Enteric, Environmental and Food Virology Laboratory, Institute of Environmental Science and Research Ltd (ESR), Kenepuru Science Centre, PO BOX 50-348, Porirua, 5240, New Zealand.
Food Environ Virol. 2018 Jun;10(2):151-158. doi: 10.1007/s12560-018-9336-6. Epub 2018 Feb 7.
Norovirus outbreaks are associated with the consumption of contaminated shellfish, and so efficient methods to recover and detect infectious norovirus in shellfish are important. The Proteinase K digestion method used to recover norovirus from shellfish, as described in the ISO 15216, would be a good candidate but its impact on the virus capsid integrity and thus infectivity was never examined. The aim of this study was to assess the impact of the Proteinase K digestion method, and of the heat treatment component of the method alone, on norovirus (genogroups I and II) and MS2 bacteriophage capsid integrity. A slightly modified version of the ISO method was used. RT-qPCR was used for virus detection following digestion of accessible viral RNA using RNases. MS2 phage infectivity was measured using a plaque assay. The effect of shellfish digestive glands (DG) on recovery was evaluated. In the presence of shellfish DG, a reduction in MS2 phage infectivity of about 1 log was observed after the Proteinase K digestion method and after heat treatment component alone. For norovirus GII and MS2 phage, there was no significant loss of genome following the Proteinase K digestion method but there was a significant 0.24 log loss of norovirus GI. In the absence of shellfish DG, the reduction in MS2 phage infectivity was about 2 log, with the addition of RNases resulting in a significant loss of genome for all tested viruses following complete Proteinase K digestion method and the heat treatment alone. While some protective effect from the shellfish DG on viruses was observed, the impact on capsid integrity and infectivity suggests that this method, while suitable for norovirus genome detection, may not completely preserve virus infectivity.
诺如病毒暴发与食用受污染的贝类有关,因此,高效的方法来回收和检测贝类中的传染性诺如病毒非常重要。ISO 15216 中描述的从贝类中回收诺如病毒的蛋白酶 K 消化方法是一个很好的候选方法,但从未检查过该方法对病毒衣壳完整性的影响,以及对病毒感染性的影响。本研究的目的是评估蛋白酶 K 消化方法,以及该方法的热处理成分单独对诺如病毒(基因组 I 和 II)和 MS2 噬菌体衣壳完整性的影响。使用稍作修改的 ISO 方法。在使用 RNases 消化可访问的病毒 RNA 后,使用 RT-qPCR 进行病毒检测。使用噬菌斑测定法测量 MS2 噬菌体的感染性。评估贝类消化腺(DG)对回收的影响。在存在贝类 DG 的情况下,蛋白酶 K 消化方法和单独的热处理成分后,MS2 噬菌体的感染性降低了约 1 个对数级。对于诺如病毒 GII 和 MS2 噬菌体,蛋白酶 K 消化方法后基因组没有明显丢失,但 GI 型诺如病毒的丢失量明显为 0.24 个对数级。在不存在贝类 DG 的情况下,MS2 噬菌体的感染性降低了约 2 个对数级,添加 RNases 后,在完全蛋白酶 K 消化方法和单独的热处理后,所有测试病毒的基因组都明显丢失。虽然观察到贝类 DG 对病毒有一定的保护作用,但对衣壳完整性和感染性的影响表明,该方法虽然适合诺如病毒基因组检测,但可能无法完全保留病毒的感染性。