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利用嵌合低毒病毒微调致病真菌与其植物宿主之间的相互作用。

Using chimeric hypoviruses to fine-tune the interaction between a pathogenic fungus and its plant host.

作者信息

Chen B, Geletka L M, Nuss D L

机构信息

Center for Agricultural Biotechnology, University of Maryland Biotechnology Institute, College Park, Maryland 20742-4450, USA.

出版信息

J Virol. 2000 Aug;74(16):7562-7. doi: 10.1128/jvi.74.16.7562-7567.2000.

Abstract

Infectious cDNA clones of mild (CHV1-Euro7) and severe (CHV1-EP713) hypovirus strains responsible for virulence attenuation (hypovirulence) of the chestnut blight fungus Cryphonectria parasitica were used to construct viable chimeric viruses. Differences in virus-mediated alterations of fungal colony morphology, growth rate, and canker morphology were mapped to a region of open reading frame B extending from nucleotides 2,363 to 9, 904. By swapping domains within this region, it was possible to generate chimeric hypovirus-infected C. parasitica isolates that exhibited a spectrum of defined colony and canker morphologies. Several severe strain traits were observed to be dominant. It was also possible to uncouple the severe strain traits of small canker size and suppression of asexual sporulation. For example, fungal isolates infected with a chimera containing nucleotides 2363 through 5310 from CHV1-Euro7 in a CHV1-713 background formed small cankers that were similar in size to that caused by CHV1-EP713-infected isolates but with the capacity for producing asexual spores at levels approaching that observed for fungal isolates infected with the mild strain. These results demonstrate that hypoviruses can be engineered to fine-tune the interaction between a pathogenic fungus and its plant host. The identification of specific hypovirus domains that differentially contribute to canker morphology and sporulation levels also provides considerable utility for continuing efforts to enhance biological control potential by balancing hypovirulence and ecological fitness.

摘要

负责栗疫病菌致病力减弱(低毒力)的温和型(CHV1-Euro7)和严重型(CHV1-EP713)低毒病毒株的感染性cDNA克隆被用于构建有活力的嵌合病毒。病毒介导的真菌菌落形态、生长速率和溃疡形态变化的差异被定位到开放阅读框B从核苷酸2363到9904的区域。通过在该区域内交换结构域,有可能产生表现出一系列明确的菌落和溃疡形态的嵌合低毒病毒感染的寄生隐孢壳菌分离株。观察到几个严重型菌株的性状是显性的。也有可能将溃疡面积小和抑制无性孢子形成的严重型菌株性状分开。例如,在CHV1-713背景下,感染含有来自CHV1-Euro7的核苷酸2363至5310的嵌合体的真菌分离株形成的小溃疡与CHV1-EP713感染的分离株引起的溃疡大小相似,但产生无性孢子的能力接近温和型菌株感染的真菌分离株所观察到的水平。这些结果表明,可以对低毒病毒进行改造,以微调致病真菌与其植物宿主之间的相互作用。鉴定对溃疡形态和孢子形成水平有不同贡献的特定低毒病毒结构域,对于通过平衡低毒力和生态适应性来持续提高生物防治潜力的努力也具有相当大的实用价值。

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