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      Conserved fungal effector suppresses PAMP-triggered immunity by targeting plant immune kinases

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          Significance

          Multiple effectors of bacterial pathogens target immune kinases such as BAK1 and BIK1, but it is unclear whether this strategy is employed by fungal pathogens. We reveal here that a fungal effector named NIS1 is broadly conserved in filamentous fungi in the Ascomycota and Basidiomycota, thus being regarded as a core effector, and has the ability to suppress PAMP-triggered immunity. Importantly, NIS1 targets BAK1 and BIK1, interfering with their essential functions for immune activation upon pathogen recognition. Multifaceted analyses including the knockout of NIS1 revealed that it plays a critical role in fungal infection. These findings demonstrate that to infect host plants, filamentous fungi deploy a core effector that attacks conserved immune kinases critical for the ancestral defense system.

          Abstract

          Plant pathogens have optimized their own effector sets to adapt to their hosts. However, certain effectors, regarded as core effectors, are conserved among various pathogens, and may therefore play an important and common role in pathogen virulence. We report here that the widely distributed fungal effector NIS1 targets host immune components that transmit signaling from pattern recognition receptors (PRRs) in plants. NIS1 from two Colletotrichum spp. suppressed the hypersensitive response and oxidative burst, both of which are induced by pathogen-derived molecules, in Nicotiana benthamiana. Magnaporthe oryzae NIS1 also suppressed the two defense responses, although this pathogen likely acquired the NIS1 gene via horizontal transfer from Basidiomycota. Interestingly, the root endophyte Colletotrichum tofieldiae also possesses a NIS1 homolog that can suppress the oxidative burst in N. benthamiana. We show that NIS1 of multiple pathogens commonly interacts with the PRR-associated kinases BAK1 and BIK1, thereby inhibiting their kinase activities and the BIK1-NADPH oxidase interaction. Furthermore, mutations in the NIS1-targeting proteins, i.e., BAK1 and BIK1, in Arabidopsis thaliana also resulted in reduced immunity to Colletotrichum fungi. Finally, M. oryzae lacking NIS1 displayed significantly reduced virulence on rice and barley, its hosts. Our study therefore reveals that a broad range of filamentous fungi maintain and utilize the core effector NIS1 to establish infection in their host plants and perhaps also beneficial interactions, by targeting conserved and central PRR-associated kinases that are also known to be targeted by bacterial effectors.

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          Most cited references51

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          ETE 3: Reconstruction, Analysis, and Visualization of Phylogenomic Data

          The Environment for Tree Exploration (ETE) is a computational framework that simplifies the reconstruction, analysis, and visualization of phylogenetic trees and multiple sequence alignments. Here, we present ETE v3, featuring numerous improvements in the underlying library of methods, and providing a novel set of standalone tools to perform common tasks in comparative genomics and phylogenetics. The new features include (i) building gene-based and supermatrix-based phylogenies using a single command, (ii) testing and visualizing evolutionary models, (iii) calculating distances between trees of different size or including duplications, and (iv) providing seamless integration with the NCBI taxonomy database. ETE is freely available at http://etetoolkit.org
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            A flagellin-induced complex of the receptor FLS2 and BAK1 initiates plant defence.

            Plants sense potential microbial invaders by using pattern-recognition receptors to recognize pathogen-associated molecular patterns (PAMPs). In Arabidopsis thaliana, the leucine-rich repeat receptor kinases flagellin-sensitive 2 (FLS2) (ref. 2) and elongation factor Tu receptor (EFR) (ref. 3) act as pattern-recognition receptors for the bacterial PAMPs flagellin and elongation factor Tu (EF-Tu) (ref. 5) and contribute to resistance against bacterial pathogens. Little is known about the molecular mechanisms that link receptor activation to intracellular signal transduction. Here we show that BAK1 (BRI1-associated receptor kinase 1), a leucine-rich repeat receptor-like kinase that has been reported to regulate the brassinosteroid receptor BRI1 (refs 6,7), is involved in signalling by FLS2 and EFR. Plants carrying bak1 mutations show normal flagellin binding but abnormal early and late flagellin-triggered responses, indicating that BAK1 acts as a positive regulator in signalling. The bak1-mutant plants also show a reduction in early, but not late, EF-Tu-triggered responses. The decrease in responses to PAMPs is not due to reduced sensitivity to brassinosteroids. We provide evidence that FLS2 and BAK1 form a complex in vivo, in a specific ligand-dependent manner, within the first minutes of stimulation with flagellin. Thus, BAK1 is not only associated with developmental regulation through the plant hormone receptor BRI1 (refs 6,7), but also has a functional role in PRR-dependent signalling, which initiates innate immunity.
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              Regulation of pattern recognition receptor signalling in plants.

