One-step RT-PCR for detection of Zika virus

被引:193
作者
Faye, Oumar [1 ,4 ]
Faye, Ousmane [1 ]
Dupressoir, Anne [1 ,2 ]
Weidmann, Manfred [3 ]
Ndiaye, Mady [4 ]
Sall, Amadou Alpha [1 ]
机构
[1] Inst Pasteur, Dakar, Senegal
[2] Inst Gustave Roussy, CNRS, UMR8122, Villejuif, France
[3] Univ Gottingen, Inst Virol, D-37075 Gottingen, Germany
[4] Univ Cheikh Anta Diop Dakar, Dakar, Senegal
关键词
Zika virus; detection; diagnosis; RT-PCR;
D O I
10.1016/j.jcv.2008.05.005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Zika virus (ZIKV) is an emerging mosquito-borne flavivirus circulating in Asia and Africa. Human infection induces an influenza-like syndrome that is associated with retro-orbital pain, oedema, lymphadenopathy, or diarrhea. Diagnosis of Zika fever requires virus isolation and serology, which are time consuming or cross-reactive. Objective: To develop a one-step RT-PCR assay to detect ZIKV in human serum. Study design: An assay targeting the envelope protein coding region was designed and evaluated for its specificity, detection limit, repeatability, and capacity to detect ZIKV isolates collected over a 40-year period from various African countries and hosts. Results: The assay's detection limit and repeatability were respectively 7.7 pfu/reaction and 100% in serum and L-15 medium; none of 19 other flaviviruses tested were detected. Conclusions: The assay is rapid, sensitive, and specific to detect ZIKV in cell culture or serum, but needs to be validated for diagnosis using clinical samples. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:96 / 101
页数:6
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