores and hyphae have distinct adaptations. Researchers identified key proteins like NCS6 and NAT10 involved in spore dormancy and hyphal invasion, offering potential therapeutic targets for mucormycosis.
Area of Science:
- Mycology
- Proteomics
- Infectious Diseases
Background:
- Mucormycosis is a serious fungal infection caused by Mucorales.
- Mucor irregularis presents distinct hyphal and spore forms with unknown pathogenic differences.
- Understanding morphotype-specific adaptations is crucial for managing mucormycosis.
Purpose of the Study:
- To conduct the first proteomic analysis comparing hyphal and spore morphotypes of Mucor irregularis.
- To identify proteins and pathways responsible for phase-specific adaptations.
- To uncover potential therapeutic targets for Mucor irregularis infections.
Main Methods:
- Tandem mass tag (TMT)-based quantitative proteomics was employed for comparative analysis.
- ProteomeXchange accession number PXD055430 was used for data deposition.
- Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses were performed.
- Protein-protein interaction networks were constructed.
Main Results:
- Identified tRNA sulfur modification (NCS6) crucial for spore dormancy.
- Discovered adenylate kinase 1 involvement in energy metabolism during spore germination.
- Found COQ3-dependent mitochondrial function essential for spore germination.
- Highlighted NAT10 in spores and RhoGEF GTPases in hyphae as key players.
Conclusions:
- This study provides the first proteomic insights into Mucor irregularis morphotype differentiation.
- Distinct molecular machinery underlies spore dormancy (e.g., NCS6) and hyphal invasion (e.g., RhoGEF GTPases).
- NAT10 and RhoGEF GTPases represent promising therapeutic targets for mucormycosis treatment.
Related Concept Videos
Fungal Group Zygomycota
Fungal Phylum Microsporidia
Fungal Phylum Basidiomycota
Fungal Phylum Ascomycota
Overview of Fungi

