Abstract

BackgroundTrunk diseases threaten the longevity and productivity of grapevines in all viticulture production systems. They are caused by distantly-related fungi that form chronic wood infections. Variation in wood-decay abilities and production of phytotoxic compounds are thought to contribute to their unique disease symptoms. We recently released the draft sequences of Eutypa lata, Neofusicoccum parvum and Togninia minima, causal agents of Eutypa dieback, Botryosphaeria dieback and Esca, respectively. In this work, we first expanded genomic resources to three important trunk pathogens, Diaporthe ampelina, Diplodia seriata, and Phaeomoniella chlamydospora, causal agents of Phomopsis dieback, Botryosphaeria dieback, and Esca, respectively. Then we integrated all currently-available information into a genome-wide comparative study to identify gene families potentially associated with host colonization and disease development.ResultsThe integration of RNA-seq, comparative and ab initio approaches improved the protein-coding gene prediction in T. minima, whereas shotgun sequencing yielded nearly complete genome drafts of Dia. ampelina, Dip. seriata, and P. chlamydospora. The predicted proteomes of all sequenced trunk pathogens were annotated with a focus on functions likely associated with pathogenesis and virulence, namely (i) wood degradation, (ii) nutrient uptake, and (iii) toxin production. Specific patterns of gene family expansion were described using Computational Analysis of gene Family Evolution, which revealed lineage-specific evolution of distinct mechanisms of virulence, such as specific cell wall oxidative functions and secondary metabolic pathways in N. parvum, Dia. ampelina, and E. lata. Phylogenetically-informed principal component analysis revealed more similar repertoires of expanded functions among species that cause similar symptoms, which in some cases did not reflect phylogenetic relationships, thereby suggesting patterns of convergent evolution.ConclusionsThis study describes the repertoires of putative virulence functions in the genomes of ubiquitous grapevine trunk pathogens. Gene families with significantly faster rates of gene gain can now provide a basis for further studies of in planta gene expression, diversity by genome re-sequencing, and targeted reverse genetic approaches. The functional validation of potential virulence factors will lead to a more comprehensive understanding of the mechanisms of pathogenesis and virulence, which ultimately will enable the development of accurate diagnostic tools and effective disease management.Electronic supplementary materialThe online version of this article (doi:10.1186/s12864-015-1624-z) contains supplementary material, which is available to authorized users.

Highlights

  • Trunk diseases threaten the longevity and productivity of grapevines in all viticulture production systems

  • This study describes the repertoires of putative virulence functions in the genomes of ubiquitous grapevine trunk pathogens

  • Core Eukaryotic Genes Mapping Approach (CEGMA) [40] and tRNA analyses indicated a high degree of completeness of the assembled gene space (Table 2; Additional file 2: Table S1; Additional file 3: Table S2)

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Summary

Introduction

Trunk diseases threaten the longevity and productivity of grapevines in all viticulture production systems. We first expanded genomic resources to three important trunk pathogens, Diaporthe ampelina, Diplodia seriata, and Phaeomoniella chlamydospora, causal agents of Phomopsis dieback, Botryosphaeria dieback, and Esca, respectively. Botryosphaeria dieback, Phomopsis dieback, and Esca are the most important trunk diseases of grapevines (Vitis vinifera L.). They are common in vineyards worldwide, where they are responsible for significant reductions in productivity and longevity [1,2,3,4,5]. Once a vine is infected, the only means of eradicating a trunk pathogen is by physically cutting out infected tissues and retraining new vines As vines age, they accumulate wood cankers and yield

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