Autor(es): Wahed, Ahmed Abd El ; Sanabani, Sabri S. ; Faye, Oumar ; Pessoa, Rodrigo ; Patriota, Joao-Veras ; Rodrigues-Giorgi, Rodrigues ; Patel, Pranav ; Boehlken-Fascher, Susanne ; Landt, Olfert ; Niedrig, Matthias ; Zanotto, Paolo M. de A. ; Czerny, Claus-Peter ; Sall, Amadou A. ; Weidmann, Manfred

Resumo: Currently detection of Zika virus (ZIKV) in patient samples is done by real-time RT-PCR. Samples collected from rural area are sent to highly equipped laboratories for screening. A rapid point-of-care test is needed to detect the virus, especially at low resource settings. Methodology/Principal Findings: In this report, we describe the development of a reverse transcription isothermal recombinase polymerase amplification (RT-RPA) assay for the identification of ZIKV. RT-RPA assay was portable, sensitive (21 RNA molecules), and rapid (3-15 minutes). No cross-reactivity was detected to other flaviviruses, alphaviruses and arboviruses. Compared to real-time RT-PCR, the diagnostic sensitivity was 92% while the specificity was 100%. Conclusions/Significance: The developed assay is a promising platform for rapid point of need detection of ZIKV in low resource settings and elsewhere (e.g. during mass gathering)

Imprenta: BiorXiv Beta, 2016

Identificador do objeto digital: 10.1101/078501

Descritores: ZIKV - Viral infections ; ZIKV - RT-PCR ; ZIKV - PCR detection

Data de publicação: 2016