首页> 外文期刊>International Journal of Hygiene and Environmental Health >Reverse transcription-quantitative PCR assays for genotype-specific detection of human noroviruses in clinical and environmental samples
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Reverse transcription-quantitative PCR assays for genotype-specific detection of human noroviruses in clinical and environmental samples

机译:用于临床和环境样品中人类诺如病毒基因型特异性检测的逆转录定量PCR分析

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摘要

Circulation of human noroviruses in water environments is suspected to be genotype-dependent, but the established primer and probe sets for noroviruses are usually genogroup-specific, which do not allow to compare the genotype-specific properties, such as persistence in water environments and resistance to disinfectants. In this study, quantitative PCR assays were designed for genotype-specific quantification of four epidemiologically important genotypes, GII.3, GII.4, GII.6, and GII.17. Developed assays were tested using norovirus positive stool samples which were previously confirmed to present target genotypes of this study. The results were 100% in accordance with the previous results. Effect of the co-existence of multiple genotypes in a sample on the target genotype quantification was evaluated using composite stool samples and wastewater samples containing multiple genotypes and the presence of non-target genotypes didn't affect the quantification of target genotype. Sensitivity and specificity was 100% for all four assays developed in this study with no cross-reactions between genotypes demonstrating the validity of our assays and their applicability to clinical and environmental samples.
机译:人类诺如病毒在水环境中的传播被怀疑是基因型依赖性的,但是已建立的诺如病毒的引物和探针组通常是基因组特异性的,因此不允许比较基因型特异性的特性,例如在水环境中的持久性和耐药性消毒剂。在本研究中,设计了定量PCR分析方法,用于对四种流行病学上重要的基因型GII.3,GII.4,GII.6和GII.17进行基因型特异性定量。使用诺如病毒阳性粪便样本测试了开发的检测方法,这些样本先前已被证实具有本研究的靶基因型。结果是100%与以前的结果一致。使用复合粪便样品和包含多种基因型的废水样品,评估了样品中多种基因型共存对目标基因型定量的影响,并且非目标基因型的存在不影响目标基因型的定量。在这项研究中开发的所有四种测定的敏感性和特异性均为100%,基因型之间没有交叉反应,这证明了我们测定的有效性以及它们在临床和环境样品中的适用性。

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  • 作者单位

    Tohoku Univ, Gradual Sch Engn, Dept Civil & Environm Engn, Aoba Ku, 6-6-06 Aoba, Sendai, Miyagi 9808579, Japan;

    Hokkaido Univ, Fac Engn, Div Environm Engn, Kita Ku, North 13,West 8, Sapporo, Hokkaido 0608628, Japan;

    Hokkaido Univ, Fac Engn, Div Environm Engn, Kita Ku, North 13,West 8, Sapporo, Hokkaido 0608628, Japan;

    Inst Super Tecn, Lab Anal, Av Rovisco Pais, P-1049001 Lisbon, Portugal;

    Inst Super Tecn, Lab Anal, Av Rovisco Pais, P-1049001 Lisbon, Portugal;

    Natl Inst Publ Hlth, Dept Environm Hlth, 2-3-6 Minami, Wako, Saitama 3510197, Japan;

    Ochanomizu Univ, Ctr Simulat Sci & Informat Biol, Bunkyo Ku, 2-1-1 Otsuka, Tokyo 1128610, Japan;

    Hokkaido Univ, Fac Engn, Div Environm Engn, Kita Ku, North 13,West 8, Sapporo, Hokkaido 0608628, Japan;

    Tohoku Univ, Gradual Sch Engn, Dept Civil & Environm Engn, Aoba Ku, 6-6-06 Aoba, Sendai, Miyagi 9808579, Japan;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Norovirus; Quantification; Genotype; RT-qPCR; Primers; Monitoring;

    机译:诺如病毒;定量;基因型;RT-qPCR;引物;监测;
  • 入库时间 2022-08-18 03:47:52

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