              Recognition of pathogen-derived molecules by pattern recognition receptors (PRRs) is a common feature of both animal and plant innate immune systems. In plants, PRR signalling is initiated at the cell surface by kinase complexes, resulting in the activation of immune responses that ward off microorganisms. However, the activation and amplitude of innate immune responses must be tightly controlled. In this Review, we summarize our knowledge of the early signalling events that follow PRR activation and describe the mechanisms that fine-tune immune signalling to maintain immune homeostasis. We also illustrate the mechanisms used by pathogens to inhibit innate immune signalling and discuss how the innate ability of plant cells to monitor the integrity of key immune components can lead to autoimmune phenotypes following genetic or pathogen-induced perturbations of these components.
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                Author and article information

                Journal
                Proc Natl Acad Sci U S A
                Proc. Natl. Acad. Sci. U.S.A
                pnas
                pnas
                PNAS
                Proceedings of the National Academy of Sciences of the United States of America
                National Academy of Sciences
                0027-8424
                1091-6490
                8 January 2019
                24 December 2018
                24 December 2018
                : 116
                : 2
                : 496-505
                Affiliations
                [1] aGraduate School of Agriculture, Kyoto University , Kyoto 606-8502, Japan;
                [2] bAcademic Assembly, Institute of Agriculture, Shinshu University , Nagano 399-4598, Japan;
                [3] cResearch Institute for Bioresources and Biotechnology, Ishikawa Prefectural University , Ishikawa 921-8836, Japan;
                [4] dGraduate School of Technology, Industrial and Social Sciences, Tokushima University , Tokushima 770-8513, Japan;
                [5] eDepartment of Molecular Microbiology, Tokyo University of Agriculture , Tokyo 156-8502, Japan;
                [6] fIwate Biotechnology Research Center , Iwate 024-0003, Japan
                Author notes
                1To whom correspondence should be addressed. Email: ytakano@ 123456kais.kyoto-u.ac.jp .

                Edited by Paul Schulze-Lefert, Max Planck Institute for Plant Breeding Research, Cologne, Germany, and approved November 21, 2018 (received for review April 27, 2018)

                Author contributions: Y.T. designed research; H.I., Y.I., M.M., K.Y., Y.O., H.S., A.U., S.K., A.K., and S.S.-O. performed research; H.I., Y.I., S.K., A.K., S.S.-O., and Y.T. analyzed data; and H.I., Y.I., M.M., H.S., R.T., and Y.T. wrote the paper.

                Article
                201807297
                10.1073/pnas.1807297116
                6329965
                30584105
                64eee780-cacf-4d4b-b6f9-64797e05b7d9
                Copyright © 2019 the Author(s). Published by PNAS.

                This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND).

                History
                Page count
                Pages: 10
                Funding
                Funded by: MEXT | Japan Society for the Promotion of Science (JSPS) 501100001691
                Award ID: 15H05780
                Award Recipient : Yoshitaka Takano
                Funded by: MEXT | Japan Society for the Promotion of Science (JSPS) 501100001691
                Award ID: 18H02204
                Award Recipient : Yoshitaka Takano
                Categories
                PNAS Plus
                Biological Sciences
                Agricultural Sciences
                PNAS Plus

                bak1,bik1,core effector,pamp-triggered immunity,phytopathogenic fungi

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