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检测猪胃黏膜黏附磁珠从冷冻浆果中提取诺如病毒的效率。

Examining the efficiency of porcine gastric mucin-coated magnetic beads in extraction of noroviruses from frozen berries.

机构信息

Microbiology Laboratory, Regulatory Operations and Enforcement Branch, Health Canada, 1001 St-Laurent Street West, Longueuil, QC, J4K 1C7, Canada.

National Food Virology Reference Centre, Bureau of Microbial Hazards, Food Directorate, Health Canada, 251 Sir Frederick Banting Driveway, Ottawa, ON, K1A 0K9, Canada.

出版信息

Food Microbiol. 2024 Jun;120:104461. doi: 10.1016/j.fm.2023.104461. Epub 2023 Dec 29.

Abstract

Human norovirus is the leading cause of foodborne gastroenteritis worldwide. Due to the low infectious dose of noroviruses, sensitive methodologies are required to detect and characterize small numbers of viral particles that are found in contaminated foods. The ISO 15216 method, which is internationally recognized for detection of foodborne viruses from high-risk food commodities, is based on viral precipitation, followed by RNA extraction and identification of the viral genome by RT-PCR. Although the ISO 15216 method is efficient, it is time consuming and tedious, does not report on the viral infectivity, and is sensitive to the presence of RT-PCR inhibitors. Norovirus capture by the porcine gastric mucin conjugated magnetic beads (PGM-MB) was developed as an alternative virus recovery method. It relies on the integrity of the viral capsid being able to bind to PGM. PGM contains a variety of histo-blood group antigens (HBGAs) that act as norovirus receptors. Therefore, the PGM-MB method allows for extraction of noroviruses, with potentially intact viral capsids, from complex food matrices. The viral genome can then be released through heat-shock of the captured virus. For this reason, we performed a parallel comparison between the ISO 15216 method and the PGM-MB method in isolation and quantification of noroviruses from frozen raspberries. We have demonstrated that the efficiency of the PGM-MB method in extraction of murine norovirus (MNV) and human norovirus GII.4 from raspberries is equal or better than the ISO 15216 method, while the PGM-MB has fewer steps and shorter turnaround time. Moreover, the PGM-MB method is more efficient in removing the inhibitors prior to RT-PCR analysis.

摘要

人诺如病毒是全球食源性胃肠炎的主要原因。由于诺如病毒的感染剂量低,因此需要敏感的方法来检测和表征污染食品中发现的少量病毒颗粒。国际上公认的用于检测高危食品中食源病毒的 ISO 15216 方法基于病毒沉淀,然后进行 RNA 提取,并通过 RT-PCR 鉴定病毒基因组。尽管 ISO 15216 方法效率高,但耗时繁琐,不报告病毒感染力,并且对 RT-PCR 抑制剂敏感。猪胃粘蛋白偶联磁珠(PGM-MB)捕获诺如病毒是作为替代病毒回收方法而开发的。它依赖于病毒衣壳的完整性能够与 PGM 结合。PGM 含有多种组织血型抗原(HBGAs),可作为诺如病毒的受体。因此,PGM-MB 方法允许从复杂的食物基质中提取具有潜在完整病毒衣壳的诺如病毒。然后可以通过热休克释放捕获的病毒中的基因组。因此,我们在从冷冻覆盆子中分离和定量诺如病毒方面对 ISO 15216 方法和 PGM-MB 方法进行了平行比较。我们已经证明,PGM-MB 方法从覆盆子中提取鼠诺如病毒(MNV)和人诺如病毒 GII.4 的效率与 ISO 15216 方法相当或更好,而 PGM-MB 方法的步骤更少,周转时间更短。此外,PGM-MB 方法在 RT-PCR 分析之前更有效地去除抑制剂。

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