Nazir Talha, Hanan Abdul, Basit Abdul, Majeed Muhammad Zeeshan, Anwar Tauqir, Nawaz Iqra, Qiu Dewen
State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing 100081, China.
Department of Entomology, College of Agriculture, University of Sargodha, Sargodha 40100, Pakistan.
Pathogens. 2020 Feb 11;9(2):111. doi: 10.3390/pathogens9020111.
This study reports the characterization of protein elicitor PeBb1 derived from entomopathogenic fungus ARSEF-2860 strain and its putative role in induced systemic resistance in ssp. against green peach aphid . The sequence of purified elicitor protein was matched with the genomic sequence of a hypothetical protein BBA_10269 from ARSEF-2860 (GenBank Accession No. XP_008603588.1). The protein-encoding gene contained 534 bp cDNA encoding a polypeptide of 177 amino acids with a molecular mass of 19 kDa. The recombinant elicitor protein was expressed in using pET-28a (+) expression vector and induced necrosis in the leaves of tobacco. The effects of elicitor protein on aphid was determined by applying three different concentrations of PeBb1 (i.e., 26, 35, 53 μM) on plants at 4-leaf stage and the treated plants were exposed to newly emerged (0-6 h old) apterous adult aphids. Bioassay results showed significant ( < 0.05) sub-lethal effects of the exogenous application of PeBb1 elicitor on . Moreover, the RT-qPCR gene expression analyses showed a significant up-regulation of most of the key genes linked to ethylene (ET)- and jasmonic acid (JA)-associated plant defense pathways in elicitor-treated plants. These results not only recommend the putative utilization of PeBb1 elicitor protein in future biological pest control strategies against phloem-feeding insect pests such as , but also help in better comprehension of the mechanisms through which beneficial fungi trigger the induced plant resistance.
本研究报道了源自昆虫病原真菌ARSEF - 2860菌株的蛋白激发子PeBb1的特性及其在诱导马铃薯对桃蚜的系统抗性中的假定作用。纯化的激发子蛋白序列与ARSEF - 2860的假定蛋白BBA_10269(GenBank登录号:XP_008603588.1)的基因组序列相匹配。该蛋白质编码基因包含534 bp的cDNA,编码一个由177个氨基酸组成、分子量为19 kDa的多肽。重组激发子蛋白在大肠杆菌中使用pET - 28a(+)表达载体进行表达,并在烟草叶片中诱导坏死。通过在四叶期的马铃薯植株上施用三种不同浓度的PeBb1(即26、35、53 μM)来测定激发子蛋白对蚜虫的影响,处理后的植株暴露于新出现的(0 - 6小时龄)无翅成年蚜虫中。生物测定结果表明,外源施用PeBb1激发子对马铃薯有显著(P < 0.05)的亚致死效应。此外,RT - qPCR基因表达分析表明,在激发子处理的植株中,与乙烯(ET)和茉莉酸(JA)相关的植物防御途径的大多数关键基因显著上调。这些结果不仅推荐了在未来针对韧皮部取食害虫如桃蚜的生物防治策略中假定利用PeBb1激发子蛋白,而且有助于更好地理解有益真菌触发诱导植物抗性的机制。