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苜蓿与兼容和不兼容细菌(野油菜黄单胞菌苜蓿致病变种和丁香假单胞菌豌豆致病变种)相互作用的病理学和分子特征

Pathological and molecular characterizations of alfalfa interactions with compatible and incompatible bacteria, Xanthomonas campestris pv. alfalfae and Pseudomonas syringae pv. pisi.

作者信息

Esnault R, Buffard D, Breda C, Sallaud C, el Turk J, Kondorosi A

机构信息

Institut des Sciences Végétales, C.N.R.S., Gif-sur-Yvette, France.

出版信息

Mol Plant Microbe Interact. 1993 Sep-Oct;6(5):655-64. doi: 10.1094/mpmi-6-655.

Abstract

We report on the interactions of alfalfa with Xanthomonas campestris pv. alfalfae and Pseudomonas syringae pv. pisi. A hypersensitive response was observed when leaves were infiltrated with P. s. pv. pisi, which remained strictly limited to the injected zone. The compatible interaction with X. c. pv. alfalfae was characterized by water-soaking symptoms and the spreading of the bacterium into the leaf blade. Analyses of transcript accumulation were conducted with cDNAs encoding enzymes involved in phytoalexin synthesis: chalcone synthase (CHS), chalcone isomerase (CHI), and isoflavone reductase (IFR). In incompatible interactions the maximum accumulation of the CHS, CHI, and IFR transcripts was observed 6 hr postinfection. In the compatible interaction, the induction of these transcripts was delayed until 25-30 hr postinfection, and the level of their accumulation was considerably lower. Extending this molecular analysis to the root system showed that the reaction of roots during an incompatible interaction was quite comparable to that of leaves. To complete these analyses, expression of genes encoding pathogenesis-related (PR) proteins in leaves was also analyzed by polymerase chain reaction. High-level accumulation of a 0.8-kb transcript encoding a PR protein was observed 6 to 30 hr postinfection in the incompatible interaction.

摘要

我们报告了苜蓿与苜蓿黄单胞菌苜蓿致病变种(Xanthomonas campestris pv. alfalfae)以及豌豆假单胞菌豌豆致病变种(Pseudomonas syringae pv. pisi)之间的相互作用。当用豌豆假单胞菌豌豆致病变种浸润叶片时,观察到了过敏反应,该反应严格局限于注射区域。与苜蓿黄单胞菌苜蓿致病变种的亲和性相互作用表现为水渍状症状以及细菌向叶片扩散。利用编码参与植保素合成的酶的cDNA进行了转录本积累分析:查尔酮合酶(CHS)、查尔酮异构酶(CHI)和异黄酮还原酶(IFR)。在不亲和相互作用中,感染后6小时观察到CHS、CHI和IFR转录本的最大积累量。在亲和性相互作用中,这些转录本的诱导延迟至感染后25 - 30小时,且其积累水平显著较低。将这种分子分析扩展到根系表明,在不亲和相互作用期间根系的反应与叶片相当。为完成这些分析,还通过聚合酶链反应分析了叶片中编码病程相关(PR)蛋白的基因的表达。在不亲和相互作用中,感染后6至30小时观察到编码一种PR蛋白的0.8 kb转录本的高水平积累。

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