Abstract

Virus infection of plants can result in various degrees of detrimental impacts and disparate symptom types and severities. Although great strides have been made in our understanding of the virus–host interactions in herbaceous model plants, the mechanisms underlying symptom development are poorly understood in perennial fruit crops. Grapevine fanleaf virus (GFLV) causes variable symptoms in most vineyards worldwide. To better understand GFLV-grapevine interactions in relation to symptom development, field and greenhouse trials were conducted with a grapevine genotype that exhibits distinct symptoms in response to a severe and a mild strain of GFLV. After validation of the infection status of the experimental vines by high-throughput sequencing, the transcriptomic and metabolomic profiles in plants infected with the two viral strains were tested and compared by RNA-Seq and LC-MS, respectively, in the differentiating grapevine genotype. In vines infected with the severe GFLV strain, 1023 genes, among which some are implicated in the regulation of the hypersensitive-type response, were specifically deregulated, and a higher accumulation of resveratrol and phytohormones was observed. Interestingly, some experimental vines restricted the virus to the rootstock and remained symptomless. Our results suggest that GFLV induces a strain- and cultivar-specific defense reaction similar to a hypersensitive reaction. This type of defense leads to a severe stunting phenotype in some grapevines, whereas others are resistant. This work is the first evidence of a hypersensitive-like reaction in grapevine during virus infection.

Highlights

  • The development of severe symptoms, rather than the presence of the virus itself, constitutes the main nuisance caused by viral infections in crop plants

  • We showed that a hypersensitive reaction (HR) is responsible for necrotic symptoms induced by grapevine fanleaf virus (GFLV) strain F13 in N. occidentalis and identified protein 2A as the avirulence factor

  • This has provided the tools to compare the transcriptome of plants infected by a severe (B844), and a mild strain (F13), of GFLV in order to shed light on the mechanisms underlying pathogenesis

Read more

Summary

Introduction

The development of severe symptoms, rather than the presence of the virus itself, constitutes the main nuisance caused by viral infections in crop plants. It is generally accepted that virus–host interactions are responsible for the development of symptoms, rather than the competition for resources [1,2,3,4]. These specific interactions between the viral pathogenicity determinants and the host components are thought to perturbate the host physiology [3]. While many viral pathogenicity factors, and their mutants, affecting symptom severity have been identified [12,13,14,15,16,17,18,19,20,21,22], examples of the interactant host factors are rare and, more importantly, the underlying mechanisms have not been described [10,23,24,25]. Virus–host studies have essentially been conducted on model plants of the genus Arabidopsis [23] or Nicotiana [10,24,25]

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call