Testing of diagnostic test-systems for detection of antibodies to foot-and-mouth disease virus structural proteins with enzyme-linked immunosorbent assay for their serotype specificity

N. N. Lugovskaya, E. A. Silanteva, T. V. Okovytaya, A. A. Kharitonova, Y. M. Gochmuradov, E. A. Razgulyaeva, O. O. Budina, E. A. Yasneva
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Abstract

A total of 138 serum samples from pigs and cattle vaccinated against foot-and-mouth disease virus (FMDV) of one or two serotypes or infected with FMDV were used for testing of 24 enzyme-linked immunosorbent assay (ELISA) diagnostic tests-systems for detection of antibodies against FMDV structural proteins produced by 6 manufacturers (Federal Centre for Animal Health, Prionics, IZSLER, Innovative Diagnostics, BIONOTE and MEDIAN Diagnostics) for their serotype-specificity. All used test-systems detected apparent serotype-specific activity (homologous reaction) as well as cross-reacting virus-specific antibodies that was accounted for some reasons related to conservative epitopes in amino acid sequence of FMDV virion capsid VP1–VP3 polypeptides, accessibility of internal conservative epitopes of VP4 polypeptide for the animal’s immune system during virus replication or vaccine antigen (virus) destruction in the animal’s body in the process of immunity development, as well as the pilot anti-FMD vaccine composition, etc. Nevertheless, the analysis of a large data set (about 3,500 tests) showed that the homologous serotype-specific reaction in general was significantly higher and predominant, the proportion of virus-specific non-protective antibodies, including cross-reacting ones, was not significant and did not distort the results of ELISA tests of anti-FMD vaccine for its immunogenicity. Inconclusive test results require confirmation with other serological tests. Complex tests for FMDV using different diagnostic methods such as ELISA with standard and reference test-systems and/or virus neutralization test in cell culture are to be considered as the best option.
用酶联免疫吸附测定法检测口蹄疫病毒结构蛋白抗体的诊断测试系统的血清型特异性
共采集了 138 份猪和牛的血清样本,这些样本分别接种了一种或两种血清型的口蹄疫病毒(FMDV)疫苗,或感染了口蹄疫病毒,用于检测 6 家制造商(联邦动物卫生中心、Prionics、IZSLER、创新诊断公司、BIONOTE 和 MEDIAN 诊断公司)生产的 24 种酶联免疫吸附试验(ELISA)诊断试验系统的血清型特异性,以检测针对口蹄疫病毒结构蛋白的抗体。所有使用的检测系统都能检测到明显的血清型特异性活性(同源反应)以及交叉反应的病毒特异性抗体,其原因与 FMDV 病毒荚膜 VP1-VP3 多肽氨基酸序列中的保守表位、病毒复制过程中 VP4 多肽内部保守表位对动物免疫系统的可及性、免疫发展过程中疫苗抗原(病毒)在动物体内的破坏以及试验性抗 FMD 疫苗的成分等有关。尽管如此,对大量数据集(约 3 500 次测试)的分析表明,同源血清型特异性反应一般明显较高且占主导地位,病毒特异性非保护性抗体(包括交叉反应抗体)的比例并不显著,不会扭曲抗口蹄疫疫苗免疫原性的 ELISA 测试结果。不确定的检测结果需要通过其他血清学检测来确认。最佳选择是使用不同的诊断方法对口蹄疫病毒进行复合检测,如使用标准和参考检测系统进行 ELISA 检测和/或在细胞培养中进行病毒中和检测。
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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