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鉴定非洲猪瘟病毒 p54 蛋白中的保守位点及其在血清学检测中的初步应用。

Identification of a conservative site in the African swine fever virus p54 protein and its preliminary application in a serological assay.

机构信息

National and Regional Joint Engineering Laboratory for Medicament of Zoonoses Prevention and Control, College of Veterinary Medicine, South China Agricultural University, Guangzhou 510642, China.

Shenzhen Customs District P.R. China, Shenzhen 518045, China.

出版信息

J Vet Sci. 2022 Jul;23(4):e55. doi: 10.4142/jvs.21134. Epub 2022 May 16.

Abstract

BACKGROUND

ASF was first reported in Kenya in 1910 in 1921. In China, ASF spread to 31 provinces including Henan and Jiangsu within six months after it was first reported on August 3, 2018. The epidemic almost affected the whole China, causing direct economic losses of tens of billions of yuan. Cause great loss to our pig industry. As ELISA is cheap and easy to operate, OIE regards it as the preferred serological method for ASF detection. P54 protein has good antigenicity and is an ideal antigen for detection.

OBJECTIVE

To identify a conservative site in the African swine fever virus (ASFV) p54 protein and perform a Cloth-enzyme-linked immunosorbent assay (ELISA) for detecting the ASFV antibody in order to reduce risks posed by using the live virus in diagnostic assays.

METHOD

We used bioinformatics methods to predict the antigen epitope of the ASFV p54 protein in combination with the antigenic index and artificially synthesized the predicted antigen epitope peptides. Using ASFV-positive serum and specific monoclonal antibodies (mAbs), we performed indirect ELISA and blocking ELISA to verify the immunological properties of the predicted epitope polypeptide.

RESULTS

The results of our prediction revealed that the possible antigen epitope regions were A23-29, A36-45, A72-94, A114-120, A124-130, and A137-150. The indirect ELISA showed that the peptides A23-29, A36-45, A72-94, A114-120, and A137-150 have good antigenicity. Moreover, the A36-45 polypeptide can react specifically with the mAb secreted by hybridoma cells, and its binding site contains a minimum number of essential amino acids in the sequence 37DIQFINPY44.

CONCLUSIONS

Our study confirmed a conservative antigenic site in the ASFV p54 protein and its amino acid sequence. A competitive ELISA method for detecting ASFV antibodies was established based on recombinant p54 and matching mAb. Moreover, testing the protein sequence alignment verified that the method can theoretically detect antibodies produced by pigs affected by nearly all ASFVs worldwide.

摘要

背景

1910 年 ASF 首次在肯尼亚报告,1921 年在中国报告。自 2018 年 8 月 3 日首次报告以来,ASF 在六个月内传播到包括河南和江苏在内的中国 31 个省。疫情几乎波及全国,造成数十亿元的直接经济损失。对我国养猪业造成了巨大损失。由于 ELISA 价格便宜且易于操作,OIE 将其视为 ASF 检测的首选血清学方法。P54 蛋白具有良好的抗原性,是检测的理想抗原。

目的

鉴定非洲猪瘟病毒(ASFV)p54 蛋白中的保守位点,并进行酶联免疫吸附试验(ELISA)检测 ASFV 抗体,以降低使用活病毒进行诊断检测的风险。

方法

我们使用生物信息学方法预测 ASFV p54 蛋白的抗原表位,结合抗原指数和人工合成预测的抗原表位肽。使用 ASFV 阳性血清和特异性单克隆抗体(mAb)进行间接 ELISA 和阻断 ELISA,以验证预测的表位多肽的免疫特性。

结果

预测结果表明,可能的抗原表位区域为 A23-29、A36-45、A72-94、A114-120、A124-130 和 A137-150。间接 ELISA 表明,肽 A23-29、A36-45、A72-94、A114-120 和 A137-150 具有良好的抗原性。此外,A36-45 多肽可与杂交瘤细胞分泌的 mAb 特异性反应,其结合部位在序列 37DIQFINPY44 中包含最少数量的必需氨基酸。

结论

本研究证实了 ASFV p54 蛋白及其氨基酸序列中的一个保守抗原位点。基于重组 p54 和匹配的 mAb 建立了检测 ASFV 抗体的竞争性 ELISA 方法。此外,通过对蛋白序列比对的检测验证了该方法理论上可以检测到由全球几乎所有 ASFVs 感染的猪产生的抗体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdc6/9346533/420504fe1c5e/jvs-23-e55-g001.jpg

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