首页> 外文期刊>Biological Control: Theory and Application in Pest Management >A phcA(-) marker-free mutant of Ralstonia solanacearum as potential biocontrol agent of tomato bacterial wilt
【24h】

A phcA(-) marker-free mutant of Ralstonia solanacearum as potential biocontrol agent of tomato bacterial wilt

机译:青枯雷尔氏菌无phcA(-)标记突变体作为番茄青枯病的潜在生物防治剂

获取原文
获取原文并翻译 | 示例
           

摘要

A phcA mutant of Ralstonia solanacearum strain ZJ3721 was created in a marker-free method. Expression of virulence-associated genes such as xpsR, egl, tek and epsE was significantly suppressed in the phcA mutant. The ability of the mutant to control tomato bacterial wilt was evaluated by potting experiment. Results showed that application of mutant with wild type (WT) at the same time only delayed the development of wilt for about one day and the population of WT in tomato rhizosphere soil was nearly 70-fold higher than that of the mutant, resulting in a 90% disease incidence at last, as high as that of control. If the phcA mutant was applied three days earlier than WT pathogen, tomato wilt disease incidence was only 6%, 80% lower than that of control and population of WT was about 0.5-fold as much as that of mutant. Under hydroponic conditions, phcA mutant significantly triggered the expressions of genes in salicylic acid pathway but inhibited the expressions of genes in jasmonic acid (JA) and ethylene (ET) pathways. The expressions of PR-1a and GluA genes (salicylic acid pathway) in phcA mutant were 66-fold and 7.5-fold higher than in WT pathogen after three days of inoculation. (C) 2014 Elsevier Inc. All rights reserved.
机译:无标记法创建青枯雷尔氏菌菌株ZJ3721的phcA突变体。在phcA突变体中,与毒力相关的基因(例如xpsR,egl,tek和epsE)的表达被显着抑制。通过盆栽实验评估了该突变体控制番茄青枯病的能力。结果表明,同时施用野生型(WT)突变体仅将枯萎发育推迟了约一天,番茄根际土壤中的WT种群比突变体高了近70倍,导致最终该病的发病率达90%,与对照组一样高。如果将phcA突变体比野生型病原体提前三天使用,那么番茄枯萎病的发病率仅比对照组低6%,比对照组低80%,而野生型群体的数量约为突变体的0.5倍。在水培条件下,phcA突变体显着触发了水杨酸途径中基因的表达,但抑制了茉莉酸(JA)和乙烯(ET)途径中的基因的表达。接种三天后,phcA突变体中PR-1a和GluA基因(水杨酸途径)的表达分别比WT病原体高66倍和7.5倍。 (C)2014 Elsevier Inc.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号