首页> 外文期刊>Acta Veterinaria Hungarica >Development of a novel immunoperoxidase monolayer assay for detection of swine hepatitis E virus antibodies based on stable cell lines expressing the ORF3 protein.
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Development of a novel immunoperoxidase monolayer assay for detection of swine hepatitis E virus antibodies based on stable cell lines expressing the ORF3 protein.

机译:基于表达ORF3蛋白的稳定细胞系,开发了一种新型免疫过氧化物酶单层测定方法,用于检测猪戊型肝炎病毒抗体。

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摘要

Hepatitis E virus (HEV) strains are classified into 4 genotypes by nucleotide sequencing. Genotypes 3 and 4 infect humans and animals via HEV-contaminated food or water. HEV RNA was detected by PCR and antibodies were detected by ELISA. Since human studies showed that HEV IgG antibodies in sera can persist for extended periods, diagnosis of HEV infection in swine or humans is mainly based on serological detection using commercial ELISA kits. However, there is no supplemental method to verify ELISA results. Hence, we developed a novel method used for mutual correction of these common processes. Here, a modified stable HepG2 cell line was transfected with pcDNA3.1-ORF3 to express the swine HEV ORF3 protein. Based on this cell line, a novel immunoperoxidase monolayer assay (IPMA) was developed to detect antibodies against HEV. The results show that this method has good specificity, sensitivity and repeatability. When used to investigate 141 porcine serum samples, the IPMA had a coincidence rate of 92.2% with a commercial ELISA kit. The established IPMA described herein is valuable as a supplemental method to ELISA and can differentiate infections by HEV and other viruses.
机译:戊型肝炎病毒(HEV)菌株通过核苷酸测序分为4个基因型。基因型3和4通过HEV污染的食物或水感染人类和动物。通过PCR检测HEV RNA,通过ELISA检测抗体。由于人类研究表明,血清中的HEV IgG抗体可以长期存在,因此诊断猪或人类HEV感染主要是基于使用商业ELISA试剂盒的血清学检测。但是,没有补充方法可以验证ELISA结果。因此,我们开发了一种用于相互纠正这些常见过程的新颖方法。在这里,用pcDNA3.1-ORF3转染了修饰的稳定的HepG2细胞系,以表达猪HEV ORF3蛋白。基于该细胞系,开发了一种新型的免疫过氧化物酶单层测定(IPMA),以检测抗HEV的抗体。结果表明,该方法具有良好的特异性,灵敏度和重复性。当用于调查141份猪血清样本时,IPMA与商用ELISA试剂盒的符合率为92.2%。本文描述的已建立的IPMA作为ELISA的补充方法很有价值,并且可以区分HEV和其他病毒的感染。

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