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从葱中快速高效浓缩甲型肝炎病毒方法的建立。

Development of a fast and efficient method for hepatitis A virus concentration from green onion.

机构信息

Northeast Regional Laboratory, Office of Regulatory Affairs, U.S. Food and Drug Administration, 158-15 Liberty Ave, Jamaica, NY 11433, USA.

Northeast Regional Laboratory, Office of Regulatory Affairs, U.S. Food and Drug Administration, 158-15 Liberty Ave, Jamaica, NY 11433, USA.

出版信息

J Virol Methods. 2017 Nov;249:161-164. doi: 10.1016/j.jviromet.2017.09.013. Epub 2017 Sep 14.

DOI:10.1016/j.jviromet.2017.09.013
PMID:28919035
Abstract

Hepatitis A virus (HAV) can cause serious liver disease and even death. HAV outbreaks are associated with the consumption of raw or minimally processed produce, making it a major public health concern. Infections have occurred despite the fact that effective HAV vaccine has been available. Development of a rapid and sensitive HAV detection method is necessary for an investigation of an HAV outbreak. Detection of HAV is complicated by the lack of a reliable culture method. In addition, due to the low infectious dose of HAV, these methods must be very sensitive. Current methods rely on efficient sample preparation and concentration steps followed by sensitive molecular detection techniques. Using green onions which was involved in most recent HAV outbreaks as a representative produce, a method of capturing virus particles was developed using carboxyl-derivatized magnetic beads in this study. Carboxyl beads, like antibody-coated beads or cationic beads, detect HAV at a level as low as 100 pfu/25g of green onions. RNA from virus concentrated in this manner can be released by heat-shock (98°C 5min) for molecular detection without sacrificing sensitivity. Bypassing the RNA extraction procedure saves time and removes multiple manipulation steps, which makes large scale HAV screening possible. In addition, the inclusion of beef extract and pectinase rather than NP40 in the elution buffer improved the HAV liberation from the food matrix over current methods by nearly 10 fold. The method proposed in this study provides a promising tool to improve food risk assessment and protect public health.

摘要

甲型肝炎病毒(HAV)可导致严重的肝脏疾病,甚至死亡。甲型肝炎病毒的爆发与食用生的或未经充分加工的农产品有关,因此成为主要的公共卫生关注点。尽管已有有效的 HAV 疫苗,但仍会发生感染。为了调查 HAV 爆发,需要开发一种快速、敏感的 HAV 检测方法。由于缺乏可靠的培养方法,HAV 的检测较为复杂。此外,由于 HAV 的感染剂量较低,这些方法必须非常敏感。目前的方法依赖于高效的样品制备和浓缩步骤,然后是敏感的分子检测技术。

本研究以最近几次 HAV 爆发中涉及的大葱为代表农产品,开发了一种使用羧基衍生磁珠捕获病毒颗粒的方法。羧基珠,如抗体包被珠或阳离子珠,可以检测到低至 100 pfu/25g 大葱的 HAV。以这种方式浓缩的 RNA 可以通过热休克(98°C 5min)释放用于分子检测,而不会牺牲灵敏度。省略 RNA 提取步骤可节省时间并减少多个操作步骤,从而实现大规模的 HAV 筛选。此外,在洗脱缓冲液中加入牛肉提取物和果胶酶而不是 NP40,可使从食品基质中释放 HAV 的效率比目前的方法提高近 10 倍。

本研究提出的方法为改善食品风险评估和保护公众健康提供了有前途的工具。

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