Kooman-Gersmann M, Vogelsang R, Hoogendijk E C, De Wit P J
Department of Phytopathology, Wageningen Agricultural University, The Netherlands.
Mol Plant Microbe Interact. 1997 Sep;10(7):821-9. doi: 10.1094/MPMI.1997.10.7.821.
The AVR9 peptide of Cladosporium fulvum is an elicitor of the hypersensitive response in tomato plants carrying the Cf-9 resistance gene (MM-Cf9). To determine the structure-activity relationship of the AVR9 peptide, amino acids important for AVR9 elicitor activity were identified by independently substituting each amino acid of AVR9 by alanine. In addition, surface-exposed amino acid residues of AVR9 were substituted by other amino acids. Activity of the mutant Avr9 constructs was studied by expressing the constructs in MM-Cf9 tomato plants, using the potato virus X (PVX) expression system and assessing the severity of necrosis induced by each PVX::Avr9 construct. This allowed direct identification of amino acid residues of AVR9 that are essential for elicitor activity. We identified amino acid substitutions that resulted in AVR9 mutants with higher, similar, or lower elicitor activity compared to the wild-type AVR9 peptide. Some mutants had completely lost elicitor activity. A selection of peptides, representing different categories, was isolated and injected into leaves of MM-Cf9 plants. The necrosis-inducing activity of the isolated peptides correlated well with the necrosis induced by the corresponding PVX::Avr9 derivatives. Based on the necrosis-inducing activity of the mutant AVR9 peptides and the global structure of AVR9, we assigned sites in AVR9 that are important for its necrosis-inducing activity. We postulate that the "hydrophobic beta-loop" region of the AVR9 peptide is crucial for necrosis-inducing activity in tomato plants that carry the Cf-9 resistance gene.
番茄叶霉病菌的AVR9肽是携带Cf-9抗性基因(MM-Cf9)的番茄植株中超敏反应的激发子。为了确定AVR9肽的构效关系,通过将AVR9的每个氨基酸独立替换为丙氨酸,鉴定了对AVR9激发子活性重要的氨基酸。此外,AVR9表面暴露的氨基酸残基被其他氨基酸取代。利用马铃薯X病毒(PVX)表达系统,在MM-Cf9番茄植株中表达突变的Avr9构建体,并评估每个PVX::Avr9构建体诱导坏死的严重程度,研究了突变体Avr9构建体的活性。这使得能够直接鉴定AVR9中对激发子活性至关重要的氨基酸残基。我们鉴定出了与野生型AVR9肽相比,具有更高、相似或更低激发子活性的AVR9突变体的氨基酸取代。一些突变体完全丧失了激发子活性。分离出代表不同类别的一组肽,并将其注射到MM-Cf9植株的叶片中。分离出的肽的坏死诱导活性与相应的PVX::Avr9衍生物诱导的坏死密切相关。基于突变的AVR9肽的坏死诱导活性和AVR9的整体结构,我们确定了AVR9中对其坏死诱导活性重要的位点。我们推测,AVR9肽的“疏水β-环”区域对于携带Cf-9抗性基因的番茄植株中的坏死诱导活性至关重要。