Conserved genetic defense response against X. fastidiosa subsp. pauca in olive and citrus

Abstract

X. fastidiosa subsp. pauca causes diseases in citrus and olive plants. Fortunately, there are citrus species and olive varieties more tolerant to X. fastidiosa and therefore good genotypes to search for genetic sources of resistance. Following this approach, global gene expression analyses were recently achieved using Citrus reticulata cv. Ponkan and Olea europaea cv. Leccino allowing the identification of potential genes involved in plant defense response. Thus, the objective of this work was to identify key genes involved in common genetic defense responses that could be further explored to get resistant varieties. Overall we identified two main mechanisms for both plant species: i. Bacteria recognition and ii. Cell wall fortification. The former involve the expression of patternrecognition receptors, which recognize pathogen molecular patterns and trigger cell defense responses. Some of these receptors belong to the LRR-XII group which contains cell surface immune receptors. The latter involves downregulation of genes in tolerant host such as expansin, pectate lyases and polygalacturonases, related with cell wall expansion and degradation. This suggests that in tolerant hosts, plant cell recognizes X. fastidiosa and reprograms the cell wall development to impair its colonization through the xylem vessels. Therefore these genes represent good candidates to be explored aiming their use in breeding and/or genetic engineering program. Giampetruzzi A., Morelli M., Saponari M., Loconsole G., Chiumenti M., Boscia D., Savino V.N., Martelli G.P. & Saldarelli P. 2016. Transcriptome profiling of two olive cultivars in response to infection by the CoDiRO strain of Xylella fastidiosa subsp. pauca. BMC Genomics 17:475. Rodrigues C.M., De Souza A.A., Takita M.A., Kishi L.T. & Machado M.A. 2013. RNA-Seq analysis of Citrus reticulata in the early stages of Xylella fastidiosa infection reveals auxin-related genes as a defense response. BMC Genomics 14: 676

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