The Verticillium dahliae Small Cysteine-Rich Protein VdSCP23 Manipulates Host Immunity

Verticillium wilt caused by Verticillium dahliae is a notorious soil-borne fungal disease and seriously threatens the yield of economic crops worldwide. During host infection, V. dahliae secretes many effectors that manipulate host immunity, among which small cysteine-rich proteins (SCPs) play an important role. However, the exact roles of many SCPs from V. dahliae are unknown and varied. In this study, we show that the small cysteine-rich protein VdSCP23 inhibits cell necrosis in Nicotiana benthamiana leaves, as well as the reactive oxygen species (ROS) burst, electrolyte leakage and the expression of defense-related genes. VdSCP23 is mainly localized in the plant cell plasma membrane and nucleus, but its inhibition of immune responses was independent of its nuclear localization. Site-directed mutagenesis and peptide truncation showed that the inhibition function of VdSCP23 was independent of cysteine residues but was dependent on the N-glycosylation sites and the integrity of VdSCP23 protein structure. Deletion of VdSCP23 did not affect the growth and development of mycelia or conidial production in V. dahliae. Unexpectedly, VdSCP23 deletion strains still maintained their virulence for N. benthamiana, Gossypium hirsutum and Arabidopsis thaliana seedlings. This study demonstrates an important role for VdSCP23 in the inhibition of plant immune responses; however, it is not required for normal growth or virulence in V. dahliae.

Automated summary

This study shows that the small cysteine-rich protein VdSCP23 from Verticillium dahliae can inhibit cell necrosis, reactive oxygen species burst, electrolyte leakage, and the expression of defense-related genes in Nicotiana benthamiana. Localization analysis reveals that VdSCP23 is mainly located in the plasma membrane and nucleus of plant cells. The inhibition of immune responses by VdSCP23 is not dependent on its nuclear localization or cysteine residues, but on N-glycosylation sites and the integrity of protein structure.