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口蹄疫病毒 SAT 血清型特异性 3ABC 检测方法的建立与验证,用于区分感染动物和免疫动物。

Development and validation of a foot-and-mouth disease virus SAT serotype-specific 3ABC assay to differentiate infected from vaccinated animals.

机构信息

Transboundary Animal Diseases, Onderstepoort Veterinary Institute, Agricultural Research Council, Private Bag X05, Onderstepoort, 0110, South Africa; Department of Microbiology and Plant Pathology, Faculty of Agricultural and Natural Sciences, University of Pretoria, Pretoria 0002, South Africa.

Istituto Zooprofilattico Sperimentale della Lombardia e dell'Emilia Romagna (IZSLER), Via Bianchi 7/9, 25124 Brescia, Italy.

出版信息

J Virol Methods. 2018 May;255:44-51. doi: 10.1016/j.jviromet.2018.02.006. Epub 2018 Feb 8.

Abstract

The effective control of foot-and-mouth disease (FMD) requires sensitive, specific and rapid diagnostic tools. However, the control and eradication of FMD in Africa is complicated by, among other factors, the existence of five of the seven FMD virus (FMDV) serotypes, including the SAT-serotypes 1, 2 and 3 that are genetically and antigenically the most variable FMDV serotypes. A key diagnostic assay to enable a country to re-gain its FMD-free status and for FMD surveillance, is the 3ABC or the non-structural protein (NSP) enzyme-linked immunosorbent assay (ELISA). Although many kits are available to detect 3ABC antibodies, none has been developed specifically for the variable SAT serotypes. This study designed a SAT-specific NSP ELISA and determined whether this assay could better detect NSP-specific antibodies from FMDV SAT-infected livestock. The assay's performance was compared to validated NSP assays (PrioCheck®-NSP and IZSLER-NSP), using panels of field and experimental sera, vaccinated and/or infected with FMDV SAT1, SAT2 or SAT3. The sensitivity () of the SAT-NSP was estimated as 76% (70%, 81%) whereas the specificity was 96% (95%, 98%) at a 95% confidence interval. The sensitivity and specificity were comparable to the commercial NSP assays, PrioCheck®-NSP (82% and 99%, respectively) and IZSLER-NSP (78% and 98%, respectively). Good correlations were observed for all three assays.

摘要

口蹄疫(FMD)的有效控制需要敏感、特异和快速的诊断工具。然而,非洲 FMD 的控制和根除工作因多种因素而变得复杂,其中包括存在 FMD 病毒(FMDV)的七个血清型中的五个,包括 SAT 血清型 1、2 和 3,它们在遗传和抗原性方面是最具变异性的 FMDV 血清型。使一个国家能够恢复无 FMD 状态并进行 FMD 监测的关键诊断检测方法是 3ABC 或非结构蛋白(NSP)酶联免疫吸附试验(ELISA)。尽管有许多试剂盒可用于检测 3ABC 抗体,但没有专门针对 SAT 血清型开发的试剂盒。本研究设计了一种 SAT 特异性 NSP ELISA,并确定该检测方法是否能够更好地检测 SAT 感染的 FMDV 牲畜的 NSP 特异性抗体。使用来自 FMDV SAT1、SAT2 或 SAT3 感染或接种疫苗的田间和实验血清的面板,比较了该检测方法与经过验证的 NSP 检测方法(PrioCheck®-NSP 和 IZSLER-NSP)的性能。SAT-NSP 的灵敏度()估计为 76%(70%,81%),特异性为 96%(95%,98%),置信区间为 95%。灵敏度和特异性与商业 NSP 检测方法相当,PrioCheck®-NSP(分别为 82%和 99%)和 IZSLER-NSP(分别为 78%和 98%)。所有三种检测方法都观察到良好的相关性。

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