Botrytis cinerea
is a typical necrotrophic plant pathogenic fungus which can deliberately acidify host tissues and trigger oxidative bursts therein to facilitate its virulence. The white collar complex (WCC), consisting of BcWCL1 and BcWCL2, is recognized as the primary light receptor in
B. cinerea
. Nevertheless, the specific mechanisms through which the WCC components, particularly BcWCL2 as a GATA transcription factor, control virulence are not yet fully understood. This study demonstrates that deletion of BcWCL2 results in the loss of light-sensitive phenotypic characteristics. Additionally, the Δ
bcwcl2
strain exhibits reduced secretion of citrate, delayed infection cushion development, weaker hyphal penetration, and decreased virulence. The application of exogenous citric acid was found to restore infection cushion formation, hyphal penetration, and virulence of the Δ
bcwcl2
strain. Transcriptome analysis at 48 h post-inoculation revealed that two citrate synthases, putative citrate transporters, hydrolytic enzymes, and reactive oxygen species scavenging-related genes were down-regulated in Δ
bcwcl2
, whereas exogenous citric acid application restored the expression of the above genes involved in the early infection process of Δ
bcwcl2
. Moreover, the expression of
Bcvel1
, a known regulator of citrate secretion, tissue acidification, and secondary metabolism, was down-regulated in Δ
bcwcl2
but not in Δ
bcwcl1
. ChIP-qPCR and electrophoretic mobility shift assays revealed that BcWCL2 can bind to the promoter sequences of
Bcvel1
. Overexpressing
Bcvel1
in Δ
bcwcl2
was found to rescue the mutant defects. Collectively, our findings indicate that BcWCL2 regulates the expression of the global regulator
Bcvel1
to influence citrate secretion, tissue acidification, redox homeostasis, and virulence of
B. cinerea
.
IMPORTANCE
This study illustrated the significance of the fungal blue light receptor component BcWCL2 protein in regulating citrate secretion in
Botrytis cinerea
. Unlike BcWCL1, BcWCL2 may contribute to redox homeostasis maintenance during infection cushion formation, ultimately proving to be essential for full virulence. It is also demonstrated that BcWCL2 can regulate the expression of
Bcvel1
to influence host tissue acidification, citrate secretion, infection cushion development, and virulence. While the role of organic acids secreted by plant pathogenic fungi in fungus-host interactions has been recognized, this paper revealed the importance, regulatory mechanisms, and key transcription factors that control organic acid secretion. These understanding of the pathogenetic mechanism of plant pathogens can provide valuable insights for developing effective prevention and treatment strategies against fungal diseases.