Browse Articles

Article|24 Sep 2014|OPEN
Transcriptome of Erysiphe necator-infected Vitis pseudoreticulata leaves provides insight into grapevine resistance to powdery mildew
Kai Weng1,2,3 , Zhi-Qian Li1,2,4 , Lan Wang1,2,4 , Yue-Jin Wang1,2,4 , Yan Xu,1,2,4 ,
1State Key Laboratory of Crop Stress Biology in Arid Areas (Northwest A&F University), Yangling, shanxi 712100, China
2College of Horticulture, Northwest A&F University, Yangling, shanxi 712100, China
3Key Laboratory of Horticultural Plant Biology and Germplasm Innovation in Northwest China, Ministry of Agriculture, Yangling, shanxi 712100, China.
4Key Laboratory of Horticultural Plant Biology and Germplasm Innovation in Northwest China, Ministry of Agriculture, Yangling, shanxi 712100, China
*Corresponding author. E-mail: yan.xu@nwsuaf.edu.cn

Horticulture Research 1,
Article number: 47 (2014)
doi: https://doi.org/10.1038/hortres.2014.49
Views: 988

Received: 20 Jun 2014
Revised: 11 Jul 2014
Accepted: 06 Aug 2014
Published online: 24 Sep 2014

Abstract

Powdery mildew (PM), which is caused by the pathogen Erysiphe necator (Schw.) Burr., is the single most damaging disease of cultivated grapes (Vitis vinifera) worldwide. However, little is known about the transcriptional response of grapes to infection with PM. RNA-seq analysis was used for deep sequencing of the leaf transcriptome to study PM resistance in Chinese wild grapes (V. pseudoreticulata Baihe 35-1) to better understand the interaction between host and pathogen. Greater than 100 million (M) 90-nt cDNA reads were sequenced from a cDNA library derived from PM-infected leaves. Among the sequences obtained, 6541 genes were differentially expressed (DEG) and were annotated with Gene Ontology terms and by pathway enrichment. The significant categories that were identified included the following: defense, salicylic acid (SA) and jasmonic acid (JA) responses; systemic acquired resistance (SAR); hypersensitive response; plant–pathogen interaction; flavonoid biosynthesis; and plant hormone signal transduction. Various putative secretory proteins were identified, indicating potential defense responses to PM infection. In all, 318 putative R-genes and 183 putative secreted proteins were identified, including the defense-related R-genes BAK1, MRH1 and MLO3 and the defense-related secreted proteins GLP and PR5. The expression patterns of 16 genes were further illuminated by RT-qPCR. The present study identified several candidate genes and pathways that may contribute to PM resistance in grapes and illustrated that RNA-seq is a powerful tool for studying gene expression. The RT-qPCR results reveal that effective resistance responses of grapes to PM include enhancement of JA and SAR responses and accumulation of phytoalexins.