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通过多位点vic基因的系统性破坏构建栗疫病菌的工程化超级真菌病毒供体菌株。

Engineering super mycovirus donor strains of chestnut blight fungus by systematic disruption of multilocus vic genes.

作者信息

Zhang Dong-Xiu, Nuss Donald L

机构信息

Institute for Bioscience and Biotechnology Research and Department of Cell Biology and Molecular Genetics, University of Maryland, Rockville, MD 20850.

Institute for Bioscience and Biotechnology Research and Department of Cell Biology and Molecular Genetics, University of Maryland, Rockville, MD 20850

出版信息

Proc Natl Acad Sci U S A. 2016 Feb 23;113(8):2062-7. doi: 10.1073/pnas.1522219113. Epub 2016 Feb 8.

Abstract

Transmission of mycoviruses that attenuate virulence (hypovirulence) of pathogenic fungi is restricted by allorecognition systems operating in their fungal hosts. We report the use of systematic molecular gene disruption and classical genetics for engineering fungal hosts with superior virus transmission capabilities. Four of five diallelic virus-restricting allorecognition [vegetative incompatibility (vic)] loci were disrupted in the chestnut blight fungus Cryphonectria parasitica using an adapted Cre-loxP recombination system that allowed excision and recycling of selectable marker genes (SMGs). SMG-free, quadruple vic mutant strains representing both allelic backgrounds of the remaining vic locus were then produced through mating. In combination, these super donor strains were able to transmit hypoviruses to strains that were heteroallelic at one or all of the virus-restricting vic loci. These results demonstrate the feasibility of modulating allorecognition to engineer pathogenic fungi for more efficient transmission of virulence-attenuating mycoviruses and enhanced biological control potential.

摘要

降低致病真菌毒力(低毒力)的真菌病毒的传播受到其真菌宿主中运行的异体识别系统的限制。我们报告了使用系统分子基因破坏和经典遗传学来改造具有卓越病毒传播能力的真菌宿主。利用一种经过改良的Cre-loxP重组系统,在栗疫病菌Cryphonectria parasitica中破坏了五个双等位基因病毒限制异体识别[营养体不亲和性(vic)]位点中的四个,该系统允许切除和循环利用选择标记基因(SMG)。然后通过交配产生了代表剩余vic位点两个等位基因背景的无SMG四重vic突变体菌株。这些超级供体菌株组合起来,能够将低毒病毒传播给在一个或所有病毒限制vic位点上具有异等位基因的菌株。这些结果证明了调节异体识别以改造致病真菌从而更有效地传播毒力减弱的真菌病毒并增强生物防治潜力的可行性。

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