首页> 外文期刊>Journal of Virological Methods >Improved PCR diagnostics using up-to-date in silico validation: An F-gene RT-qPCR assay for the detection of all four lineages of peste des petits ruminants virus
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Improved PCR diagnostics using up-to-date in silico validation: An F-gene RT-qPCR assay for the detection of all four lineages of peste des petits ruminants virus

机译:使用硅验证的最新改进PCR诊断:用于检测Peste Des Petits反刍动物病毒的所有四个谱系的F-GeneTT-QPCR测定

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摘要

Peste des petits ruminants (PPR) is a globally significant disease of small ruminants caused by the peste des petits ruminants virus (PPRV) that is considered for eradication by 2030 by the United Nations Food and Agriculture Organisation (FAO). Critical to the eradication of PPR are accurate diagnostic assays. RT-qPCR assays targeting the nucleocapsid gene of PPRV have been successfully used for the diagnosis of PPR. We describe the development of an RT-qPCR assay targeting an alternative region (the fusion (F) gene) based on the most up-to-date PPRV sequence data. In silica analysis of the F-gene RT-qPCR assay performed using PCRv software indicated 98% sensitivity and 100% specificity against all PPRV sequences published in Genbank. The assay indicated the greatest in silico sensitivity in comparison to other previously published and recommended PPRV RT-qPCR assays. We evaluated the assay using strains representative of all 4 lineages in addition to samples obtained from naturally and experimentally-infected animals. The F-gene RT-qPCR assay showed 100% diagnostic specificity and demonstrated a limit of detection of 10 PPRV genome copies per mu l. This RT-qPCR assay can be used in isolation or in conjunction with other assays for confirmation of PPR and should support the global efforts for eradication.
机译:Peste des Petits反刍动物(PPR)是由Peste Des Petits反刍动物病毒(PPRV)引起的小型反刍动物的全球性显着性疾病,该病毒(PPRV)被联合国粮食和农业组织(粮农组织)在2030年被灭绝。对消除PPR至关重要的是准确的诊断测定。靶向PPRV的核衣壳基因的RT-QPCR测定已成功用于PPR的诊断。我们描述了靶向替代区域(融合(F)基因)的RT-QPCR测定的发展,基于最新的PPRV序列数据。在使用PCRV软件进行的F-GeneTTR-QPCR测定的二氧化硅分析中,指示Genbank中发表的所有PPRV序列的98%敏感性和100%的特异性。与其他先前发表的和推荐的PPRV RT-QPCR测定相比,该测定表明了硅敏感性最大。除了从自然和实验感染的动物获得的样品之外,我们使用所有4种谱系的菌株评估了测定。 F-GeneTTT-QPCR测定显示100%诊断特异性,并证明了每亩L的10个PPRV基因组拷贝的检测限。该RT-QPCR测定可用于分离或与其他测定结合使用以确认PPR,并应支持全球根除努力。

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