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外源Ca2+对水杨酸诱导番茄抗灰霉病的增效机制

李琳琳1,2,李天来2**,姜国斌1,金华1,邹吉祥1   

  1. (1大连民族大学环境与资源学院, 辽宁大连 116600; 2沈阳农业大学园艺学院, 设施园艺省部共建重点实验室, 沈阳 110866)
  • 出版日期:2015-11-18 发布日期:2015-11-18

Synergistion mechanism of exogenous Ca2+ to SAinduced resistance to Botrytis cinerea in tomato.

LI Lin-lin1,2, LI Tian-lai2, JIANG Guo-bin1, JIN Hua1,  ZOU Ji-xiang1   

  1. (1College of Environment and Resource, Dalian Nationalities University, Dalian 116600, Liaoning, China; 2College of Horticulture, Shenyang Agricultural University, Key Laboratory of Protected Horticulture of Ministry of Education, Shenyang 110866, China)
  • Online:2015-11-18 Published:2015-11-18

摘要:

探讨了外源Ca2+对水杨酸(SA)诱导番茄抗灰霉病的增效机制.以番茄灰霉病敏感型品种‘L402’幼苗为材料,分别进行H2O(对照)、SA、SA+Ca和SA+EGTA(Ca2+螯合剂)处理,期间(1~5 d)分析各处理植株叶片活性氧(ROS)含量,苯丙氨酸解氨酶、几丁质酶和β-1,3-葡聚糖酶活性,以及病程相关蛋白编码基因PR1、PR2PR3表达水平的变化,并调查处理3 d后灰霉病情指数.结果表明: 与对照(病情指数为74.8)相比,SA、SA+Ca和SA+EGTA处理的植株叶片灰霉病的病情指数分别为46.9、38.5和70.3;SA处理明显提高叶片ROS含量以及苯丙氨酸解氨酶、几丁质酶和β-1,3-葡聚糖酶活性,这些参数在SA+Ca处理的植株中被进一步提高,但在SA+EGTA处理的植株中则被降低;SA处理明显提高了PR1、PR2a和PR3b的表达水平,Ca2+进一步加强了这一效果,而EGTA则起抑制作用.SA或SA+Ca处理期间的PR2b和PR3a表达较未处理的对照上调了1~2倍,而PR1、PR2a和PR3b上调了2~5倍.表明Ca2+对SA诱导番茄抗灰霉病具有增效作用,其机理至少与Ca2+和SA协同作用促进ROS形成有关,而ROS作为信号分子增加植株抗病相关酶活性以及PR1、PR2a和PR3b等防卫基因的表达.
 

Abstract: In this study, we investigated the effect of exogenous calcium and salicylic acid (SA) on Botrytis cinerea resistance in tomato seedlings. We treated a tomato strain susceptible to Botrytis cinerea with foliar spraying of water, SA, SA+CaCl2 and SA+EGTA (Ca2+ chelating agent) for one to five days. During the treatment, leaves were collected to analyze the reactive oxygen species (ROS) content, phenylalanine ammonia lyase (PAL) activity, chintase and β-1,3-glucanase levels, and the expression of pathogenesis related protein 1, 2, 3 (PR1, PR2, PR3). Three days after infection, the disease index was
74.8 in control plants, and 46.9, 38.5 and 70.3 in SA, SA+Ca and SA+EGTA 〖JP〗treated plants, respectively. SA treatment significantly increased ROS leaf accumulation, and activities of PAL, chintase and β-1,3-glucanase. These values were further enhanced in SA+Ca treated plants, but decreased in SA+EGTA treated plants. Application of SA significantly increased the expression levels of PR1, PR2a and PR3b, which were further elevated by the combination treatment with Ca2+. These effects were counteracted by the combination treatment of SA and EGTA. The transcription levels of PR2b and PR3a were upregulated by 1-2 folds, and PR1, 2a and 3b by 2-5 folds in SA and SA+Catreated plants relative to control. These data suggested that application of Ca2+ could synergistically increase SAinduced resistance to B. cinerea. The resistance was associated with ROS accumulation, therefore the increase in resistance might be through ROS ability to increase the activity of defenserelated enzymes and expression levels of PR1, PR2a and PR3b.