首页> 外文期刊>Virus Research: An International Journal of Molecular and Cellular Virology >Complete genome sequence of virulent duck enteritis virus (DEV) strain 2085 and comparison with genome sequences of virulent and attenuated DEV strains.
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Complete genome sequence of virulent duck enteritis virus (DEV) strain 2085 and comparison with genome sequences of virulent and attenuated DEV strains.

机译:毒性鸭肠炎病毒(DEV)株2085的完整基因组序列,并与毒性和减毒DEV株的基因组序列进行比较。

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We here report the complete genome sequence of the duck enteritis virus (DEV) wild-type strain 2085, an avian herpesvirus (GenBank ID: JF999965). The nucleotide sequence was derived from the 2085 genome cloned as an infectious bacterial artificial chromosome (BAC) clone. The DEV 2085 genome is 160,649-bp in length and encodes 78 predicted open reading frames (ORFs), a number identical to that identified for the attenuated DEV VAC strain (GenBank ID: EU082088.2). Comparison of the genome sequences DEV 2085 and VAC with partial sequences of the virulent CHv strain and the attenuated strain Clone-03 was carried out to identify nucleotide or amino acid polymorphisms that potentially contribute to DEV virulence. No amino acid changes were identified in 24 of the 78 ORFs, a result indicating high conservation in DEV independently of strain origin or virulence. In addition, 39 ORFs contain non-synonymous nucleotide substitutions, while 15 ORFs had nucleotide insertions or deletions, frame-shift mutations and/or non-synonymous nucleotide substitutions with an effect on ORF initiation or termination. In 7 of the 15 ORFs with high and 27 of the 39 ORFs with low variability, polymorphisms were exclusively found in DEV 2085, a finding that likely is a result of a different origin of 2085 (Europe) or VAC, Clone-03 and CHv (Eastern Asia). Five ORFs (UL2, UL12, US10, UL47 and UL41) with polymorphisms were identical between the virulent DEV 2085 and CHv but different from VAC or Clone-03. They, individually or in combination, may therefore represent DEV virulence factors. Our comparative analysis of four DEV sequences provides a comprehensive overview of DEV genome structure and identifies ORFs that are changed during serial virus passage.
机译:我们在这里报告了鸭肠炎病毒(DEV)野生型菌株2085,禽疱疹病毒(GenBank ID:JF999965)的完整基因组序列。该核苷酸序列源自作为传染性细菌人工染色体(BAC)克隆而克隆的2085基因组。 DEV 2085基因组的长度为160,649-bp,编码78个预测的开放阅读框(ORF),该数目与针对DEV VAC减毒弱毒株(GenBank ID:EU082088.2)识别的数目相同。将基因组序列DEV 2085和VAC与强毒CHv株和减毒株Clone-03的部分序列进行比较,以鉴定可能有助于DEV毒力的核苷酸或氨基酸多态性。在78个ORF中有24个未发现氨基酸变化,结果表明DEV中的高保守性与菌株来源或毒力无关。此外,39个ORF包含非同义核苷酸取代,而15个ORF具有核苷酸插入或缺失,移码突变和/或非同义核苷酸取代,对ORF起始或终止产生影响。在高变异性的15个ORF中有7个,变异性低的39个ORF中有27个仅在DEV 2085中发现多态性,这一发现很可能是由于2085(欧洲)或VAC,Clone-03和CHv的来源不同(东亚)。有毒的DEV 2085和CHv之间有五个具有多态性的ORF(UL2,UL12,US10,UL47和UL41)相同,但不同于VAC或Clone-03。因此,它们单独或组合可以代表DEV毒力因子。我们对四个DEV序列的比较分析提供了DEV基因组结构的全面概述,并鉴定了在连续病毒传代过程中发生变化的ORF。

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