Method: a single nucleotide polymorphism genotyping method for Wheat streak mosaic virus.

Stephanie M Rogers, Mark Payton, Robert W Allen, Ulrich Melcher, Jesse Carver, Jacqueline Fletcher
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Abstract

Background: The September 11, 2001 attacks on the World Trade Center and the Pentagon increased the concern about the potential for terrorist attacks on many vulnerable sectors of the US, including agriculture. The concentrated nature of crops, easily obtainable biological agents, and highly detrimental impacts make agroterrorism a potential threat. Although procedures for an effective criminal investigation and attribution following such an attack are available, important enhancements are still needed, one of which is the capability for fine discrimination among pathogen strains. The purpose of this study was to develop a molecular typing assay for use in a forensic investigation, using Wheat streak mosaic virus (WSMV) as a model plant virus.

Method: This genotyping technique utilizes single base primer extension to generate a genetic fingerprint. Fifteen single nucleotide polymorphisms (SNPs) within the coat protein and helper component-protease genes were selected as the genetic markers for this assay. Assay optimization and sensitivity testing was conducted using synthetic targets. WSMV strains and field isolates were collected from regions around the world and used to evaluate the assay for discrimination. The assay specificity was tested against a panel of near-neighbors consisting of genetic and environmental near-neighbors.

Result: Each WSMV strain or field isolate tested produced a unique SNP fingerprint, with the exception of three isolates collected within the same geographic location that produced indistinguishable fingerprints. The results were consistent among replicates, demonstrating the reproducibility of the assay. No SNP fingerprints were generated from organisms included in the near-neighbor panel, suggesting the assay is specific for WSMV. Using synthetic targets, a complete profile could be generated from as low as 7.15 fmoles of cDNA.

Conclusion: The molecular typing method presented is one tool that could be incorporated into the forensic science tool box after a thorough validation study. This method incorporates molecular biology techniques that are already well established in research and diagnostic laboratories, allowing for an easy introduction of this method into existing laboratories.

Keywords: single nucleotide polymorphisms, genotyping, plant pathology, viruses, microbial forensics, Single base primer extension, SNaPshot Multiplex Kit.

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Abstract Image

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方法:小麦条纹花叶病毒的单核苷酸多态性基因分型方法。
背景:2001 年 9 月 11 日对世界贸易中心和五角大楼的袭击使人们更加担心美国许多脆弱部门(包括农业)可能遭受恐怖袭击。农作物的集中性、生物制剂的易得性和严重的破坏性使农业恐怖主义成为一种潜在的威胁。虽然已经有了在此类袭击发生后进行有效刑事调查和归因的程序,但仍需要进行重要的改进,其中之一就是对病原体菌株进行精细分辨的能力。本研究的目的是以小麦条纹花叶病毒(WSMV)为植物病毒模型,开发一种用于法医调查的分子分型检测方法:这种基因分型技术利用单碱基引物延伸产生遗传指纹。方法:这种基因分型技术利用单碱基引物延伸产生遗传指纹,在衣壳蛋白和辅助成分蛋白酶基因中选择了 15 个单核苷酸多态性(SNPs)作为这种检测方法的遗传标记。使用合成靶标进行了测定优化和灵敏度测试。从世界各地收集了 WSMV 株系和田间分离物,用于评估该检测方法的鉴别能力。针对由遗传和环境近邻组成的近邻小组测试了该检测方法的特异性:结果:测试的每个 WSMV 株系或田间分离株都产生了独特的 SNP 指纹,只有在同一地理位置采集的三个分离株产生了无法区分的指纹。各重复样本的结果一致,证明了该检测方法的可重复性。近邻面板中的生物没有产生 SNP 指纹,这表明该检测方法对 WSMV 具有特异性。使用合成靶标,可以从低至 7.15 fmoles 的 cDNA 中生成完整的图谱:结论:所介绍的分子分型方法是一种经过全面验证研究后可纳入法医学工具箱的工具。该方法结合了在研究和诊断实验室中已经非常成熟的分子生物学技术,可以很容易地将该方法引入现有实验室中。关键词:单核苷酸多态性 基因分型 植物病理学 病毒 微生物法医学 单碱基引物延伸 SNaPshot多重试剂盒
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