Department of Agricultural Biology, College of Agriculture and Life Sciences, Chonbuk National University, Jeonju, 561-756, South Korea.
Department of Biotechnology and Animal Science, National Ilan University, Ilan, Taiwan.
Appl Microbiol Biotechnol. 2016 Oct;100(20):8889-900. doi: 10.1007/s00253-016-7734-y. Epub 2016 Jul 28.
The bean bug, Riptortus pedestris, is a major agricultural pest that reduces crop quality and value. Chemical pesticides have contributed to pest management, but resistance to these chemicals has significantly limited their use. Alternative strategies with different modes of action, such as entomopathogenic fungi, are therefore of great interest. Herein, we explored how entomopathogenic fungi can potentially be used to control the bean bug and focused on identifying virulence-related genes. Beauveria bassiana (JEF isolates) were assayed against bean bugs under laboratory conditions. One isolate, JEF-007, showed >80 % virulence by both spray and contact exposure methods. Agrobacterium tumefaciens-mediated transformation (AtMT) of JEF-007 generated 249 random transformants, two of which (B1-06 and C1-49) showed significantly reduced virulence against Tenebrio molitor and R. pedestris immatures. Both species were used for rapid screening of virulence-reduced mutants. The two transformants had different morphologies, conidial production, and thermotolerance than the wild type. To determine the localization of the randomly inserted T-DNA, thermal asymmetric interlaced (TAIL) PCR was conducted and analysis of the two clones found multiple T-DNA insertions (two in B1-06 and three in C1-49). Genes encoding complex I intermediate-associated protein 30 (CIA30) and the autophagy protein (Atg22) were possibly disrupted by the T-DNA insertion and might be involved in the virulence. This work provides a strong platform for future functional genetic studies of bean bug-pathogenic B. bassiana. The genes putatively involved in fungal virulence should be experimentally validated by knockdown in future studies.
豆野螟,又称豆荚野螟,是一种严重的农业害虫,会降低作物的质量和价值。化学农药在害虫治理中发挥了作用,但这些化学物质的抗药性大大限制了它们的使用。因此,具有不同作用模式的替代策略,如昆虫病原真菌,具有很大的吸引力。本文探讨了昆虫病原真菌如何可能用于控制豆野螟,并重点研究了与毒力相关的基因。在实验室条件下,用球孢白僵菌(JEF 分离株)对豆野螟进行了测定。分离株 JEF-007 经喷雾和接触暴露法测定,其毒力均超过 80%。JEF-007 的根癌农杆菌介导的转化(AtMT)产生了 249 个随机转化体,其中两个(B1-06 和 C1-49)对黄粉虫和豆野螟幼虫的毒力显著降低。这两个物种都被用于快速筛选毒力降低的突变体。与野生型相比,这两个转化体具有不同的形态、分生孢子产生和耐热性。为了确定随机插入的 T-DNA 的定位,进行了热不对称交错(TAIL)PCR 分析,对两个克隆的分析发现多个 T-DNA 插入(B1-06 中有两个,C1-49 中有三个)。编码复合体 I 中间相关蛋白 30(CIA30)和自噬蛋白(Atg22)的基因可能被 T-DNA 插入破坏,可能参与了毒力。这项工作为豆野螟致病白僵菌的未来功能遗传研究提供了一个强大的平台。在未来的研究中,应通过敲低实验来验证推测与真菌毒力相关的基因。