Gene expression analysis in cucumber leaves primed by root colonization with Pseudomonas chlororaphis O6 upon challenge-inoculation with Corynespora cassiicola

被引:43
作者
Kim, MS
Kim, YC
Cho, BH [1 ]
机构
[1] Chonnam Natl Univ, Div Appl Plant Sci, Coll Agr & Life Sci, Inst Agr Sci & Technol, Kwangju 500757, South Korea
[2] Chonnam Natl Univ, Agr Plant Stress Res Ctr, Kwangju 500757, South Korea
关键词
Corynespora cassiicola; induced systemic resistance; priming phenomenon; Pseudomonas chlororaphis; root colonization; target leaf spot;
D O I
10.1055/s-2004-817803
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Root colonization by Pseudomonas chlororaphis O6, a non-pathogenic rhizobacterium, induced systemic resistance in cucumber against target leaf spot caused by Corynespora cassicola. A cDNA library was constructed using mRNA extracted from cucumber leaves 12 h after inoculation with C. cassiicola, using plants colonized by O6. To identify genes involved in O6-mediated induced systemic resistance (ISR), we employed a subtractive hybridization method using mRNAs extracted from pathogen-challenged cucumber leaves of plants lacking colonization. Differential screening of the cDNA library led to the isolation of six distinct genes encoding a GTP binding protein, a 60S ribosomal protein, a hypersensitive-induced reaction protein, a ubiquitin extension protein, a pyridine nucleotide-disulfide oxidoreductase, and a signal recognition particle receptor. Expression of these genes was not induced by O6 colonization alone. Rather, transcript accumulation of these genes increased significantly faster and stronger in the O6 colonized than in non-colonized plants after challenge infection. Therefore, O6-mediated ISR may be associated with an enhanced capacity for the rapid and effective activation of cellular defence responses after challenge inoculation.
引用
收藏
页码:105 / 108
页数:4
相关论文
共 19 条
[1]   Induction of defense-related ultrastructural modifications in pea root tissues inoculated with endophytic bacteria [J].
Benhamou, N ;
Kloepper, JW ;
QuadtHallman, A ;
Tuzun, S .
PLANT PHYSIOLOGY, 1996, 112 (03) :919-929
[2]   Priming in plant-pathogen interactions [J].
Conrath, U ;
Pieterse, CMJ ;
Mauch-Mani, B .
TRENDS IN PLANT SCIENCE, 2002, 7 (05) :210-216
[3]  
Dangl JL, 1996, PLANT CELL, V8, P1793, DOI 10.1105/tpc.8.10.1793
[4]   ISOLATION AND CHARACTERIZATION OF TOMATO CDNA AND GENOMIC CLONES ENCODING THE UBIQUITIN GENE UBI3 [J].
HOFFMAN, NE ;
KO, K ;
MILKOWSKI, D ;
PICHERSKY, E .
PLANT MOLECULAR BIOLOGY, 1991, 17 (06) :1189-1201
[5]  
Huang HT, 2000, CANCER RES, V60, P6868
[6]   Up-regulation of PDCD4 in senescent human diploid fibroblasts [J].
Kang, MJ ;
Ahn, HS ;
Lee, JY ;
Matsuhashi, S ;
Park, WY .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 293 (01) :617-621
[7]   Identification and characterization of transcription factor IIIA and ribosomal protein L5 from Arabidopsis thaliana [J].
Mathieu, O ;
Yukawa, Y ;
Prieto, JL ;
Vaillant, I ;
Sugiura, M ;
Tourmente, S .
NUCLEIC ACIDS RESEARCH, 2003, 31 (09) :2424-2433
[8]   Prohibitins, stomatins, and plant disease response genes compose a protein superfamily that controls cell proliferation, ion channel regulation, and death [J].
Nadimpalli, R ;
Yalpani, N ;
Johal, GS ;
Simmons, CR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (38) :29579-29586
[9]   Activation of PR-1a promoter by rhizobacteria that induce systemic resistance in tobacco against Pseudomonas syringae pv. tabaci [J].
Park, KS ;
Kloepper, JW .
BIOLOGICAL CONTROL, 2000, 18 (01) :2-9
[10]   A novel signaling pathway controlling induced systemic resistance in Arabidopsis [J].
Pieterse, CMJ ;
van Wees, SCM ;
van Pelt, JA ;
Knoester, M ;
Laan, R ;
Gerrits, N ;
Weisbeek, PJ ;
van Loon, LC .
PLANT CELL, 1998, 10 (09) :1571-1580