Loyola Steev, Huaman Alfredo, Popuche Dina, Castillo Elizabeth, Ampuero Julia S, Silva Maria, Guevara Carolina, Watts Douglas M
U.S. Naval Medical Research Unit No. 6 (NAMRU-6), Lima 07006, Peru.
Vysnova Partners Inc., Landover, Hyattsville, MD 20785, USA.
Diagnostics (Basel). 2021 Sep 17;11(9):1696. doi: 10.3390/diagnostics11091696.
Zika virus (ZIKV) emerged and spread rapidly in South American countries during 2015. Efforts to diagnose ZIKV infection using serological tools were challenging in dengue-endemic areas because of antigenic similarities between both viruses. Here, we assessed the performance of an in-house developed IgM antibody capture enzyme-linked immunosorbent assay (MAC-ELISA) and the plaque reduction neutralization test (PRNT) to diagnose ZIKV infection. Acute and convalescent paired serum samples from 51 patients who presented with clinical symptoms suggestive of an arbovirus illness in dengue-endemic areas of Honduras, Venezuela, Colombia and Peru were used in the assessment. Samples were tested for ZIKV, dengue and chikungunya virus using a variety of laboratory techniques. The results for the ZIKV-RNA screening and seroconversion detected by the microneutralization test were used to construct a composite reference standard. The overall sensitivity and specificity for the MAC-ELISA were 93.5% and 100.0%, respectively. Contrastingly, the overall sensitivity and specificity for the PRNT were 96.8% and 95.0%, respectively. Restricting the analysis according to IgM or neutralizing antibodies against dengue, the performances of both serological assays were adequate. The findings of this study reveal that the MAC-ELISA and PRNT would provide initial reliable laboratory diagnostic assays for ZIKV infection in dengue-endemic areas.
2015年期间,寨卡病毒(ZIKV)在南美国家出现并迅速传播。由于两种病毒之间存在抗原相似性,在登革热流行地区,使用血清学工具诊断ZIKV感染颇具挑战。在此,我们评估了一种自行开发的IgM抗体捕获酶联免疫吸附测定法(MAC-ELISA)和蚀斑减少中和试验(PRNT)诊断ZIKV感染的性能。评估中使用了来自洪都拉斯、委内瑞拉、哥伦比亚和秘鲁登革热流行地区51例出现虫媒病毒病临床症状患者的急性期和恢复期配对血清样本。使用多种实验室技术对样本进行ZIKV、登革热和基孔肯雅病毒检测。通过微量中和试验检测到的ZIKV-RNA筛查和血清转化结果用于构建综合参考标准。MAC-ELISA的总体敏感性和特异性分别为93.5%和100.0%。相比之下,PRNT的总体敏感性和特异性分别为96.8%和95.0%。根据针对登革热的IgM或中和抗体进行分析,两种血清学检测方法的性能均足够。本研究结果表明,MAC-ELISA和PRNT可为登革热流行地区的ZIKV感染提供初步可靠的实验室诊断检测方法。