Marco Maria L, Legac Jennifer, Lindow Steven E
Department of Plant and Microbial Biology, University of California, Berkeley, CA 94720, USA.
Environ Microbiol. 2005 Sep;7(9):1379-91. doi: 10.1111/j.1462-2920.2005.00825.x.
The foliar pathogen and ice nucleator, Pseudomonas syringae pv. syringae B728a, demonstrates a high level of epiphytic fitness on plants. Using a promoter-trapping strategy termed habitat-inducible rescue of survival (HIRS), we identified genes of this organism that are induced during colonization of healthy bean leaf surfaces. These plant-inducible genes (pigs) encode diverse cellular functions including virulence, transcription regulation, transport, nutrient acquisition and other known and unknown loci, some of which may result in antisense transcripts to annotated P. syringae genes. Prominent among the pigs was ssuE, a gene in the sulfate-starvation regulon, indicating that sulfate is not abundant on leaf surfaces. inaZ reporter gene fusion assays of the plant-inducible loci revealed up to 300-fold higher levels of pig transcriptional activity on plant leaves compared with minimal medium. However, the maximum levels of pig transcriptional activity were typically too weak to be measured using a gfp reporter gene. One exception was orf6 in the hrp/hrc pathogenicity island which was highly induced in epiphytic P. syringae cells. Four pigs were disrupted by insertional mutagenesis. While growth of the ssuE mutant was impaired under certain conditions in laboratory medium, the epiphytic and virulence properties of the mutants on bean plants were identical to wild-type P. syringae. Our results demonstrate the utility of HIRS to identify genes expressed on leaves and provide new insight into the leaf surface environment.
叶部病原菌及冰核细菌丁香假单胞菌丁香致病变种B728a在植物上表现出高度的附生适应性。利用一种称为生存生境诱导拯救(HIRS)的启动子捕获策略,我们鉴定出了该生物体在健康菜豆叶表面定殖过程中被诱导表达的基因。这些植物诱导基因(pigs)编码多种细胞功能,包括毒力、转录调控、转运、养分获取以及其他已知和未知的基因座,其中一些可能产生与注释的丁香假单胞菌基因对应的反义转录本。在这些植物诱导基因中,突出的是硫酸饥饿调节子中的ssuE基因,这表明叶表面的硫酸盐并不丰富。对植物诱导基因座进行的inaZ报告基因融合分析显示,与基本培养基相比,植物叶片上植物诱导基因的转录活性水平高出300倍。然而,植物诱导基因的转录活性最高水平通常较弱,无法使用绿色荧光蛋白(gfp)报告基因进行检测。一个例外是hrp/hrc致病岛中的orf6基因,其在附生的丁香假单胞菌细胞中高度诱导表达。通过插入诱变破坏了四个植物诱导基因。虽然ssuE突变体在实验室培养基的某些条件下生长受到损害,但其在菜豆植物上的附生和毒力特性与野生型丁香假单胞菌相同。我们的结果证明了HIRS在鉴定叶片上表达的基因方面的实用性,并为叶表面环境提供了新的见解。