Isolation and identification of a virulent Ralstonia solanacearum by fliC gene amplification and induction of chitinase by 2-amino butyric acid for control of bacterial wilt in tomato plants

A. Saha, H. Mandal, D. Saha
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Abstract

Ralstonia solanacearum is a devastating, soil borne bacterial pathogen of tomato. The pathogen is nonmotile in planta but highly motile in culture. On the basis of physiological and biochemical characteristics 26 isolates have been purified and identified as Ralstonia solanacearum. The flic gene is responsible for the movement of bacteria. Ralstonia specific fliC gene amplification is the indication of virulence of the pathogen. In the present study one R. solanacearum isolate has been identified by PCR amplification of the fliC gene using fliC gene specific primer. Following isolation and identification of the virulent isolate, fresh tomato plants were induced by application of 2- amino butyric acid (ABA). The defense enzyme, chitinase was estimated in treated plants. Treated inoculated plants did not show any visible symptoms of wilt even after 14 days of inoculation. Significantly it was observed that chitinase was increased in the 2-ABA-treated plants and also in the treated-inoculated plants. The increased chitinase activity in the treated plants showed that 2-ABA has the resistance inducing capacity in tomato plants against Ralstonia solanacearum.
利用fliC基因扩增和2-氨基丁酸诱导几丁质酶对番茄青枯病毒力的分离鉴定
番茄青枯病是一种具有破坏性的土壤致病菌。病原菌在植物中不活动,但在培养物中活动能力强。根据生理生化特征,对26株病原菌进行了纯化鉴定。fllic基因负责细菌的运动。Ralstonia特异性fliC基因扩增是病原体毒力的指示。本研究用fliC基因特异性引物对一株茄红真菌进行了fliC基因的PCR扩增。在对毒力分离物进行分离鉴定后,用2-氨基丁酸(ABA)诱导番茄植株生长。对处理植株的防御酶几丁质酶进行了测定。接种14天后,接种植株也未出现明显的萎蔫症状。2- aba处理的植株和接种的植株几丁质酶均显著升高。处理植株几丁质酶活性升高,表明2-ABA具有诱导番茄抗青枯病的能力。
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