Aug 2026· Frontiers in Plant Science· Vol 17· 0 citations· 36 references
Medicine
TL;DR
Findings underscore a significant role for VdOMO in siderophore-associated iron acquisition, fungal development, stress adaptation, and the early stages of host colonization in V. dahliae.
Abstract
Verticillium dahliae is a soilborne fungal pathogen that causes Verticillium wilt in cotton and many other crops. While siderophore-associated iron acquisition is recognized as crucial, its precise connections to fungal development, stress adaptation, and host colonization remain incompletely elucidated. This study identifies the VdOMO protein as a putative SidA-family L-ornithine N5-monooxygenase through phylogenetic and pairwise sequence analyses. Analyses of independent deletion mutants and a complemented strain showed that VdOMO contributes to conidial morphology and production, microsclerotium formation, and melanization, growth on selected carbon sources, cell wall integrity, and adaptation to alkaline, salt, and oxidative stresses. Although final visible disease symptoms were comparable among inoculated groups, ΔVdOMO mutants exhibited reduced vascular browning, diminished fungal biomass accumulation at early infection stages, and impaired cellophane penetration. A representative ΔVdOMO mutant also displayed decreased biomass-normalized extracellular chrome azurol S (CAS)-reactive iron-chelating activity and intracellular iron accumulation, both of which were restored to wild-type levels upon complementation. Furthermore, VdOMO deletion was linked to iron-condition-dependent alterations in the expression of genes involved in iron regulation, siderophore biosynthesis, and siderophore transport. Collectively, these findings underscore a significant role for VdOMO in siderophore-associated iron acquisition, fungal development, stress adaptation, and the early stages of host colonization in V. dahliae.
Results indicate that VdRgt1 is an important regulator in V. dahliae, coordinating hyphal development, the timing of microsclerotia development and melanin accumulation, carbon and energy metabolism, stress adaptation, and virulence.
It is demonstrated that AaAtg4 is important for spore germination, siderophore biosynthesis, iron acquisition, oxidative stress resistance, and toxin production, thereby establishing its critical role in A. alternata virulence.
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It is demonstrated that VdPRMT1 is required for normal fungal development and full virulence in V. dahliae, and suggested that arginine methylation may contribute to pathogenicity through regulation of RNA processing-related pathways.
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