Dual RNA‐seq reveals Meloidogyne graminicola transcriptome and candidate effectors during the interaction with rice plants. (4th April 2016)

• Record Type: Journal Article
• Authors: Petitot, Anne‐Sophie; Dereeper, Alexis; Agbessi, Mawusse; Da Silva, Corinne; Guy, Julie; Ardisson, Morgane; Fernandez, Diana
• Is Part Of: Molecular plant pathology. Volume 17:Number 6(2016:Aug.)
• Page Start: 860
• Page End: 874
• Publication Date: 2016-04-04
• Subjects: dual RNA‐seq -- effector genes -- expression profiling -- Meloidogyne graminicola -- Oryza sativa -- plant‐parasitic nematode; Plant diseases -- Molecular aspects -- Periodicals; Plant-pathogen relationships -- Molecular aspects -- Periodicals; 571.936
• DOI: 10.1111/mpp.12334
• Languages: English
• ISSNs: 1464-6722

Abstract

Summary: Root‐knot nematodes secrete proteinaceous effectors into plant tissues to facilitate infection by suppressing host defences and reprogramming the host metabolism to their benefit. Meloidogyne graminicola is a major pest of rice ( Oryza sativa ) in Asia and Latin America, causing important crop losses. The goal of this study was to identify M. graminicola pathogenicity genes expressed during the plant–nematode interaction. Using the dual RNA‐sequencing (RNA‐seq) strategy, we generated transcriptomic data of M. graminicola samples covering the pre‐parasitic J2 stage and five parasitic stages in rice plants, from the parasitic J2 to the adult female. In the absence of a reference genome, a de novo M. graminicola transcriptome of 66 396 contigs was obtained from those reads that were not mapped on the rice genome. Gene expression profiling across the M. graminicola life cycle revealed key genes involved in nematode development and provided insights into the genes putatively associated with parasitism. The development of a 'secreted protein prediction' pipeline revealed a typical set of proteins secreted by nematodes, as well as a large number of cysteine‐rich proteins and putative nuclear proteins. Combined with expression data, this pipeline enabled the identification of 15 putative effector genes, including two homologues of well‐characterized effectors from cyst nematodes (CLE‐like and VAP1) and a metallothionein. The localization of gene expression was assessed by in situ hybridization for a subset of candidates. All of these data represent important molecular resources for the elucidation of M. graminicola biology and for the selection of potential targets for the development of novel control strategies for this nematode species.