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- W2956455508 endingPage "e1007747" @default.
- W2956455508 startingPage "e1007747" @default.
- W2956455508 abstract "The intracellular accommodation structures formed by plant cells to host arbuscular mycorrhiza fungi and biotrophic hyphal pathogens are cytologically similar. Therefore we investigated whether these interactions build on an overlapping genetic framework. In legumes, the malectin-like domain leucine-rich repeat receptor kinase SYMRK, the cation channel POLLUX and members of the nuclear pore NUP107-160 subcomplex are essential for symbiotic signal transduction and arbuscular mycorrhiza development. We identified members of these three groups in Arabidopsis thaliana and explored their impact on the interaction with the oomycete downy mildew pathogen Hyaloperonospora arabidopsidis (Hpa). We report that mutations in the corresponding genes reduced the reproductive success of Hpa as determined by sporangiophore and spore counts. We discovered that a developmental transition of haustorial shape occurred significantly earlier and at higher frequency in the mutants. Analysis of the multiplication of extracellular bacterial pathogens, Hpa-induced cell death or callose accumulation, as well as Hpa- or flg22-induced defence marker gene expression, did not reveal any traces of constitutive or exacerbated defence responses. These findings point towards an overlap between the plant genetic toolboxes involved in the interaction with biotrophic intracellular hyphal symbionts and pathogens in terms of the gene families involved." @default.
- W2956455508 created "2019-07-23" @default.
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- W2956455508 date "2019-07-12" @default.
- W2956455508 modified "2023-10-06" @default.
- W2956455508 title "A set of Arabidopsis genes involved in the accommodation of the downy mildew pathogen Hyaloperonospora arabidopsidis" @default.
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- W2956455508 doi "https://doi.org/10.1371/journal.ppat.1007747" @default.
- W2956455508 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6625732" @default.
- W2956455508 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/31299058" @default.
- W2956455508 hasPublicationYear "2019" @default.