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昆虫病原真菌球孢白僵菌形成附着胞和穿透昆虫表皮所需的丝裂原活化蛋白激酶。

Requirement of a mitogen-activated protein kinase for appressorium formation and penetration of insect cuticle by the entomopathogenic fungus Beauveria bassiana.

机构信息

Key Laboratory of Biotechnology and Crop Quality Improvement of the Ministry of Agriculture of China, Biotechnology Research Center, Southwest University, Chongqing 400716, People's Republic of China.

出版信息

Appl Environ Microbiol. 2010 Apr;76(7):2262-70. doi: 10.1128/AEM.02246-09. Epub 2010 Feb 5.

DOI:10.1128/AEM.02246-09
PMID:20139313
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2849248/
Abstract

Beauveria bassiana is an important insect-pathogenic fungus that invades insects by direct penetration of the host cuticle. To delineate the molecular mechanisms involved in fungal infection, a mitogen-activated protein kinase (MAPK) gene, Bbmpk1, which encodes a YERK1 family MAPK was isolated and characterized. Targeted gene disruption of Bbmpk1 resulted in a complete loss of virulence when applied topically to host insects but did not affect growth of the fungus when conidia were injected directly into the hemocoel. Hyphae of the mutant strain growing in the insect hemocoel were unable to penetrate the cuticle growing outwards and consequently failed to sporulate on the cadaver surface. These data suggest that BbMPK1 is essential for penetration of the insect cuticle both from the outside and from the inside-out in order to escape and disperse from the host. Inactivation of BbMPK1 also caused a significant decrease in fungal adhesion to insect cuticles and eliminated their ability to form appressoria. In order to identify downstream genes regulated by BbMPK1, a suppressive subtractive hybridization (SSH) library was generated comparing mutant and wild-type transcripts isolated during appressorium formation. Thirty-one genes screened from the SSH library were determined to be expressed in the wild-type strain but either significantly reduced or not expressed in the mutant. Ten genes showed high or medium similarity to known protein encoding genes, including proteins involved in cell surface hydrophobicity, lipid metabolism, microtubule dynamics, mitochondrial electron transport, chromatin remodeling, transcription, rRNA processing, small nucleolar RNA accumulation, oxidation of aldehydes, translation, and likely other cellular processes.

摘要

球孢白僵菌是一种重要的昆虫病原真菌,通过直接穿透宿主表皮来感染昆虫。为了阐明真菌感染涉及的分子机制,分离并鉴定了一个编码 YERK1 家族 MAPK 的丝裂原活化蛋白激酶(MAPK)基因 Bbmpk1。靶向基因敲除 Bbmpk1 导致该基因在对宿主昆虫进行局部应用时完全丧失毒力,但当将分生孢子直接注射到血腔中时,并不影响真菌的生长。在昆虫血腔中生长的突变菌株的菌丝无法穿透向外生长的表皮,因此无法在尸体表面产孢。这些数据表明,BbMPK1 对于从外部和内部穿透昆虫表皮以逃脱并从宿主中扩散是必不可少的。BbMPK1 的失活也导致真菌对昆虫表皮的粘附显著减少,并消除了其形成附着胞的能力。为了鉴定由 BbMPK1 调控的下游基因,通过比较在附着胞形成过程中分离的突变体和野生型转录本,生成了抑制性消减杂交(SSH)文库。从 SSH 文库中筛选出的 31 个基因在野生型菌株中表达,但在突变体中表达显著降低或不表达。其中 10 个基因与已知的编码蛋白基因具有高度或中等相似性,包括参与细胞表面疏水性、脂质代谢、微管动力学、线粒体电子传递、染色质重塑、转录、rRNA 加工、小核仁 RNA 积累、醛氧化、翻译以及可能的其他细胞过程的蛋白质。

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Biosynthesis of the cyclooligomer depsipeptide bassianolide, an insecticidal virulence factor of Beauveria bassiana.球孢白僵菌的杀虫毒力因子环寡聚缩肽白僵菌素的生物合成
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