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衣壳和基因组完整性测试对诺如病毒提取回收率的影响

Impact of Capsid and Genomic Integrity Tests on Norovirus Extraction Recovery Rates.

作者信息

Raymond Philippe, Paul Sylvianne, Guy Rebecca A

机构信息

St-Hyacinthe Laboratory-Food Virology, Canadian Food Inspection Agency (CFIA), St-Hyacinthe, QC J2S 8E3, Canada.

National Microbiology Laboratory, Division of Enteric Diseases, Public Health Agency of Canada (PHAC), Guelph, ON N1G 3W4, Canada.

出版信息

Foods. 2023 Feb 15;12(4):826. doi: 10.3390/foods12040826.

DOI:10.3390/foods12040826
PMID:36832901
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9957022/
Abstract

Human norovirus (HuNoV) is the leading pathogen responsible for food-borne illnesses. However, both infectious and non-infectious HuNoV can be detected by RT-qPCR. This study evaluated the efficiency of different capsid integrity treatments coupled with RT-qPCR or a long-range viral RNA (long RT-qPCR) detection to reduce the recovery rates of heat inactivated noroviruses and fragmented RNA. The three capsid treatments evaluated (RNase, the intercalating agent PMAxx and PtCl) reduced the recovery of heat inactivated HuNoV and murine norovirus (MNV) spiked on lettuce, when combined with the ISO 15216-1:2017 extraction protocols. However, PtCl also reduced non-heat-treated noroviruses recovery as estimated by RT-qPCR. The PMAxx and RNase treatments had a similar effect on MNV only. The most efficient approaches, the RNase and PMAxx treatments, reduced the heat-inactivated HuNoV recovery rates estimated using RT-qPCR by 2 and >3 log, respectively. The long RT-qPCR detection approach also reduced the recovery rates of heat inactivated HuNoV and MNV by 1.0 and 0.5 log, respectively. Since the long-range viral RNA amplification could be applied to verify or confirm RT-qPCR results, it also provides some advantages by reducing the risk of false positive HuNoV results.

摘要

人诺如病毒(HuNoV)是食源性疾病的主要病原体。然而,传染性和非传染性HuNoV均可通过逆转录定量聚合酶链反应(RT-qPCR)检测到。本研究评估了不同衣壳完整性处理方法结合RT-qPCR或长程病毒RNA(长程RT-qPCR)检测,以降低热灭活诺如病毒和片段化RNA回收率的效果。评估的三种衣壳处理方法(核糖核酸酶、嵌入剂PMAxx和氯化铂)与ISO 15216-1:2017提取方案联合使用时,可降低接种在生菜上的热灭活HuNoV和鼠诺如病毒(MNV)的回收率。然而,氯化铂也降低了RT-qPCR估计的未经热处理的诺如病毒回收率。PMAxx和核糖核酸酶处理仅对MNV有类似效果。最有效的方法,即核糖核酸酶和PMAxx处理,分别将使用RT-qPCR估计的热灭活HuNoV回收率降低了2个对数和大于3个对数。长程RT-qPCR检测方法也分别将热灭活HuNoV和MNV的回收率降低了1.0个对数和0.5个对数。由于长程病毒RNA扩增可用于验证或确认RT-qPCR结果,通过降低HuNoV假阳性结果的风险,它也具有一些优势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ed4/9957022/c86dada369d8/foods-12-00826-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ed4/9957022/5a9e8c263814/foods-12-00826-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ed4/9957022/c86dada369d8/foods-12-00826-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ed4/9957022/5a9e8c263814/foods-12-00826-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ed4/9957022/c86dada369d8/foods-12-00826-g002.jpg

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