Du Nanshan, Shi Lu, Yuan Yinghui, Li Bin, Shu Sheng, Sun Jin, Guo Shirong
Key Laboratory of Southern Vegetable Crop Genetic Improvement in Ministry of Agriculture, College of Horticulture, Nanjing Agricultural University Nanjing, China.
Department of Horticulture, Shanxi Agricultural University Taigu, China.
Front Plant Sci. 2016 Dec 14;7:1859. doi: 10.3389/fpls.2016.01859. eCollection 2016.
Plant-growth-promoting rhizobacteria (PGPR) can both improve plant growth and enhance plant resistance against a variety of environmental stresses. To investigate the mechanisms that PGPR use to protect plants under pathogenic attack, transmission electron microscopy analysis and a proteomic approach were designed to test the effects of the new potential PGPR strain NSY50 on cucumber seedling roots after they were inoculated with the destructive phytopathogen f. sp. (FOC). NSY50 could apparently mitigate the injury caused by the FOC infection and maintain the stability of cell structures. The two-dimensional electrophoresis (2-DE) approach in conjunction with MALDI-TOF/TOF analysis revealed a total of 56 proteins that were differentially expressed in response to NSY50 and/or FOC. The application of NSY50 up-regulated most of the identified proteins that were involved in carbohydrate metabolism and amino acid metabolism under normal conditions, which implied that both energy generation and the production of amino acids were enhanced, thereby ensuring an adequate supply of amino acids for the synthesis of new proteins in cucumber seedlings to promote plant growth. Inoculation with FOC inhibited most of the proteins related to carbohydrate and energy metabolism and to protein metabolism. The combined inoculation treatment (NSY50+FOC) accumulated abundant proteins involved in defense mechanisms against oxidation and detoxification as well as carbohydrate metabolism, which might play important roles in preventing pathogens from attacking. Meanwhile, western blotting was used to analyze the accumulation of enolase (ENO) and S-adenosylmethionine synthase (SAMs). NSY50 further increased the expression of ENO and SAMs under FOC stress. In addition, NSY50 adjusted the transcription levels of genes related to those proteins. Taken together, these results suggest that NSY50 may promote plant growth and alleviate FOC-induced damage by improving the metabolism and activation of defense-related proteins in cucumber roots.
植物促生根际细菌(PGPR)既能促进植物生长,又能增强植物对多种环境胁迫的抗性。为了探究PGPR在病原菌攻击下保护植物的机制,设计了透射电子显微镜分析和蛋白质组学方法,以测试新型潜在PGPR菌株NSY50对接种毁灭性植物病原菌尖孢镰刀菌古巴专化型(FOC)后的黄瓜幼苗根系的影响。NSY50能够明显减轻FOC感染造成的损伤,并维持细胞结构的稳定性。二维电泳(2-DE)方法结合基质辅助激光解吸电离飞行时间串联质谱(MALDI-TOF/TOF)分析,共鉴定出56种因NSY50和/或FOC处理而差异表达的蛋白质。在正常条件下,NSY50的施用上调了大多数已鉴定的参与碳水化合物代谢和氨基酸代谢的蛋白质,这意味着能量生成和氨基酸的产生均得到增强,从而确保为黄瓜幼苗新蛋白质的合成提供充足的氨基酸供应,以促进植物生长。接种FOC抑制了大多数与碳水化合物、能量代谢以及蛋白质代谢相关的蛋白质。联合接种处理(NSY50+FOC)积累了大量参与抗氧化和解毒防御机制以及碳水化合物代谢的蛋白质,这可能在防止病原体攻击中发挥重要作用。同时,采用蛋白质免疫印迹法分析烯醇化酶(ENO)和S-腺苷甲硫氨酸合成酶(SAMs)的积累情况。在FOC胁迫下,NSY50进一步增加了ENO和SAMs的表达。此外,NSY50还调节了与这些蛋白质相关基因的转录水平。综上所述,这些结果表明NSY50可能通过改善黄瓜根系中防御相关蛋白质的代谢和激活来促进植物生长并减轻FOC诱导的损伤。