Steinhagen Katja, Probst Christian, Radzimski Christiane, Schmidt-Chanasit Jonas, Emmerich Petra, van Esbroeck Marjan, Schinkel Janke, Grobusch Martin P, Goorhuis Abraham, Warnecke Jens M, Lattwein Erik, Komorowski Lars, Deerberg Andrea, Saschenbrecker Sandra, Stöcker Winfried, Schlumberger Wolfgang
Institute for Experimental Immunology, EUROIMMUN AG, Lübeck, Germany.
WHO Collaborating Centre for Arbovirus and Haemorrhagic Fever Reference and Research, Bernhard-Nocht Institute for Tropical Medicine, Hamburg, Germany.
Euro Surveill. 2016 Dec 15;21(50). doi: 10.2807/1560-7917.ES.2016.21.50.30426.
Serological diagnosis of Zika virus (ZIKV) infections is challenging due to high cross-reactivity between flaviviruses. We evaluated the diagnostic performance of a novel anti-ZIKV ELISA based on recombinant ZIKV non-structural protein 1 (NS1). Assay sensitivity was examined using sera from 27 patients with reverse transcription (RT)-PCR-confirmed and 85 with suspected ZIKV infection. Specificity was analysed using sera from 1,015 healthy individuals. Samples from 252 patients with dengue virus (n = 93), West Nile virus (n = 34), Japanese encephalitis virus (n = 25), chikungunya virus (n = 19) or Plasmodium spp. (n = 69) infections and from 12 yellow fever-vaccinated individuals were also examined. In confirmed ZIKV specimens collected ≥ 6 days after symptom onset, ELISA sensitivity was 58.8% (95% confidence interval (CI): 36.0-78.4) for IgM, 88.2% (95% CI: 64.4-98.0) for IgG, and 100% (95% CI: 78.4-100) for IgM/IgG, at 99.8% (95% CI: 99.2-100) specificity. Cross-reactivity with high-level dengue virus antibodies was not detected. Among patients with potentially cross-reactive antibodies anti-ZIKV positive rates were 0.8% (95% CI: 0-3.0) and 0.4% (95% CI: 0-2.4) for IgM and IgG, respectively. Providing high specificity and low cross-reactivity, the NS1-based ELISA has the potential to aid in counselling patients, pregnant women and travellers after returning from ZIKV-endemic areas.
由于黄病毒之间存在高度交叉反应性,寨卡病毒(ZIKV)感染的血清学诊断具有挑战性。我们评估了一种基于重组ZIKV非结构蛋白1(NS1)的新型抗ZIKV ELISA的诊断性能。使用来自27例经逆转录(RT)-PCR确诊的患者和85例疑似ZIKV感染患者的血清检测了该检测方法的敏感性。使用来自1015名健康个体的血清分析了特异性。还检测了来自252例登革热病毒(n = 93)、西尼罗河病毒(n = 34)、日本脑炎病毒(n = 25)、基孔肯雅病毒(n = 19)或疟原虫属(n = 69)感染患者以及12名接种黄热病疫苗个体的样本。在症状出现后≥6天采集的确诊ZIKV标本中,ELISA检测IgM的敏感性为58.8%(95%置信区间(CI):36.0 - 78.4),IgG为88.2%(95%CI:64.4 - 98.0),IgM/IgG为100%(95%CI:78.4 - 100),特异性为99.8%(95%CI:99.2 - 100)。未检测到与高水平登革热病毒抗体的交叉反应。在具有潜在交叉反应性抗体的患者中,IgM和IgG的抗ZIKV阳性率分别为0.8%(95%CI:0 - 3.0)和0.4%(95%CI:0 - 2.4)。基于NS1的ELISA具有高特异性和低交叉反应性,有可能帮助为来自ZIKV流行地区的患者、孕妇和旅行者提供咨询。