Highly sensitive detection of influenza virus by boron-doped diamond electrode terminated with sialic acid-mimic peptide

The progression of influenza varies according to age and the presence of an underlying disease; appropriate treatment is therefore required to prevent severe disease. Anti-influenza therapy, such as with neuraminidase inhibitors, is effective, but diagnosis at an early phase of infection before vira...

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Published inProceedings of the National Academy of Sciences - PNAS Vol. 113; no. 32; pp. 8981 - 8984
Main Authors Matsubara, Teruhiko, Ujie, Michiko, Yamamoto, Takashi, Akahori, Miku, Einaga, Yasuaki, Sato, Toshinori
Format Journal Article
LanguageEnglish
Published United States National Academy of Sciences 09.08.2016
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Summary:The progression of influenza varies according to age and the presence of an underlying disease; appropriate treatment is therefore required to prevent severe disease. Anti-influenza therapy, such as with neuraminidase inhibitors, is effective, but diagnosis at an early phase of infection before viral propagation is critical. Here, we show that several dozen plaque-forming units (pfu) of influenza virus (IFV) can be detected using a boron-doped diamond (BDD) electrode terminated with a sialic acid-mimic peptide. The peptide was used instead of the sialyloligosaccharide receptor, which is the common receptor of influenza A and B viruses required during the early phase of infection, to capture IFV particles. The peptide, which was previously identified by phage-display technology, was immobilized by click chemistry on the BDD electrode, which has excellent electrochemical characteristics such as low background current and weak adsorption of biomolecules. Electrochemical impedance spectroscopy revealed that H1N1 and H3N2 IFVs were detectable in the range of 20–500 pfu by using the peptide-terminated BDD electrode. Our results demonstrate that the BDD device integrated with the receptor-mimic peptide has high sensitivity for detection of a low number of virus particles in the early phase of infection.
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Edited by Thomas E. Mallouk, The Pennsylvania State University, University Park, PA, and approved June 17, 2016 (received for review March 3, 2016)
Author contributions: T.M. and T.S. designed research; T.M. and M.U. performed research; T.Y., M.A., and Y.E. contributed new reagents/analytic tools; T.M., M.U., T.Y., and Y.E. analyzed data; and T.M. and T.S. wrote the paper.
ISSN:0027-8424
1091-6490
1091-6490
DOI:10.1073/pnas.1603609113