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DOI 10.1016/j.jviromet.2017.02.011

Медицинская библиотека · Journal of virological methods · 2017

Utility of Japanese encephalitis virus subgenomic replicon-based single-round infectious particles as antigens in neutralization tests for Zika virus and three other flaviviruses.

Yamanaka Atsushi, Moi Meng Ling, Takasaki Tomohiko, Kurane Ichiro, Matsuda Mami, Suzuki Ryosuke, Konishi Eiji

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

The introduction of a foreign virus into an area may cause an outbreak, as with the Zika virus (ZIKV) outbreak in the Americas. Preparedness for handling a viral outbreak involves the development of tests for the serodiagnosis of foreign virus infections. We previously established a gene-based technology to generate some flaviviral antigens useful for functional antibody assays. The technology utilizes a Japanese encephalitis virus subgenomic replicon to generate single-round infectious particles (SRIPs) that possess designed surface antigens. In the present study, we successfully expanded the capacity of SRIPs to four human-pathogenic mosquito-borne flaviviruses that could potentially be introduced from endemic to non-endemic countries: ZIKV, Sepik virus, Wesselsbron virus, and Usutu virus. Flavivirus-crossreactive monoclonal antibodies dose-dependently neutralized these SRIPs. ZIKV-SRIPs also produced antibody-dose-dependent neutralization curves equivalent to those shown by authentic ZIKV particles using sera from a Zika fever patient. The faithful expression of designed surface antigens on SRIPs will allow their use in neutralization tests to diagnose foreign flaviviral infections.

Для цитирования: Yamanaka Atsushi, Moi Meng Ling, Takasaki Tomohiko, Kurane Ichiro, Matsuda Mami, Suzuki Ryosuke, Konishi Eiji. Utility of Japanese encephalitis virus subgenomic replicon-based single-round infectious particles as antigens in neutralization tests for Zika virus and three other flaviviruses.. Journal of virological methods. 2017. DOI: 10.1016/j.jviromet.2017.02.011.

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