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首页> 外文期刊>Applied Microbiology and Biotechnology >Characterization of T-DNA insertion mutants with decreased virulence in the entomopathogenic fungus Beauveria bassiana JEF-007
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Characterization of T-DNA insertion mutants with decreased virulence in the entomopathogenic fungus Beauveria bassiana JEF-007

机译:致病性真菌球孢白僵菌JEF-007中毒力降低的T-DNA插入突变体的表征

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摘要

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.
机译:bug虫(Riptortus pedestris)是一种主要的农业害虫,可降低作物的品质和价值。化学农药有助于病虫害防治,但对这些化学药品的抗性已大大限制了其使用。因此,具有不同作用方式的替代策略,例如昆虫病原真菌,引起了人们的极大兴趣。在这里,我们探讨了昆虫病原性真菌如何可以潜在地用于控制蚕豆,并着重于鉴定与毒力有关的基因。在实验室条件下测定了球孢白僵菌(JEF分离株)对小bug的侵害。通过喷雾和接触暴露方法,一种分离株JEF-007的毒力均大于80%。农杆菌介导的JEF-007转化(AtMT)产生了249个随机转化子,其中两个(B1-06和C1-49)表现出对黄粉虫和pedestris幼虫的毒力明显降低。两种都用于快速筛选降低毒力的突变体。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,对两个克隆的分析发现了多个T-DNA插入(B1-06中两个,C1-49中三个)。编码复合物I中间相关蛋白30(CIA30)和自噬蛋白(Atg22)的基因可能会被T-DNA插入破坏,并可能涉及毒力。这项工作提供了一个强大的平台,为以后的豆虫病致病性球孢白僵菌的功能遗传研究提供了一个平台。推测涉及真菌毒力的基因应在未来的研究中通过敲除实验进行验证。

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