Affiliation:
1. State Key Laboratory of Plant Diversity and Specialty Crops, Institute of Botany, Chinese Academy of Sciences , Beijing, China
2. China National Botanical Garden , Beijing, China
3. University of Chinese Academy of Sciences , Beijing, China
Abstract
ABSTRACT
Penicillium expansum
is the causal agent of post-harvest blue mold in various fruits and serves as a model for understanding fungal pathogenicity and mycotoxin production. The relevance of oxidative stress response in the growth and virulence of
P. expansum
has been largely unexplored. Here, we identify the transcriptional factor PeAP1 as a regulator of oxidative stress response in
P. expansum
. Gene expression and protein abundance of PeAP1, as well as its nuclear localization, are specifically induced by H
2
O
2
. Deletion of
PeAP1
results in increased sensitivity to H
2
O
2
, and
PeAP1
mutants exhibit a variety of defects in hyphal growth and virulence. PeAP1 prevents the accumulation of both intracellular H
2
O
2
during vegetative growth and host-derived H
2
O
2
during biotrophic growth. Application of an antioxidant glutathione and a NADPH oxidase inhibitor, diphenylene iodonium, to the
PeAP1
mutant partially restored fungal growth and virulence. RNA sequencing analysis revealed 144 H
2
O
2
-induced PeAP1 target genes, including four antioxidant-related genes,
PeGST1
,
PePrx1
,
PePrx2
, and
PeTRX2
, that were also demonstrated to be involved in oxidative stress response and/or virulence. Collectively, our results demonstrate the global regulatory role of PeAP1 in response to oxidative stress and provide insights into the critical role of the PeAP1-mediated oxidative stress response to regulate growth and virulence of
P. expansum
.
IMPORTANCE
Reactive oxygen species are the core of host plant defense and also play a vital role in the successful invasion of host plants by pathogenic fungi. Despite its importance, the relevance of oxidative stress response in fungal growth and virulence is poorly understood in
P. expansum
. In this study, we reveal that the transcription factor PeAP1 acts as a central regulator of oxidative stress response in
P. expansum
and that there is a major link between PeAP1-mediated oxidative stress response and fungal growth and virulence. To explore the underlying mechanisms, we performed comparative transcriptomic studies and identified a number of H
2
O
2
-induced PeAP1 target genes, including four novel ones,
PePrx1
,
PePrx2
,
PeGST1
, and
PeTRX2
, whose functions were linked to PeAP1 and pathogenicity. These findings provide novel insights into the regulation mechanism of PeAP1 on growth and virulence, which might offer promising targets for control of blue mold and patulin contamination.
Funder
MOST | National Natural Science Foundation of China
MOST | National Key Research and Development Program of China
Natural Science Foundation of Beijing Municipality
Science and Technology Commission of Beijing Municipality | Beijing Science and Technology Planning Project
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Cell Biology,Microbiology (medical),Genetics,General Immunology and Microbiology,Ecology,Physiology
Cited by
1 articles.
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