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一种用于检测猪流行性腹泻病毒抗原的新型双抗体夹心定量酶联免疫吸附测定法的开发。

Development of a Novel Double Antibody Sandwich Quantitative Enzyme-Linked Immunosorbent Assay for Detection of Porcine Epidemic Diarrhea Virus Antigen.

作者信息

Fan Baochao, Sun Jie, Zhu Lin, Zhou Jinzhu, Zhao Yongxiang, Yu Zhengyu, Sun Bing, Guo Rongli, He Kongwang, Li Bin

机构信息

Key Laboratory of Veterinary Biological Engineering and Technology Ministry of Agriculture, Institute of Veterinary Medicine, Jiangsu Academy of Agricultural Sciences, Nanjing, China.

Jiangsu Key Laboratory for Food Quality and Safety-State Key Laboratory Cultivation Base of Ministry of Science and Technology, Nanjing, China.

出版信息

Front Vet Sci. 2020 Oct 26;7:540248. doi: 10.3389/fvets.2020.540248. eCollection 2020.

Abstract

Porcine epidemic diarrhea virus (PEDV) causes acute diarrhea and dehydration in sucking piglets with a high mortality rate. Here, we developed a double antibody sandwich quantitative enzyme-linked immunosorbent assay (DAS-qELISA) for detection of PEDV using a specific monoclonal antibody against PEDV N protein and anti-PEDV rabbit serum. Using DAS-qELISA, the detection limit of recombinant PEDV N protein and virus titer were approximately 1 μg/L and 10 TCID/ml, respectively. A total of 90 intestinal and 237 fecal samples were then screened for the presence of PEDV using DAS-qELISA and reverse transcriptase PCR (RT-PCR). DAS-qELISA had a high specificity of 98.1% and sensitivity of 93.5%. The accuracy rate between DAS-qELISA and RT-PCR was 95.7%. More importantly, the viral antigen concentrations remained unchanged before and after one inactivated vaccine preparation by using the DAS-qELISA. These results suggest DAS-qELISA could be used for antigen detection of inactivated vaccine samples and clinical samples. It is a novel method for diagnosing diseases and evaluation of the PEDV vaccine.

摘要

猪流行性腹泻病毒(PEDV)可导致哺乳仔猪急性腹泻和脱水,死亡率很高。在此,我们利用一种针对PEDV N蛋白的特异性单克隆抗体和抗PEDV兔血清,开发了一种用于检测PEDV的双抗体夹心定量酶联免疫吸附测定法(DAS-qELISA)。使用DAS-qELISA,重组PEDV N蛋白的检测限和病毒滴度分别约为1μg/L和10 TCID/ml。然后,使用DAS-qELISA和逆转录聚合酶链反应(RT-PCR)对总共90份肠道样本和237份粪便样本进行PEDV检测。DAS-qELISA具有98.1%的高特异性和93.5%的灵敏度。DAS-qELISA与RT-PCR之间的准确率为95.7%。更重要的是,通过使用DAS-qELISA,在制备一种灭活疫苗前后,病毒抗原浓度保持不变。这些结果表明,DAS-qELISA可用于灭活疫苗样本和临床样本的抗原检测。它是一种诊断疾病和评估PEDV疫苗的新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/645d/7649156/cfe980b1a762/fvets-07-540248-g0001.jpg

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