Antibody-free digital influenza virus counting based on neuraminidase activity
Autor: | Yoichiro Fujioka, Seiya Yamayoshi, Kazuhito V. Tabata, Yusuke Ohba, Yoshihiro Kawaoka, Yoshiki Moriizumi, Yoshihiro Minagawa, Yuko Kawaguchi, Hiroyuki Noji, Mana Ono |
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Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
Oseltamivir viruses Neuraminidase lcsh:Medicine medicine.disease_cause Virus Article 03 medical and health sciences chemistry.chemical_compound Viral Proteins 0302 clinical medicine Influenza A Virus H1N1 Subtype Influenza A virus medicine lcsh:Science Detection limit Multidisciplinary biology Chemistry Influenza A Virus H3N2 Subtype lcsh:R Virion Virology Titer 030104 developmental biology biology.protein Alkaline phosphatase lcsh:Q Antibody 030217 neurology & neurosurgery |
Zdroj: | Scientific Reports, Vol 9, Iss 1, Pp 1-13 (2019) Scientific Reports |
ISSN: | 2045-2322 |
Popis: | There is large demand for a quantitative method for rapid and ultra-sensitive detection of the influenza virus. Here, we established a digital influenza virus counting (DIViC) method that can detect a single virion without antibody. In the assay, a virion is stochastically entrapped inside a femtoliter reactor array device for the fluorogenic assay of neuraminidase, and incubated for minutes. By analyzing 600,000 reactors, the practical limit of detection reached the order of 103 (PFU)/mL, only 10-times less sensitive than RT-PCR and more than 1000-times sensitive than commercial rapid test kits (RIDTs). Interestingly, neuraminidase activity differed among virions. The coefficient of variance was 30–40%, evidently broader than that of alkaline phosphatase measured as a model enzyme for comparison, suggesting the heterogeneity in size and integrity among influenza virus particles. Sensitivity to oseltamivir also differed between virions. We also tested DIViC using clinical gargle samples that imposes less burden for sampling while with less virus titre. The comparison with RIDTs showed that DIViC was largely superior to RIDTs in the sensitivity with the clinical samples although a few false-positive signals were observed in some clinical samples that remains as a technical challenge. |
Databáze: | OpenAIRE |
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