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首页> 外文期刊>Canadian Journal of Plant Pathology: Revue Canadienne de phytopathologie >Molecular characterization of Potato mop-top virus isolates from China and Canada and development of RT-PCR differentiation of two sequence variant groups
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Molecular characterization of Potato mop-top virus isolates from China and Canada and development of RT-PCR differentiation of two sequence variant groups

机译:来自中国和加拿大的马铃薯拖把病毒分离株的分子表征和两个序列变异组的RT-PCR分化发展

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摘要

The complete genome comprising three genomic RNAs of three Canadian and two Chinese isolates of Potato mop-top virus were sequenced and analysed. Two open reading frames (ORFs) were found in RNA1 of 6.1 kb, encoding a readthrough RNA-dependent RNA polymerase (RdRp). A coat protein (CP)-readthrough protein was encoded by RNA2 of 3.1 kb. Four ORFs that encoded the triple gene block proteins (TGBps) and a cysteine-rich protein were found in RNA3 (2.9 kb) of the Chinese isolate 'Yunnan'; whereas in the remaining isolates (three Canadian isolates and the Chinese isolate 'Guangdong'), only three ORFs encoding TGBps were observed in RNA3. A single nucleotide mutation of A(2462) to G(2462) abolished the start codon 'AUG' for the fourth putative ORF in RNA3 of these isolates. Based on phylogenetic and sequence similarity analysis of these isolates as well as those reported by others at the complete RNA sequence level, each of RNA1, RNA2 and RNA3 could be divided into at least two groups. In Canadian isolates 'Ch9', 'Ch10' and 'Ch20' and Chinese isolate 'Guangdong', all genomic RNAs belonged to group A; and in Chinese isolate 'Yunnan', all of its RNA belonged to group B. Interestingly, in Swedish isolate 'Sw', RNA1 and RNA2 belonged to group A while RNA3 belonged to group B. A duplex RT-PCR for differentiating groups A and B of RNA3 was developed and evaluated. All PMTV samples collected in Guangdong, China, and New Brunswick, Canada, possessed a RNA3 belonging to group A; whereas the samples collected in Yunnan, China, possessed a RNA3 belonging to group B.
机译:完整的基因组由三个加拿大的马铃薯和两个中国分离的马铃薯拖把病毒的三个基因组RNA组成,并进行了测序和分析。在6.1 kb的RNA1中发现了两个开放阅读框(ORF),编码一个依赖于阅读的RNA依赖性RNA聚合酶(RdRp)。外壳蛋白(CP)通读蛋白由3.1 kb的RNA2编码。在中国分离株“云南”的RNA3(2.9 kb)中发现了四个编码三重基因阻断蛋白(TGBps)和富含半胱氨酸蛋白的ORF。而在其余的分离株中(三个加拿大分离株和中国分离株“广东”),在RNA3中仅观察到三个编码TGBps的ORF。 A(2462)到G(2462)的单核苷酸突变消除了这些分离株RNA3中第四个推定ORF的起始密码子'AUG'。基于这些分离株的系统发育和序列相似性分析以及其他分离株在完整RNA序列水平上的报道,RNA1,RNA2和RNA3至少可以分为两组。在加拿大的“ Ch9”,“ Ch10”和“ Ch20”分离株以及中国的“广东”分离株中,所有基因组RNA均属于A组。有趣的是,在瑞典分离株“ Sw”中,RNA1和RNA2属于A组,而RNA3属于B组。用于区分A和A组的双工RT-PCR开发并评估了RNA3B。在中国广东省和加拿大新不伦瑞克省采集的所有PMTV样品均具有属于A组的RNA3。而在中国云南采集的样本具有属于B组的RNA3。

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