Robust BICP0-gB indirect ELISA for the accurate diagnosis of bovine alphaherpesvirus 1 infections

IF 1.9 Q2 AGRICULTURE, DAIRY & ANIMAL SCIENCE
Sen Zhang , Liyuan Song , Xin Yin , Changmin Hu , Yingyu Chen , Aizhen Guo
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Abstract

Bovine alphaherpesvirus 1 (BoHV-1) represents a significant threat to the cattle industry, emphasizing the need for reliable diagnostic tools that facilitate effective disease management. Current diagnostic methods, including virus neutralization tests (VNTs), are often complex and labor intensive, but existing antibody detection assays may lack sufficient accuracy. In this study, we developed a novel indirect enzyme-linked immunosorbent assay (iELISA) utilizing both BICP0 and gB proteins to enhance the detection of BoHV-1 infections. The inclusion of BICP0, a pivotal protein during the early stages of viral infection, markedly improved the assay's specificity and sensitivity. The BICP0-gB iELISA exhibited a high degree of concordance with the VNT, demonstrating superior sensitivity and specificity. Preliminary clinical evaluations revealed a real prevalence of 40.3 % (95 % CI: 33.1 %-48.0 %) in serum samples from yaks in Qinghai Province, which aligns with the documented prevalence of BoHV-1 in the region. These results underscore that BICP0-gB iELISA is a robust and reliable diagnostic tool for the differential diagnosis of BoHV-1, providing a cost-effective and efficient solution for high-throughput screening in the livestock industry.
准确诊断牛甲疱疹病毒1型感染的强有力的BICP0-gB间接ELISA方法
牛甲疱疹病毒1型(BoHV-1)对养牛业构成重大威胁,强调需要可靠的诊断工具,促进有效的疾病管理。目前的诊断方法,包括病毒中和试验(vnt),通常是复杂和劳动密集型的,但现有的抗体检测分析可能缺乏足够的准确性。在这项研究中,我们开发了一种新的间接酶联免疫吸附试验(iELISA),利用BICP0和gB蛋白来增强BoHV-1感染的检测。BICP0是病毒感染早期的一种关键蛋白,它的加入显著提高了检测的特异性和敏感性。BICP0-gB iELISA与VNT高度一致,具有较高的敏感性和特异性。初步临床评估显示,青海省牦牛血清样本的实际流行率为40.3% (95% CI: 33.1% - 48.0%),这与该地区记录的BoHV-1流行率一致。这些结果表明,BICP0-gB iELISA是一种稳健可靠的BoHV-1鉴别诊断工具,为畜牧业高通量筛查提供了一种经济高效的解决方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Veterinary and Animal Science
Veterinary and Animal Science Veterinary-Veterinary (all)
CiteScore
3.50
自引率
0.00%
发文量
43
审稿时长
47 days
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