Chen Z, Kloek A P, Boch J, Katagiri F, Kunkel B N
Department of Biology, Washington University, St. Louis, MO 63130, USA.
Mol Plant Microbe Interact. 2000 Dec;13(12):1312-21. doi: 10.1094/MPMI.2000.13.12.1312.
Several bacterial avr genes have been shown to contribute to virulence on susceptible plants lacking the corresponding resistance (R) gene. The mechanisms by which avr genes promote parasitism and disease, however, are not well understood. We investigated the role of the Pseudomonas syringae pv. tomato avrRpt2 gene in pathogenesis by studying the interaction of P. syringae pv. tomato strain PstDC3000 expressing avrRpt2 with several Arabidopsis thaliana lines lacking the corresponding R gene, RPS2. We found that PstDC3000 expressing avrRpt2 grew to significantly higher levels and often resulted in the formation of more severe disease symptoms in ecotype No-0 plants carrying a mutant RPS2 allele, as well as in two Col-0 mutant lines, cpr5 rps2 and coil rps2, that exhibit enhanced resistance. We also generated transgenic A. thaliana lines expressing avrRpt2 and demonstrated, by using several different assays, that expression of avrRpt2 within the plant also promotes virulence of PstDC3000. Thus, AvrRpt2 appears to promote pathogen virulence from within the plant cell.
一些细菌的无毒基因(avr基因)已被证明,在缺乏相应抗性(R)基因的感病植物上,这些基因有助于病原菌的致病力。然而,avr基因促进寄生和致病的机制尚未完全清楚。我们通过研究表达avrRpt2的丁香假单胞菌番茄致病变种(Pseudomonas syringae pv. tomato)与几个缺乏相应R基因RPS2的拟南芥品系之间的相互作用,来探究avrRpt2基因在致病过程中的作用。我们发现,表达avrRpt2的PstDC3000在携带突变RPS2等位基因的生态型No-0植物以及两个表现出增强抗性的Col-0突变系cpr5 rps2和coil rps2中,生长到显著更高的水平,并且常常导致更严重的病害症状。我们还构建了表达avrRpt2的转基因拟南芥品系,并通过几种不同的检测方法证明,avrRpt2在植物体内的表达也促进了PstDC3000的致病力。因此,AvrRpt2似乎从植物细胞内部促进了病原菌的致病力。