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Two novel mitoviruses from a Canadian isolate of the Dutch elm pathogen Ophiostoma novo-ulmi (93–1224)

机译:来自加拿大榆树病原体Ophiostoma novo-ulmi的加拿大分离株的两种新型线粒病毒(93-1224)

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Background Ophiostoma novo-ulmi is the causative agent of Dutch elm disease (DED). It is an ascomycetous filamentous fungus that ranks as the third most devastating fungal pathogen in Canada. The disease front has spread eastward and westward from the epicentre in Ontario and Quebec and is threatening elm populations across the country. Numerous mitigation strategies have been tried to eradicate this pathogen, but success has thus far been limited. An alternative approach might utilize double-stranded RNA (dsRNA) mycoviruses which have been reported to induce hypovirulence in other fungi. Methods Using a modified single primer amplification technique (SPAT) in combination with chromosomal walking, we have determined the genome sequence of two RdRp encoding dsRNA viruses from an O. novo-ulmi isolate (93–1224) collected from the disease front in Winnipeg. Results We propose that these viruses, which we have named OnuMV1c and OnuMV7 based on sequence similarity to other Ophiostoma mitoviruses, are two new members of the genus Mitovirus in the family Narnaviridae. Conclusions The discovery of such dsRNA elements raises the potential for engineering these viruses to include other genetic elements, such as anti-sense or interfering RNAs, to create novel and highly specific biological controls. Na?ve fungal hosts could be infected with both the engineered molecule and a helper mitovirus encoding an RdRp which would provide replication capacity for both molecules.
机译:背景新蛇眼石是荷兰榆病(DED)的病原体。它是一种子囊菌丝状真菌,在加拿大排名第三,是最具破坏力的真菌病原体。疾病前沿从安大略和魁北克的震中向东和向西扩散,并威胁着全国的榆树种群。已经尝试了多种缓解策略来根除这种病原体,但是迄今为止,成功的方法是有限的。另一种方法可能是利用双链RNA(dsRNA)分支杆菌病毒,据报道该病毒可诱导其他真菌的低毒力。方法通过使用改良的单引物扩增技术(SPAT)结合染色体行走,我们从温尼伯疾病前沿收集的O. noul-ulmi分离株(93-1224)中确定了两种编码dsRNA病毒的RdRp的基因组序列。结果我们提出,这些病毒根据与其他蛇口鱼线粒体病毒的序列相似性而被命名为OnuMV1c和OnuMV7,是鼻病毒科中线粒体病毒属的两个新成员。结论此类dsRNA元件的发现提高了对这些病毒进行工程改造以使其包含其他遗传元件(例如反义或干扰RNA)的潜力,从而创造出新颖且高度特异性的生物学控制。初生真菌宿主可能同时感染了工程化分子和编码RdRp的辅助线粒体病毒,后者可为两个分子提供复制能力。

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