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利用携带小报告标签的重组瘟病毒开发高通量血清中和试验

Development of a High-Throughput Serum Neutralization Test Using Recombinant Pestiviruses Possessing a Small Reporter Tag.

作者信息

Tetsuo Madoka, Matsuno Keita, Tamura Tomokazu, Fukuhara Takasuke, Kim Taksoo, Okamatsu Masatoshi, Tautz Norbert, Matsuura Yoshiharu, Sakoda Yoshihiro

机构信息

Laboratory of Microbiology, Division of Disease Control, Faculty of Veterinary Medicine, Hokkaido University, Sapporo, Hokkaido 060-0818, Japan.

Global Station for Zoonosis Control, Global Institute for Collaborative Research and Education (GI-CoRE), Hokkaido University, Sapporo 001-0020, Japan.

出版信息

Pathogens. 2020 Mar 4;9(3):188. doi: 10.3390/pathogens9030188.

Abstract

A serum neutralization test (SNT) is an essential method for the serological diagnosis of pestivirus infections, including classical swine fever, because of the cross reactivity of antibodies against pestiviruses and the non-quantitative properties of antibodies in an enzyme-linked immunosorbent assay. In conventional SNTs, an immunoperoxidase assay or observation of cytopathic effect after incubation for 3 to 7 days is needed to determine the SNT titer, which requires labor-intensive or time-consuming procedures. Therefore, a new SNT, based on the luciferase system and using classical swine fever virus, bovine viral diarrhea virus, and border disease virus possessing the 11-amino-acid subunit derived from NanoLuc luciferase was developed and evaluated; this approach enabled the rapid and easy determination of the SNT titer using a luminometer. In the new method, SNT titers can be determined tentatively at 2 days post-infection (dpi) and are comparable to those obtained by conventional SNTs at 3 or 4 dpi. In conclusion, the luciferase-based SNT can replace conventional SNTs as a high-throughput antibody test for pestivirus infections.

摘要

血清中和试验(SNT)是瘟病毒感染血清学诊断的重要方法,包括经典猪瘟,这是由于针对瘟病毒的抗体具有交叉反应性,以及酶联免疫吸附试验中抗体的非定量特性。在传统的SNT中,需要进行免疫过氧化物酶试验或在孵育3至7天后观察细胞病变效应来确定SNT滴度,这需要耗费大量人力或时间的程序。因此,开发并评估了一种基于荧光素酶系统的新型SNT,该系统使用具有源自纳米荧光素酶的11个氨基酸亚基的经典猪瘟病毒、牛病毒性腹泻病毒和边界病病毒;这种方法能够使用发光计快速简便地确定SNT滴度。在新方法中,感染后2天(dpi)即可初步确定SNT滴度,且与传统SNT在3或4 dpi时获得的滴度相当。总之,基于荧光素酶的SNT可替代传统SNT,作为瘟病毒感染的高通量抗体检测方法。

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