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用于检测非洲猪瘟病毒pp62蛋白特异性抗体的间接酶联免疫吸附测定法的开发。

Development of an Indirect ELISA to Detect African Swine Fever Virus pp62 Protein-Specific Antibodies.

作者信息

Zhong Kexin, Zhu Mengmeng, Yuan Qichao, Deng Zhibang, Feng Simeng, Liu Daoxin, Yuan Xiaomin

机构信息

Lab of Animal Disease Prevention and Control and Animal Model, Hunan Provincial Key Laboratory of Protein Engineering in Animal Vaccines, College of Veterinary Medicine, Hunan Agricultural University (HUNAU), Changsha, China.

Animal Disease Prevention and Control Center, Changsha, China.

出版信息

Front Vet Sci. 2022 Jan 13;8:798559. doi: 10.3389/fvets.2021.798559. eCollection 2021.

Abstract

African swine fever (ASF) is a highly detrimental viral disease caused by African swine fever virus (ASFV). The occurrence and prevalence of this disease have become a serious threat to the global swine industry and national economies. At present, the detection volume of African swine fever is huge, more sensitive and accurate detection techniques are needed for the market. pp62 protein, as a protein in the late stage of infection, has strong antigenicity and a high corresponding antibody titer in infected pigs. In this study, the CP530R gene was cloned into expression vector pET-28a to construct a prokaryotic expression plasmid, which was induced by IPTG to express soluble pp62 protein. Western blot analysis showed that it had great reactivity. Using the purified recombinant protein as an antigen, an indirect ELISA method for detecting ASFV antibody was established. The method was specific only to ASFV-positive serum, 1:1600 diluted positive serum could still be detected, and the coefficients of variation (CV) of the intra assay and inter assay were both <10%. It turns out that the assays had excellent specificity, sensitivity, and repeatability. This provides an accurate, rapid, and economical method for the detection of ASFV antibody in clinical pig serum samples.

摘要

非洲猪瘟(ASF)是由非洲猪瘟病毒(ASFV)引起的一种极具危害性的病毒性疾病。该疾病的发生和流行已对全球养猪业和国家经济构成严重威胁。目前,非洲猪瘟的检测量巨大,市场需要更灵敏、准确的检测技术。pp62蛋白作为感染后期的一种蛋白,具有很强的抗原性,且在感染猪体内有较高的相应抗体效价。在本研究中,将CP530R基因克隆到表达载体pET-28a中构建原核表达质粒,经异丙基-β-D-硫代半乳糖苷(IPTG)诱导表达可溶性pp62蛋白。蛋白质免疫印迹分析表明其具有很强的反应活性。以纯化的重组蛋白为抗原,建立了一种检测ASFV抗体的间接酶联免疫吸附测定(ELISA)方法。该方法仅对ASFV阳性血清具有特异性,1:1600稀释的阳性血清仍可被检测到,批内和批间变异系数(CV)均<10%。结果表明该检测方法具有优异的特异性、敏感性和重复性。这为临床猪血清样本中ASFV抗体的检测提供了一种准确、快速且经济的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c84/8792508/f83ddbd85d78/fvets-08-798559-g0001.jpg

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