| Literature DB >> 27462094 |
Reiko Yoshida1, Shino Muramatsu2, Hiroshi Akita2, Yuji Saito2, Miwa Kuwahara2, Daisuke Kato2, Katendi Changula3, Hiroko Miyamoto1, Masahiro Kajihara1, Rashid Manzoor1, Wakako Furuyama1, Andrea Marzi4, Heinz Feldmann4, Aaron Mweene3, Justin Masumu5, Jimmy Kapeteshi6, Jean-Jacques Muyembe-Tamfum6, Ayato Takada7.
Abstract
The latest outbreak of Ebola virus disease (EVD) in West Africa has highlighted the urgent need for the development of rapid and reliable diagnostic assays. We used monoclonal antibodies specific to the ebolavirus nucleoprotein to develop an immunochromatography (IC) assay (QuickNavi-Ebola) for rapid diagnosis of EVD. The IC assay was first evaluated with tissue culture supernatants of infected Vero E6 cells and found to be capable of detecting 103-104 focus-forming units/mL of ebolaviruses. Using serum samples from experimentally infected nonhuman primates, we confirmed that the assay could detect the viral antigen shortly after disease onset. It was also noted that multiple species of ebolaviruses could be detected by the IC assay. Owing to the simplicity of the assay procedure and absence of requirements for special equipment and training, QuickNavi-Ebola is expected to be a useful tool for rapid diagnosis of EVD.Entities:
Keywords: EVD; Ebola virus; diagnosis; ebolavirus; filovirus; immunochromatography assay; monoclonal antibody; nucleoprotein
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Year: 2016 PMID: 27462094 PMCID: PMC5050476 DOI: 10.1093/infdis/jiw252
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226