Department of Medical Microbiology and Infectious Diseases, Erasmus University Medical Center, Rotterdam, The Netherlands; Department of Viroscience, Erasmus University Medical Center, Rotterdam, The Netherlands.
Department of Viroscience, Erasmus University Medical Center, Rotterdam, The Netherlands.
J Clin Virol. 2017 Jul;92:25-31. doi: 10.1016/j.jcv.2017.05.001. Epub 2017 May 3.
Diagnostic requests for both Zika virus (ZIKV) and dengue virus (DENV) infections in returning travelers have significantly increased during the recent ZIKV outbreak in the Americás. These flaviviruses have overlapping clinical syndromes and geographical distribution, but diagnostic differentiation is important because of different clinical consequences. As flaviviruses are known to have a short viremic period, diagnostics often rely on serological methods, which are challenging due to extensive cross-reactive antibodies.
To re-evaluate the performance of DENV serological assays in laboratory confirmed ZIKV-infected travelers.
The extent of cross-reactivity of the DENV NS1 antigen, IgM and IgG ELISA was analyzed in 152 clinical blood samples collected from 69 qRT-PCR and 24 virus neutralization titer (VNT) confirmed ZIKV-infected travelers.
The majority of travelers in the presented cohort returned to the Netherlands from Suriname and presented with symptoms of fever and rash. Twenty-three percent of the female travelers were pregnant. None of the 39 ZIKV RNA positive blood samples were cross-reactive in the DENV NS1 antigen ELISA. The rates of cross-reactivity of the DENV IgM and IgG ELISÁs were 31% and 54%, respectively, after excluding travelers with (potential) previous DENV exposure.
Although the DENV NS1 antigen assay was highly specific in this cohort of laboratory confirmed ZIKV-infected travelers, we demonstrate high percentages of cross-reactivity of DENV IgM and IgG ELISÁs of which diagnostic laboratories should be aware. In addition, the high rate of DENV IgG background of >25% complicates a proper serological diagnosis in this group.
在美洲最近的寨卡病毒(ZIKV)爆发期间,返回旅行者对寨卡病毒和登革热病毒(DENV)感染的诊断请求显著增加。这些黄病毒具有重叠的临床综合征和地理分布,但由于临床后果不同,诊断区分很重要。由于黄病毒的病毒血症期很短,因此诊断通常依赖于血清学方法,但由于广泛的交叉反应性抗体,这些方法具有挑战性。
重新评估实验室确认的寨卡病毒感染旅行者中 DENV 血清学检测的性能。
分析了从 69 名 qRT-PCR 和 24 名病毒中和滴度(VNT)确诊的寨卡病毒感染旅行者采集的 152 份临床血液样本中 DENV NS1 抗原、IgM 和 IgG ELISA 的交叉反应程度。
本研究队列中的大多数旅行者从苏里南返回荷兰,并出现发热和皮疹症状。23%的女性旅行者怀孕。在排除具有(潜在)先前 DENV 暴露的旅行者后,39 份 ZIKV RNA 阳性血样均未在 DENV NS1 抗原 ELISA 中出现交叉反应。DENV IgM 和 IgG ELISA 的交叉反应率分别为 31%和 54%。
尽管在本实验室确认的寨卡病毒感染旅行者队列中,DENV NS1 抗原检测具有很高的特异性,但我们证明 DENV IgM 和 IgG ELISA 的交叉反应率很高,诊断实验室应注意这一点。此外,DENV IgG 背景率>25%的高比例使该组的适当血清学诊断复杂化。