Detection of influenza viruses through selective adsorption and detection of the M-protein antigen
Identifieur interne : 001344 ( Istex/Curation ); précédent : 001343; suivant : 001345Detection of influenza viruses through selective adsorption and detection of the M-protein antigen
Auteurs : Doris J. Bucher [États-Unis] ; Igor G. Kharitonenkov [Russie] ; M. Wajeed Khan [États-Unis] ; Arlette Palo [Russie] ; Denise Holloway [Russie] ; Adel Mikhail [Russie]Source :
- Journal of Immunological Methods [ 0022-1759 ] ; 1987.
English descriptors
- Teeft :
- Absorbance, Academic press, Adsorption, Adsorption time, Alkaline phosphatase, Allantoic fluid, Assay, Bead, Bovine, Bovine serum albumin, Bucher, Carbonate, Carbonate buffer, Carbonate coating buffer, Crossreactive epitope, Diethanolamine buffer, Elisa, Elisa assay, Higher levels, Hydrophobic properties, Hyperimmune, Hyperimmune antiserum, Hyperimmune sera, Influenza, Influenza virus, Influenza virus preparations, Influenza viruses, Kilbourne, Levy place, Lipid bilayer, Methods section, Microtiter plates, Model system, Optimized protocol, Parainfluenza virus type, Parent strain, Phosphate substrate, Polystyrene, Polystyrene bead, Polystyrene beads, Polystyrene surface, Practical virology, Rabbit serum, Recombinant strain, Research methods, Rhabdovirus group, Room temperature, Sarkosyl, Selective adsorption, Selective adsorption technique, Sendai, Sendai virus, Serum albumin, Sigma chemical, Sinai school, Swine influenza, Test system, Throat wash specimens, Veal infusion broth, Veterinary diseases, Viral, Viral agents, Viral particles, Virology, Virus, Virus preparations.
Abstract
Abstract: A model system has been developed which permits rapid detection of influenza viruses through targeting of the M (membrane or matrix)-protein; a type-specific antigen, in an enzyme-linked immunosorbent assay system. This technique exploits the hydrophobic properties of M-protein; the M-protein is selectively and rapidly adsorbed to polysterene surfaces even in the presence of a 5000-fold excess of bovine serum albumin. Hyperimmune antiserum prepared to purified M-protein is used as the detecting reagent. All type A influenza viruses could be detected by this technique, type B influenza viruses reacted to a slight extent and Sendai virus (parainfluenza virus, type 1) did not react. Virus could be detected to levels as low as 3 ng. Purification of M-protein and preparation of hyperimmune sera from other related virus groups, such as type B influenza viruses, paramyxoviruses and rhabdoviruses should permit detection of these agents by a similar technique.
Url:
DOI: 10.1016/0022-1759(87)90370-X
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<term>Academic press</term>
<term>Adsorption</term>
<term>Adsorption time</term>
<term>Alkaline phosphatase</term>
<term>Allantoic fluid</term>
<term>Assay</term>
<term>Bead</term>
<term>Bovine</term>
<term>Bovine serum albumin</term>
<term>Bucher</term>
<term>Carbonate</term>
<term>Carbonate buffer</term>
<term>Carbonate coating buffer</term>
<term>Crossreactive epitope</term>
<term>Diethanolamine buffer</term>
<term>Elisa</term>
<term>Elisa assay</term>
<term>Higher levels</term>
<term>Hydrophobic properties</term>
<term>Hyperimmune</term>
<term>Hyperimmune antiserum</term>
<term>Hyperimmune sera</term>
<term>Influenza</term>
<term>Influenza virus</term>
<term>Influenza virus preparations</term>
<term>Influenza viruses</term>
<term>Kilbourne</term>
<term>Levy place</term>
<term>Lipid bilayer</term>
<term>Methods section</term>
<term>Microtiter plates</term>
<term>Model system</term>
<term>Optimized protocol</term>
<term>Parainfluenza virus type</term>
<term>Parent strain</term>
<term>Phosphate substrate</term>
<term>Polystyrene</term>
<term>Polystyrene bead</term>
<term>Polystyrene beads</term>
<term>Polystyrene surface</term>
<term>Practical virology</term>
<term>Rabbit serum</term>
<term>Recombinant strain</term>
<term>Research methods</term>
<term>Rhabdovirus group</term>
<term>Room temperature</term>
<term>Sarkosyl</term>
<term>Selective adsorption</term>
<term>Selective adsorption technique</term>
<term>Sendai</term>
<term>Sendai virus</term>
<term>Serum albumin</term>
<term>Sigma chemical</term>
<term>Sinai school</term>
<term>Swine influenza</term>
<term>Test system</term>
<term>Throat wash specimens</term>
<term>Veal infusion broth</term>
<term>Veterinary diseases</term>
<term>Viral</term>
<term>Viral agents</term>
<term>Viral particles</term>
<term>Virology</term>
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<front><div type="abstract" xml:lang="en">Abstract: A model system has been developed which permits rapid detection of influenza viruses through targeting of the M (membrane or matrix)-protein; a type-specific antigen, in an enzyme-linked immunosorbent assay system. This technique exploits the hydrophobic properties of M-protein; the M-protein is selectively and rapidly adsorbed to polysterene surfaces even in the presence of a 5000-fold excess of bovine serum albumin. Hyperimmune antiserum prepared to purified M-protein is used as the detecting reagent. All type A influenza viruses could be detected by this technique, type B influenza viruses reacted to a slight extent and Sendai virus (parainfluenza virus, type 1) did not react. Virus could be detected to levels as low as 3 ng. Purification of M-protein and preparation of hyperimmune sera from other related virus groups, such as type B influenza viruses, paramyxoviruses and rhabdoviruses should permit detection of these agents by a similar technique.</div>
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