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A fast and robust method for whole genome sequencing of the Aleutian Mink Disease Virus (AMDV) genome

机译:一种快速而稳健的阿留申水貂病病毒(amDV)基因组全基因组测序方法

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摘要

Aleutian Mink Disease Virus (AMDV) is a frequently encountered pathogen associated with commercial mink breeding. AMDV infection leads to increased mortality and compromised animal health and welfare. Currently little is known about the molecular evolution of the virus, and the few existing studies have focused on limited regions of the viral genome. This paper describes a robust, reliable, and fast protocol for amplification of the full AMDV genome using long-range PCR. The method was used to generate next generation sequencing data for the non-virulent cell-culture adapted AMDV-G strain as well as for the virulent AMDV-Utah strain. Comparisons at nucleotide- and amino acid level showed that, in agreement with existing literature, the highest variability between the two virus strains was found in the left open reading frame, which encodes the non-structural (NS1–3) genes. This paper also reports a number of differences that potentially can be linked to virulence and host range. To the authors’ knowledge, this is the first study to apply next generation sequencing on the entire AMDV genome. The results from the study will facilitate the development of new diagnostic tools and can form the basis for more detailed molecular epidemiological analyses of the virus.
机译:阿留申水貂病病毒(AMDV)是与商业水貂育种相关的常见病原体。 AMDV感染导致死亡率增加,动物健康和福利受损。目前对该病毒的分子进化知之甚少,而现有的研究很少集中在病毒基因组的有限区域。本文介绍了使用远程PCR扩增完整AMDV基因组的可靠,可靠和快速的协议。该方法用于为适应非毒力细胞培养的AMDV-G菌株以及有毒的AMDV-Utah菌株生成下一代测序数据。在核苷酸和氨基酸水平上的比较表明,与现有文献一致,这两个病毒株之间的最大变异性出现在左侧的开放阅读框内,该框编码非结构性(NS1-3)基因。本文还报告了许多可能与毒力和寄主范围有关的差异。据作者所知,这是第一项将下一代测序应用于整个AMDV基因组的研究。该研究的结果将有助于开发新的诊断工具,并可为对该病毒进行更详细的分子流行病学分析奠定基础。

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