综述

植物与病原微生物互作分子基础的研究进展

展开
  • 中国科学院微生物研究所植物基因组学国家重点实验室, 北京 100101

收稿日期: 2011-05-12

  修回日期: 2011-07-27

  网络出版日期: 2012-02-25

基金资助

中国科学院知识创新工程重要方向项目(编号: KSCX2-EW-J-6)资助

Advances on molecular mechanisms of plant-pathogen interactions

Expand
  • State Key Laboratory of Plant Genomics, Institute of Microbiology, Chinese Academy of Science, Beijing 100101, China

Received date: 2011-05-12

  Revised date: 2011-07-27

  Online published: 2012-02-25

摘要

植物在与病原微生物共同进化过程中形成了复杂的免疫防卫体系。植物的先天免疫系统可大致分为两个层面。第一个层面的免疫基于细胞表面的模式识别受体对病原物相关分子模式的识别, 该免疫过程被称为病原物相关分子模式触发的免疫(PAMP-triggered immunity, PTI), 能帮助植物抵抗大部分病原微生物; 第二个层面的免疫起始于细胞内部, 主要依靠抗病基因编码的蛋白产物直接或间接识别病原微生物分泌的效应子并且激发防卫反应, 来抵抗那些能够利用效应子抑制第一层面免疫的病原微生物, 这一过程被称为效应子触发的免疫(Effector-triggered immunity, ETI)。这两个层面的免疫都是基于植物对“自我”及“非我”的识别, 依靠MAPK级联等信号网络, 将识别结果传递到细胞核内, 调控相应基因的表达, 做出适当的免疫应答。本文着重阐述了植物与病原微生物互作过程中不同层面的免疫反应所发生主要事件的分子基础及研究进展。

本文引用格式

程曦,田彩娟,李爱宁,邱金龙 . 植物与病原微生物互作分子基础的研究进展[J]. 遗传, 2012 , 34(2) : 134 -144 . DOI: 10.3724/SP.J.1005.2012.00134

Abstract

Plants have established a complicated immune defense system during co-evolution with pathogens. The innate immune system of plants can be generally divided into two levels. One, named PAMP-triggered immunity (PTI), is based on the recognition of pathogen-associated molecular patterns by pattern-recognition receptors, which confers resistance to most pathogenic microbes. The other begins in cytoplasm and mainly relies on recognition of microbial effectors by plant resistance proteins in direct or indirect ways, which then initiates potent defense responses. This process, termed ef-fector-triggered immunity (ETI), is necessary for defense against pathogens that can secret effectors to suppress the first level of immunity. Activation of these two layers of immunity in plant is based on distinguishing and recognition of “self” and “non-self” signals. Recognition of “non-self” signals can activate signal cascades, such as MAPK cascades, which will then induce defense gene expression and corresponding defense responses. In this review, we focused on underlying mo-lecular mechanisms of plant-pathogen interactions and the latest advances of the PTI and ETI signaling network.

参考文献

[1] Jones JDG, Dangl JL. The plant immune system. Nature, 2006, 444(7117): 323-329.
[2] Boller T, He SY. Innate immunity in plants: an arms race between pattern recognition receptors in plants and effectors in microbial pathogens. Science, 2009, 324(5928): 742-744.
[3] Takken FLW, Tameling WIL. To nibble at plant resistance proteins. Science, 2009, 324(5928): 744-746.
[4] Zipfel C. Pattern-recognition receptors in plant innate immunity. Curr Opin Immunol, 2008, 20(1): 10-16.
[5] Naito K, Taquchi F, Suzuki T, Inagaki Y, Toyoda K, Shiraishi T, Ichinose Y. Amino acid sequence of bacterial microbe-associated molecular pattern flg22 is required for virulence. Mol Plant-Microbe Interact, 2008, 21(9): 1165-1174.
[6] van de Veerdonk FL, Kullberg BJ, van der Meer JW, Gow NA, Netea MG. Host-microbe interactions: innate pattern recognition of fungal pathogens. Curr Opin Micro-biol, 2008, 11(4): 305-312.
[7] Postel S, Kemmerling B. Plant systems for recognition of pathogen-associated molecular patterns. Semin Cell Dev Biol, 2009, 20(9): 1025-1031.
[8] Felix G, Duran JD, Volko S, Boller T. Plants have a sensitive perception system for the most conserved domain of bacterial flagellin. Plant J, 1999, 18(3): 265-276.
[9] Chinchilla D, Bauer Z, Regenass M, Boller T, Felix G. The Arabidopsis receptor kinase FLS2 binds flg22 and determines the specificity of flagellin perception. Plant Cell, 2006, 18(2): 465-476.
[10] Dunning FM, Sun WX, Jansen KL, Helft L, Bent AF. Identification and mutational analysis of Arabidopsis FLS2 leucine-rich repeat domain residues that contribute to flagellin perception. Plant Cell, 2007, 19(10): 3297-3313.
[11] Robatzek S, Bittel P, Chinchilla D, Köchner P, Felix G, Shiu SH, Boller T. Molecular identification and characterization of the tomato flagellin receptor LeFLS2, an orthologue of Arabidopsis FLS2 exhibiting characteristically different perception specificities. Plant Mol Biol, 2007, 64(5): 539-547.
[12] Hann DR, Rathjen JP. Early events in the pathogenicity of Pseudomonas syringae on Nicotiana bentha-miana. Plant J, 2007, 49(4): 607-618.
[13] Takai R, Isogai A, Takayama S, Che FS. Analysis of flag-ellin perception mediated by flg22 receptor OsFLS2 in rice. Mol Plant-Microbe Interact, 2008, 21(12): 1635-1642.
[14] de Torres M, Mansfield JW, Grabov N, Brown IR, Ammouneh H, Tsiamis G, Forsyth A, Robatzek S, Grant M, Boch J. Pseudomonas syringae effector AvrPtoB suppresses basal defence in Arabidopsis. Plant J, 2006, 47(3): 368-382.
[15] Zipfel C, Robatzek S, Navarro L, Oakeley EJ, Jones JD, Felix G, Boller T. Bacterial disease resistance in Arabidopsis through flagellin perception. Nature, 2004, 428(6984): 764-767.
[16] Kunze G, Zipfel C, Robatzek S, Niehaus K, Boller T, Felix G. The N terminus of bacterial elongation factor Tu elicits innate immunity in Arabidopsis plants. Plant Cell, 2004, 16(12): 3496-3507.
[17] Zipfel C, Kunze G, Chinchilla D, Caniard A, Jones JDG, Boller T, Felix G. Perception of the bacterial PAMP EF-Tu by the receptor EFR restricts Agrobacterium-mediated transformation. Cell, 2006, 125(4): 749-760.
[18] Dallo SF, Kannan TR, Blaylock MW, Baseman JB. Elon-gation factor Tu and E1 β subunit of pyruvate dehydro-genase complex act as fibronectin binding proteins in Mycoplasma pneumoniae. Mol Microbiol, 2002, 46(4): 1041-1051.
[19] Granato D, Bergonzelli GE, Pridmore RD, Marvin L, Rouvet M, Corthésy-Theulaz IE. Cell surface-associated elongation factor Tu mediates the attachment of Lactobacillus johnsonii NCC533 (La1) to human intestinal cells and mucins. Infect Immun, 2004, 72(4): 2160-2169.
[20] Lee Sw, Han SW, Sririyanum M, Park CJ, Seo YS, Ronald PC. A
文章导航

/