Time-Course Transcriptome Profiling Reveals Differential Resistance Responses of Tomato to a Phytotoxic Effector of the Pathogenic Oomycete Phytophthora cactorum

被引:2
|
作者
Zhou, Xue [1 ]
Wen, Ke [1 ]
Huang, Shen-Xin [1 ]
Lu, Yi [1 ]
Liu, Yang [1 ,2 ]
Jin, Jing-Hao [1 ,2 ]
Kale, Shiv D. [3 ]
Chen, Xiao-Ren [1 ,2 ]
机构
[1] Yangzhou Univ, Coll Plant Protect, 48 Eastern Wenhui Rd, Yangzhou 225009, Peoples R China
[2] Yangzhou Univ, Joint Int Res Lab Agr & Agriprod Safety Minist Edu, 48 Eastern Wenhui Rd, Yangzhou 225009, Peoples R China
[3] Virginia Tech, Fralin Life Sci Inst, Blacksburg, VA 24060 USA
来源
PLANTS-BASEL | 2023年 / 12卷 / 04期
基金
中国国家自然科学基金;
关键词
tomato; transcriptome; Phytophthora cactorum; small cysteine-rich protein; phytotoxicity; defense response; PAMP-TRIGGERED IMMUNITY; EXPRESSION ANALYSIS; PROTEIN PCF; FAMILY; INFECTION; DEFENSE; STRESS; GENES;
D O I
10.3390/plants12040883
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Blight caused by Phytophthora pathogens has a devastating impact on crop production. Phytophthora species secrete an array of effectors, such as Phytophthora cactorum-Fragaria (PcF)/small cysteine-rich (SCR) phytotoxic proteins, to facilitate their infections. Understanding host responses to such proteins is essential to developing next-generation crop resistance. Our previous work identified a small, 8.1 kDa protein, SCR96, as an important virulence factor in Phytophthora cactorum. Host responses to SCR96 remain obscure. Here, we analyzed the effect of SCR96 on the resistance of tomato treated with this recombinant protein purified from yeast cells. A temporal transcriptome analysis of tomato leaves infiltrated with 500 nM SCR96 for 0, 3, 6, and 12 h was performed using RNA-Seq. In total, 36,779 genes, including 2704 novel ones, were detected, of which 32,640 (88.7%) were annotated. As a whole, 5929 non-redundant genes were found to be significantly co-upregulated in SCR96-treated leaves (3, 6, 12 h) compared to the control (0 h). The combination of annotation, enrichment, and clustering analyses showed significant changes in expression beginning at 3 h after treatment in genes associated with defense and metabolism pathways, as well as temporal transcriptional accumulation patterns. Noticeably, the expression levels of resistance-related genes encoding receptor-like kinases/proteins, resistance proteins, mitogen-activated protein kinases (MAPKs), transcription factors, pathogenesis-related proteins, and transport proteins were significantly affected by SCR96. Quantitative reverse transcription PCR (qRT-PCR) validated the transcript changes in the 12 selected genes. Our analysis provides novel information that can help delineate the molecular mechanism and components of plant responses to effectors, which will be useful for the development of resistant crops.
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页数:19
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