Botrytis hypersensitive response inducing protein 1 triggers noncanonical PTI to induce plant cell death

被引:19
|
作者
Jeblick, Tanja [1 ]
Leisen, Thomas [1 ]
Steidele, Christina E. [2 ]
Albert, Isabell [3 ]
Mueller, Jonas [1 ]
Kaiser, Sabrina [1 ]
Mahler, Florian [4 ]
Sommer, Frederik [5 ]
Keller, Sandro [4 ,6 ,7 ,8 ]
Hueckelhoven, Ralph [2 ]
Hahn, Matthias [1 ]
Scheuring, David [1 ]
机构
[1] Univ Kaiserslautern, Plant Pathol, D-67663 Kaiserslautern, Germany
[2] Tech Univ Munich, TUM Sch Life Sci, Phytopathol, D-85354 Freising Weihenstephan, Germany
[3] FAU Erlangen, Mol Plant Physiol, D-91058 Erlangen, Germany
[4] Univ Kaiserslautern, Mol Biophys, D-67663 Kaiserslautern, Germany
[5] Univ Kaiserslautern, Mol Biotechnol & Syst Biol, D-67663 Kaiserslautern, Germany
[6] Karl Franzens Univ Graz, Inst Mol Biosci IMB, NAWI Graz, Biophys, A-8010 Graz, Austria
[7] Karl Franzens Univ Graz, Field Excellence BioHlth, Graz, Austria
[8] BioTechMed Graz, Graz, Austria
关键词
PHYTOTOXIC NEP1-LIKE PROTEINS; PARASITICA VAR.-NICOTIANAE; ARABIDOPSIS-THALIANA; RICH PROTEIN; CINEREA; VIRULENCE; ELICITOR; DEFENSE; ENDOPOLYGALACTURONASES; RECOGNITION;
D O I
10.1093/plphys/kiac476
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The secreted Botrytis protein hypersensitive response inducing protein 1 activates plant defense to kill plant cells. According to their lifestyle, plant pathogens are divided into biotrophic and necrotrophic organisms. Biotrophic pathogens exclusively nourish living host cells, whereas necrotrophic pathogens rapidly kill host cells and nourish cell walls and cell contents. To this end, the necrotrophic fungus Botrytis cinerea secretes large amounts of phytotoxic proteins and cell wall-degrading enzymes. However, the precise role of these proteins during infection is unknown. Here, we report on the identification and characterization of the previously unknown toxic protein hypersensitive response-inducing protein 1 (Hip1), which induces plant cell death. We found the adoption of a structurally conserved folded Alternaria alternata Alt a 1 protein structure to be a prerequisite for Hip1 to exert its necrosis-inducing activity in a host-specific manner. Localization and the induction of typical plant defense responses by Hip1 indicate recognition as a pathogen-associated molecular pattern at the plant plasma membrane. In contrast to other secreted toxic Botrytis proteins, the activity of Hip1 does not depend on the presence of the receptor-associated kinases BRI1-associated kinase 1 and suppressor of BIR1-1. Our results demonstrate that recognition of Hip1, even in the absence of obvious enzymatic or pore-forming activity, induces strong plant defense reactions eventually leading to plant cell death. Botrytis hip1 overexpression strains generated by CRISPR/Cas9 displayed enhanced infection, indicating the virulence-promoting potential of Hip1. Taken together, Hip1 induces a noncanonical defense response which might be a common feature of structurally conserved fungal proteins from the Alt a 1 family.
引用
收藏
页码:125 / 141
页数:17
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