Istituto Zooprofilattico Sperimentale della Lombardia e dell'Emilia Romagna, Brescia, Italy.
Istituto Zooprofilattico Sperimentale della Lombardia e dell'Emilia Romagna, Parma, Italy.
Transbound Emerg Dis. 2019 Jan;66(1):268-276. doi: 10.1111/tbed.13012. Epub 2018 Sep 17.
Influenza D virus (IDV) was first reported in 2011 in swine in Oklahoma and consequently found in cattle, sheep, and goats across North America and Eurasia. Cattle have been proposed as the natural reservoir. In this study, we developed and validated a MAb-based competitive ELISA for the detection of antibodies against IDV. Thirty-one hybridomas specific to IDV were generated using Balb/C mice immunised with purified IDV/Swine/Italy/199724-3/2015. The specificity of MAbs was determined by comparing their reactivity with the homologous and other influenza A viruses along with additional bovine and swine viruses. A solid-phase competitive ELISA (IDV-cELISA) was set up using the partially purified antigen coated to the plate and incubation of two serum dilutions (1/10 and 1/20) followed by addition of a peroxidase-conjugated MAb as competitor, which had shown wide intratype cross-reactivity and positivity in HI. To evaluate the diagnostic performances of IDV-cELISA, we used 884 sera (414 negative and 470 positive) from different species. ROC analyses were performed to enable the selection of best cut-off value and estimation of diagnostic specificity and sensitivity. The agreement between IDV-cELISA and HI test was assessed by Cohen's kappa value (κ). The κ analysis showed an almost perfect agreement (κ = 0.93; 95%CI -0.899 to 0.961) between HI test and IDV-cELISA. ROC analysis showed that IDV-cELISA was accurate with an area under the curve (AUC) = 0.999, 95% CI 0.993-1.000). A cut-off value of 65% was selected with Se and Sp values of 99.35 (95% CI 98.1-99.9) and 98.75 (95% CI 97.1-99.6). These results proved excellent diagnostic performances of IDV-cELISA, which compared to HI presented major advantages, such as suitability for automation, low dependence on individual skills, spectrophotometric reading, and easy interpretation of the results. This assay can be exploited to detect anti-IDV antibodies in different animal species.
流感 D 病毒(IDV)于 2011 年在俄克拉荷马州的猪群中首次报道,随后在北美和欧亚大陆的牛、绵羊和山羊中发现。牛被认为是其自然宿主。在本研究中,我们开发并验证了一种基于单抗的竞争性 ELISA 用于检测针对 IDV 的抗体。使用免疫原性纯化的 IDV/Swine/Italy/199724-3/2015 的 Balb/C 小鼠免疫产生了 31 株针对 IDV 的杂交瘤。通过比较它们与同源和其他甲型流感病毒以及其他牛和猪病毒的反应性来确定 MAbs 的特异性。使用部分纯化的抗原包被平板建立固相竞争 ELISA(IDV-cELISA),并孵育两种血清稀释度(1/10 和 1/20),然后加入过氧化物酶标记的单抗作为竞争物,该竞争物显示出广泛的同型交叉反应性和 HI 阳性。为了评估 IDV-cELISA 的诊断性能,我们使用了来自不同物种的 884 份血清(414 份阴性和 470 份阳性)。进行 ROC 分析以选择最佳截断值并估计诊断特异性和敏感性。通过 Cohen 的 kappa 值(κ)评估 IDV-cELISA 和 HI 试验之间的一致性。κ分析显示 HI 试验和 IDV-cELISA 之间存在几乎完美的一致性(κ=0.93;95%CI -0.899 至 0.961)。ROC 分析表明 IDV-cELISA 具有准确性,曲线下面积(AUC)为 0.999,95%CI 为 0.993-1.000。选择 65%作为截断值,Se 和 Sp 值分别为 99.35(95%CI 98.1-99.9)和 98.75(95%CI 97.1-99.6)。这些结果证明了 IDV-cELISA 的出色诊断性能,与 HI 相比,它具有自动化、对个体技能依赖性低、分光光度读数和结果易于解释等主要优势。该测定可用于检测不同动物物种中的抗 IDV 抗体。