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在生物膜形成过程中和应对不同环境挑战时,铜绿假单胞菌中 hrpM/opgH 基因的转录研究。

Transcriptional studies of the hrpM/opgH gene in Pseudomonas syringae during biofilm formation and in response to different environmental challenges.

机构信息

127 Noble Research Center, Department of Entomology and Plant Pathology, Oklahoma State University, Stillwater, OK 74078, USA.

出版信息

Environ Microbiol. 2010 Jun;12(6):1452-67. doi: 10.1111/j.1462-2920.2010.02160.x. Epub 2010 Feb 2.

Abstract

Pseudomonas syringae pv. syringae strain FF5 is a phytopathogen that causes a rapid dieback on ornamental pear trees. In the present study, the transcriptional expression of hrpM/opgH, algD, hrpR and rpoD was evaluated in P. syringae FF5 and FF5.M2 (hrpM/opgH mutant). The temporal expression of these genes was evaluated during biofilm formation, the hypersensitive reaction (HR) on tobacco plants, and when the bacteria were subjected to different environmental stresses. The results indicate that mutations in hrpM negatively impair several traits including biofilm formation, the ability to cause disease in host plants and the HR in non-host plants, and the expression of hrpR, a regulatory gene modulating the latter two traits. Furthermore, FF5.M2 was decreased in swarming motility and unable to respond to different environmental challenges. Interestingly, FF5.M2 showed an exponential increase in the expression of algD, which is the first gene to be transcribed during the biosynthesis of the alginate, a virulence factor in P. syringae. The expression of both hrpM and algD were required for biofilm formation, and hrpM was expressed earlier than algD during biofilm development. These findings indicate that hrpM expression is required for several traits in P. syringae and plays an important role in how this bacterium responds to environmental challenges.

摘要

丁香假单胞菌 pv. 丁香致病变种 FF5 是一种植物病原体,可导致观赏梨树迅速枯萎。在本研究中,评估了 hrpM/opgH、algD、hrpR 和 rpoD 在丁香假单胞菌 FF5 和 FF5.M2(hrpM/opgH 突变体)中的转录表达。在生物膜形成、烟草植物上的过敏反应(HR)以及细菌受到不同环境压力时,评估了这些基因的时间表达。结果表明,hrpM 突变负向削弱了包括生物膜形成、在宿主植物中致病能力和非宿主植物中的 HR 在内的几种性状,以及调节后两种性状的调节基因 hrpR 的表达。此外,FF5.M2 的群集运动能力降低,无法应对不同的环境挑战。有趣的是,FF5.M2 中 algD 的表达呈指数增长,algD 是在 alginate 生物合成中第一个被转录的基因,alginate 是丁香假单胞菌的一种毒力因子。algD 的表达对于生物膜形成是必需的,并且在生物膜发育过程中 hrpM 的表达早于 algD。这些发现表明,hrpM 的表达是丁香假单胞菌中几种性状所必需的,并且在该细菌如何响应环境挑战方面发挥着重要作用。

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