Abstract

BackgroundThe hemibiotroph Colletotrichum lentis, causative agent of anthracnose on Lens culinaris (lentil) was recently described as a new species. During its interaction with the host plant, C. lentis likely secretes numerous effector proteins, including toxins to alter the plant’s innate immunity, thereby gaining access to the host tissues for nutrition and reproduction.ResultsIn silico analysis of 2000 ESTs generated from C. lentis-infected lentil leaf tissues identified 15 candidate effectors. In planta infection stage-specific gene expression waves among candidate effectors were revealed for the appressorial penetration phase, biotrophic phase and necrotrophic phase. No sign of positive selection pressure [ω (dN/dS) < 1] in effectors was detected at the intraspecific level. A single nucleotide polymorphism in the ORF of candidate effector ClCE6, used to develop a KASPar marker, differentiated perfectly between pathogenic race 0 and race 1 isolates when tested on 52 isolates arbitrarily selected from a large culture collection representing the western Canadian population of C. lentis. Furthermore, an EST encoding argininosuccinate lyase (Arg) was identified as a bacterial gene. A toxin protein ClToxB was further characterized as a potential host-specific toxin through heterologous in planta expression. The knock-down of ClToxB transcripts by RNAi resulted in reduced virulence, suggesting that ClToxB is a virulence factor. In silico analysis of the ClToxB sequence and comparative genomics revealed that ToxB is unlikely a foreign gene in the C. lentis genome. Incongruency between established species relationships and that established based on gene sequence data confirmed ToxB arose through evolution from a common ancestor, whereas the bacterial gene Arg identified in C. lentis was horizontally transferred from bacteria.ConclusionsEST mining and expression profiling revealed a set of in planta expressed candidate effectors. We developed a KASPar assay using effector polymorphism to differentiate C. lentis races. Comparative genomics revealed a foreign gene encoding a potential virulence factor Arg, which was horizontally transferred from bacteria into the genus Colletotrichum. ClToxB is further characterized as a host-specific toxin that is likely to contribute to quantitative differences in virulence between the races 0 and 1.Electronic supplementary materialThe online version of this article (doi:10.1186/s12864-015-1836-2) contains supplementary material, which is available to authorized users.

Highlights

  • The hemibiotroph Colletotrichum lentis, causative agent of anthracnose on Lens culinaris was recently described as a new species

  • Identification of C. lentis candidate effectors In a previous study, we constructed a directional cDNA plasmid library from Eston leaf tissues infected with C. lentis isolate CT-21 undergoing the morphogenetic biotrophy-necrotrophy transition [5]

  • We identified 15 candidate effectors of C. lentis mined from the biotrophy-necrotrophy switch-specific cDNA library developed previously with the objective to identify effectors that may be involved in the virulence of C. lentis on its host lentil, and may differentiate between the two pathogenic races described in the western Canadian population of this pathogen

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Summary

Introduction

The hemibiotroph Colletotrichum lentis, causative agent of anthracnose on Lens culinaris (lentil) was recently described as a new species. Recent evidence suggests that isolates from several of these hosts were misclassified [2, 3], and Colletotrichum isolates from lentil (Lens culinaris Medik.) were re-classified as C. lentis Damm as part of the destructivum clade [4]. This pathogen initiates infection through single-celled conidia that attach to the aerial parts of the host plants, and germinate to form appressoria instrumental in the mechanical breaching of the host surface.

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