Abstract

Anthracnose causes severe losses of tea production in China. Although genes and biological processes involved in anthracnose resistance have been reported in other plants, the molecular response to anthracnose in tea plant is unknown. We used the susceptible tea cultivar Longjing 43 and the resistant cultivar Zhongcha 108 as materials and compared transcriptome changes in the leaves of both cultivars following Colletotrichum fructicola inoculation. In all, 9015 and 8624 genes were differentially expressed between the resistant and susceptible cultivars and their controls (0 h), respectively. In both cultivars, the differentially expressed genes (DEGs) were enriched in 215 pathways, including responses to sugar metabolism, phytohormones, reactive oxygen species (ROS), biotic stimuli and signalling, transmembrane transporter activity, protease activity and signalling receptor activity, but DEG expression levels were higher in Zhongcha 108 than in Longjing 43. Moreover, functional enrichment analysis of the DEGs showed that hydrogen peroxide (H2O2) metabolism, cell death, secondary metabolism, and carbohydrate metabolism are involved in the defence of Zhongcha 108, and 88 key genes were identified. Protein–protein interaction (PPI) network demonstrated that putative mitogen-activated protein kinase (MAPK) cascades are activated by resistance (R) genes and mediate downstream defence responses. Histochemical analysis subsequently validated the strong hypersensitive response (HR) and H2O2 accumulation that occurred around the hyphal infection sites in Zhongcha 108. Overall, our results indicate that the HR and H2O2 are critical mechanisms in tea plant defence against anthracnose and may be activated by R genes via MAPK cascades.

Highlights

  • The results of the Gene Ontology (GO) analysis demonstrated that programmed cell death (PCD) was a defensive pathway that contained enriched differentially expressed genes (DEGs) in the resistant cultivar (Fig. 3c), and microscopic observations showed that the hypersensitive response (HR) significantly accumulated around the C. fructicola hyphal infection site in the resistant tea plant cultivar (Fig. 6)

  • We suggested that H2O2 plays a significant role in tea plant defence to C. fructicola, H2O2 generation may be directed by peroxin 11a (PEX11a) under pathogen stress and mediated by mitogen-activated protein kinase (MAPK) cascades, and peroxidase 2 (PA2) may be inhibited by other genes to maintain higher levels of H2O2 in tea plant to defend against C. fructicola

  • We previously demonstrated that the content of (-)-epigallocatechin-3gallate and caffeine rapidly accumulated after C. fructicola infection; at the same time, the expression levels of key genes associated with flavonoids and the caffeine metabolism pathway were clearly upregulated, including the phenylalanine ammonia-lyase (PAL) and S-adenosylmethionine synthetase (SAMS)[4]

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Summary

Introduction

As an important commercial product, the fresh shoots of tea plant provide an wide variety of nutrition for the human body, including flavonoids, alkaloids and theanine. Long-term tea drinking can protect against different diseases; tea has become the most popular healthy, non-alcoholic beverage in the world[1,2]. Tea plant is frequently affected by many kinds of disease. Of these diseases, anthracnose, Wang et al Horticulture Research (2018)5:18 which is caused by Colletotrichum, is one of the most devastating diseases to tea plant[3]. Colletotrichum damages mature tea plant leaves, affecting the growth and yield of the plant[4]

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