NS1-based ELISA test efficiently detects dengue infections without cross-reactivity with Zika virus

登革热病毒 血清学 病毒学 寨卡病毒 登革热 抗体 抗原 交叉反应性 菌斑减少中和试验 生物 重组DNA 免疫球蛋白M 病毒 免疫球蛋白G 免疫学 交叉反应 基因 生物化学
作者
Samuel Santos Pereira,Robert Andreata‐Santos,Lennon Ramos Pereira,Camila Pereira Soares,Alvina Clara Félix,Patrícia de Mello Jungmann Cardoso de Andrade,Edison L. Durigon,Camila Malta Romano,Luís Carlos de Souza Ferreira
出处
期刊:International Journal of Infectious Diseases [Elsevier BV]
卷期号:112: 202-204 被引量:7
标识
DOI:10.1016/j.ijid.2021.09.009
摘要

The aim of this study was to achieve greater specificity of dengue virus (DENV) serological tests based on a recombinant antigen derived from non-structural protein 1 (ΔNS1) with regard to cross-reactive Zika virus (ZIKV) anti-NS1 antibody responses. This is of relevance in endemic regions for the serological discrimination of both DENV and ZIKV, such as Brazil and other tropical countries.The ΔNS1 proteins were obtained as recombinant antigens and were evaluated as solid-phase-bound antigens in the ELISA test to detect anti-NS1 IgG antibodies. The performance of the ∆NS1-based DENV IgG ELISA was assessed with both mouse and human serum samples previously exposed to DENV or ZIKV.The ∆NS1-based DENV IgG ELISA detected anti-DENV NS1 IgG without cross-reactivity with ZIKV-positive serum samples. The sensitivity and specificity of the assay determined using samples previously characterized by real-time PCR (qRT-PCR) or plaque reduction neutralization assay (PRNT) were 82% and 93%, respectively.The ∆NS1-based DENV IgG ELISA conferred enhanced diagnostic specificity for anti-DENV serological tests and may be particularly useful for serological analyses in endemic regions for both DENV and ZIKV transmission.

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