Genome analysis shows that pcwdes regulate hyphal growth and conidiation in Verticillium dahliae, indicating a critical role in pathogenicity.
Verticillium wilt, a soil-borne fungal disease caused by Verticillium dahliae, is a major threat to agricultural production. The plant cell wall serves as the primary barrier against the invasion of fungal pathogens. To facilitate successful infection, many pathogens encode plant cell wall-degrading enzymes (PCWDEs) to degrade cell wall components. In this study, we conducted a genome-wide analysis of PCWDE gene families in two V.dahliae strains, VdSHZ-4 and VdSHZ-9, with different pathogenicity. VdSHZ-4 and VdSHZ-9 genomes were found to contain 415 and 396 PCWDE genes, respectively. We successfully isolated two key enzymes from V. dahliae: the cutinase VdCut1 and the pectin lyase VdPL16. To investigate the functions of these two genes, we constructed VdCut1 and VdPL16 deletion and complementation mutants and examined their roles in hyphal growth, conidiation, and pathogenicity toward cotton Verticillium wilt. Results showed that deletion of VdCut1 or VdPL16 suppressed colony growth and reduced conidial production, and it also impaired the utilization of sucrose and galactose and markedly increased sensitivity to abiotic stresses such as sodium dodecyl sulfate (SDS) and sorbitol. The VdCut1 deletion mutant completely lost the ability to penetrate cellophane membranes, whereas the VdPL16 deletion mutant exhibited significantly reduced penetration capacity. Both deletions markedly attenuated virulence, with the loss of VdCut1 having the more pronounced effect. In planta colonization assays revealed that the VdCut1 mutant accumulated much less biomass in host tissues than the wild-type strain and the VdPL16 mutant. These findings demonstrate that VdCut1 and VdPL16 play critical roles in V.dahliae pathogenicity by regulating hyphal growth and conidiation. The results deepen our understanding of the molecular mechanisms by which this pathogen degrades plant cell walls and provide a theoretical basis for antifungal strategies that target plant cell wall-degrading enzymes (PCWDEs).
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Asigul Ismayil (2025) studied this question.
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