Rapid detection of type A influenza viruses with monoclonal antibodies to the M protein (M1) by enzyme-linked immunosorbent assay and time-resolved fluoroimmunoassay

Author:

Bucher D J1,Mikhail A1,Popple S1,Graves P1,Meiklejohn G1,Hodes D S1,Johansson K1,Halonen P E1

Affiliation:

1. Department of Microbiology and Immunology, New York Medical College, Valhalla 10595.

Abstract

Monoclonal antibodies (MAbs) to the M protein (M1) were used in the development of direct detection systems for type A influenza viruses in clinical specimens. Optimal detection by an enzyme-linked immunosorbent assay was achieved when MAbs were used as capture antibodies and rabbit polyclonal antibodies were used as sandwich antibodies. Detection by the enzyme-linked immunosorbent assay required amplification of the virus. direct detection in clinical specimens (nasopharyngeal aspirates) was accomplished when MAbs recognizing two distinct antigenic sites of M1 were used in a time-resolved fluoroimmunoassay. Type A influenza viruses could be detected equally well in specimens obtained during epidemics of both H3N2 and H1N1 influenza viruses.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

Reference9 articles.

1. M-protein (Ml) of influenza virus: antigenic analysis and intracellular localization with monoclonal antibodies;Bucher D.;J. Virol.,1989

2. Detection of influenza viruses through selective adsorption and detection of the M-protein antigen;Bucher D. J.;J. Immunol. Methods,1987

3. Detection of viral antigens by time-resolved fluoroimmunoassay;Halonen P.;Curr. Top. Microbiol. Immunol.,1983

4. Europium as a label in time-resolved immunofluorometric assays;Hemmila I. S.;Anal. Biochem.,1984

5. The sequence of the nucleoprotein gene of human influenza A virus, strain A/NT/60-68;Huddleston I. A.;Nucleic Acids Res.,1982

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