Rodriguez Ana, Alonso-Morales Rogelio A, Lassala Arantzatzu, Rangel P Lucia, Ramírez-Andoney Vianey, Gutierrez Carlos G
Facultad de Medicina Veterinaria y Zootecnia, Universidad Nacional Autónoma de México, Cd. México, Mexico.
Access Microbiol. 2023 Oct 17;5(10). doi: 10.1099/acmi.0.000511.v3. eCollection 2023.
Animal welfare and economic implications of infectious diseases in cattle demand an efficient surveillance as the foundation for control and eradication programmes. Bovine respiratory syncytial virus (BRSV), Parainfluenza virus type 3 (PI3V), Bovine herpes virus-1 (BoHV-1), Bovine viral diarrhoea virus (BVDV), and Enzootic bovine leukosis virus (EBLV) cause common and often underdiagnosed diseases in cattle that are endemic in most countries [1]. A hallmark of individual exposure to a viral pathogen is the presence of antibodies directed towards that virus. The aim of this study was to develop and validate a pentaplex assay to simultaneously detect and quantify antibodies against BRSV, PI3V, BoHV-1, BVDV and EBLV in serum, as an efficient tool to yield epidemiological data. Monoplex assays were initially developed using either complete BRSV or BoHV-1 viral lysates, or recombinant proteins for BVDV, EBLV or PI3V as capture antigens. In addition, 125 serum samples from unvaccinated cattle, which were classified as positive or negative for each of the viruses by commercial ELISA kits, were used for validation. Conditions established for the Luminex monoplex assays were adopted for the pentaplex assay. The accuracy, determined by the area under the ROC curve, was greater than 0.97, and assay diagnostic sensitivities and specificities were over 95 and 90%, respectively, for all antigens. Intra (r) and interassay (R) coefficients of variation were under 10 and 20 %, respectively. Selectivity towards target viruses was shown by binding inhibition assays where unbound viruses reduced fluorescence intensities. Diagnostic agreement for samples analysed simultaneously in the monoplex and multiplex assays was almost perfect. In conclusion, a highly sensitive pentaplex assay was validated for the simultaneous identification of antibodies directed against BVDV, BoHV-1, PI3V, BRSV and EBLV in serum. The developed pentaplex assay complies with performance characteristics established by international guidelines for diagnostic tests and may be used as a tool for the implementation of epidemiological surveillance.
牛传染病对动物福利和经济的影响要求进行高效监测,作为控制和根除计划的基础。牛呼吸道合胞病毒(BRSV)、3型副流感病毒(PI3V)、牛疱疹病毒1型(BoHV-1)、牛病毒性腹泻病毒(BVDV)和地方流行性牛白血病病毒(EBLV)在大多数国家流行,会引发牛常见且常未被诊断出的疾病[1]。个体接触病毒病原体的一个标志是存在针对该病毒的抗体。本研究的目的是开发并验证一种五重检测法,用于同时检测和定量血清中针对BRSV、PI3V、BoHV-1、BVDV和EBLV的抗体,作为获取流行病学数据的有效工具。单重检测法最初使用完整的BRSV或BoHV-1病毒裂解物,或用于BVDV、EBLV或PI3V的重组蛋白作为捕获抗原进行开发。此外,125份来自未接种疫苗牛的血清样本,通过商业ELISA试剂盒对每种病毒分类为阳性或阴性,用于验证。五重检测法采用了为Luminex单重检测法建立的条件。通过ROC曲线下面积确定的准确性大于0.97,所有抗原的检测诊断敏感性和特异性分别超过95%和90%。批内(r)和批间(R)变异系数分别低于10%和20%。结合抑制试验显示了对目标病毒的选择性,未结合的病毒降低了荧光强度。单重和多重检测法同时分析的样本的诊断一致性几乎完美。总之,一种高度灵敏的五重检测法经验证可用于同时鉴定血清中针对BVDV、BoHV-1、PI3V、BRSV和EBLV的抗体。所开发的五重检测法符合国际诊断试验指南确立的性能特征,可作为实施流行病学监测的工具。