1. Subcellular Localization Screening of Colletotrichum higginsianum Effector Candidates Identifies Fungal Proteins Targeted to Plant Peroxisomes, Golgi Bodies, and Microtubules
- Author
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Nicolas Lapalu, Jean-Félix Dallery, Ulla Neumann, Richard J. O'Connell, Lisa Cabre, Jochen Kleemann, Guillaume P. Robin, BIOlogie et GEstion des Risques en agriculture (BIOGER), Institut National de la Recherche Agronomique (INRA)-AgroParisTech, Université Paris Saclay (COmUE), Max-Planck-Institut, Bayer Pharma AG [Berlin], Max Planck Inst Plant Breeding Res, Cent Microscopy, Cologne, Germany, Partenaires INRAE, Bayer SAS, Agence Nationale de la Recherche [ANR-12-CHEX-0008-01], and Deutsche Forschungsgemeinschaft [SPP1212, OC104/1-3]
- Subjects
0301 basic medicine ,[SDV]Life Sciences [q-bio] ,Plant Science ,lcsh:Plant culture ,Biology ,Peroxisome localization ,localization ,microtubules ,03 medical and health sciences ,symbols.namesake ,Colletotrichum ,Golgi ,lcsh:SB1-1110 ,peroxisome ,Colletotrichum higginsianum ,Original Research ,Fungal protein ,Effector ,Peroxisomal Targeting Signal 1 ,effectoromics ,fungi ,fungus ,nucleus ,food and beverages ,Golgi apparatus ,Subcellular localization ,biology.organism_classification ,Cell biology ,030104 developmental biology ,[SDE]Environmental Sciences ,symbols ,Cortical microtubule - Abstract
International audience; The genome of the hemibiotrophic anthracnose fungus, Colletotrichum higginsianum, encodes a large inventory of putative secreted effector proteins that are sequentially expressed at different stages of plant infection, namely appressorium-mediated penetration, biotrophy and necrotrophy. However, the destinations to which these proteins are addressed inside plant cells are unknown. In the present study, we selected 61 putative effector genes that are highly induced in appressoria and/or biotrophic hyphae. We then used Agrobacterium-mediated transformation to transiently express them as N-terminal fusions with fluorescent proteins in cells of Nicotiana benthamiana for imaging by confocal microscopy. Plant compartments labeled by the fusion proteins in N. benthamiana were validated by co-localization with specific organelle markers, by transient expression of the proteins in the true host plant, Arabidopsis thaliana, and by transmission electron microscopy-immunogold labeling. Among those proteins for which specific subcellular localizations could be verified, nine were imported into plant nuclei, three were imported into the matrix of peroxisomes, three decorated cortical microtubule arrays and one labeled Golgi stacks. Two peroxisome-targeted proteins harbored canonical C-terminal tripeptide signals for peroxisome import via the PTS1 (peroxisomal targeting signal 1) pathway, and we showed that these signals are essential for their peroxisome localization. Our findings provide valuable information about which host processes are potentially manipulated by this pathogen, and also reveal plant peroxisomes, microtubules, and Golgi as novel targets for fungal effectors.
- Published
- 2018
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