FIELD: medicine.
SUBSTANCE: method involves sampling of a primary cell culture, its infection at a constant dose with strains of different cytopathogenicity, incuybation of the infected material, and evaluation of a degree of cytopathogenicity of the agent. The primary cell culture is presented by a cell suspension of peritoneal exudate of laboratory animals. A degree of viral cytopathogenicity is evaluated by variations of cytochemical enzymatic activity for the enzymes 5'-nucleotidase, ATP-ase, succinate dehydrogenase and the content of nitrogen oxide (NO) metabolites of the infected cells, in dynamics, in - 0.5,1, 2, 3, 5 and 6 h by measuring optical density of a substrate solution for each enzyme. An average cell activation value (CAVav) is calculated by formula: CAV=CAV0.5+CAV1+CAV2+CAV3+CAV5+CAV6/N; wherein N is a number of time intervals. A cell response index (CRI) is calculated by formula: CRI=CAVav/ CAV intact cells 100. The average value is derived, and if the values CRIav is less than 100, a degree of viral pathogenicity is considered to be high, while the values CRIav more than 100 show a low degree of viral pathogenicity.
EFFECT: method provides higher efficiency, information value and reliability of evaluation of a degree of viral pathogenicity.
2 cl, 4 tbl, 2 ex
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MARKER FOR ESTIMATING ATTENUATION OF POLIOMYELITIS VIRUSES | 0 |
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SU1799598A1 |
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RU2460773C2 |
Authors
Dates
2012-11-10—Published
2011-03-30—Filed