The strong association between Phytophthora cinnamomi and the mortality and decline of Quercus suber and Q. ilex subsp. rotundifolia has been known for two decades. The ability of elicitins secreted by this pathogen to trigger defence responses in these Quercus against itself was evaluated in this work. Biomass quantification by quantitative real-time PCR revealed a significant decrease in pathogen colonization of Q. suber roots after 24 h pre-treatment with α-and β-cinnamomin. In Q. suber and Q. ilex roots pre-treated with α-cinnamomin, hyphae were unable to reach and colonize the vascular cylinder and showed cytoplasmic disorganization in all the roots observed as contrasted with non-pre-treated roots. The pathogen was restricted to the intercellular spaces of the cortical parenchyma and the concomitant accumulation of electron dense materials was observed in contact with the hyphae. Furthermore, ROS (reactive oxygen species) production and the enzymatic activities of superoxide dismutase, catalase and peroxidase were compared in infected and non-infected Quercus roots in time course trials. There was a significant increase in the production of hydrogen peroxide (H2O2) and superoxide anion (O •-) and an enhanced activity of the enzymes in infected roots was observed at each time point. When comparing with elicitin non-treated roots, the α-cinnamomin-treated roots in interaction with P. cinnamomi showed a decrease in ROS accumulation and an increase of the enzyme activities. The overall results were consistent with an induction by the cinnamomins which initiated defence responses against the pathogen invasion of roots. Finally, elicitins were immunolocalized in the contact zone of P. cinnamomi hyphae with epidermal host cells, plasmalemma outer cytoplasm and around the intracellular hyphae in the vacuoles of invaded epidermal cells.

cDNA-AFLP methodology was used to gain insight into gene fragments differentially present in the mRNA profiles of Quercus suber roots infected with zoospores of Phytophthora cinnamomi at different post challenge time points. Fifty-three transcript-derived fragments (TDFs) were identified and sequenced. Six candidate genes were selected based on their expression patterns and homology to genes known to play a role in defence. They encode a cinnamyl alcohol dehydrogenase2 (QsCAD2), a protein disulphide isomerase (QsPDI), a CC-NBS-LRR resistance protein (QsRPc), a thaumatin-like protein (QsTLP), a chitinase (QsCHI) and a 1,3-β-glucanase (QsGlu). Evaluation of the expression of these genes by quantitative polymerase chain reaction (qPCR) revealed that transcript levels of QsRPc, QsCHI, QsCAD2 and QsPDI increased during the first 24 h post-inoculation, while those of thaumatin-like protein decreased. No differential expression was observed for 1,3-β-glucanase (QsGlu).Four candidate reference genes, polymerase II (QsRPII), eukaryotic translation initiation factor 5A (QsEIF-5A), β-tubulin (QsTUB) and a medium subunit family protein of clathrin adaptor complexes (QsCACs) were assessed to determine the most stable internal references for qRT-PCR normalization in the Phytophthora-Q. suber pathosystem in root tissues. Those found to be more stable, QsRPII and QsCACs, were used as internal reference in the present work.Knowledge on the Quercus defence mechanisms against biotic stress is scarce. This study provides an insight into the gene profiling of a few important genes of Q. suber in response to P. cinnamomi infection contributing to the knowledge of the molecular interactions involving Quercus and root pathogens that can be useful in the future to understand the mechanisms underlying oak resistance to soil-borne oomycetes.Electronic supplementary materialThe online version of this article (doi:10.1186/2193-1801-3-613) contains supplementary material, which is available to authorized users.