Cargando…

Development and verification of real-time PCR assay for identification of viral agents causing acute respiratory infections in human beings

A multiplex polymerase chain reaction (PCR) for identification of four viruses causing acute respiratory diseases in human beings was developed. The analytical sensitivity of developed RT-PCR for identification of adenovirus, respiratory-syncytial virus, flu viruses types A and B, and actual subtype...

Descripción completa

Detalles Bibliográficos
Autores principales: Sergeeva, E. I., Ternovoi, V. A., Demina, O. K., Demina, A. V., Korneev, D. V., Shikov, A. N., Beryllo, S. A., Agafonov, A. P., Sergeev, A. N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7088833/
https://www.ncbi.nlm.nih.gov/pubmed/32214648
http://dx.doi.org/10.3103/S0891416813040083
Descripción
Sumario:A multiplex polymerase chain reaction (PCR) for identification of four viruses causing acute respiratory diseases in human beings was developed. The analytical sensitivity of developed RT-PCR for identification of adenovirus, respiratory-syncytial virus, flu viruses types A and B, and actual subtypes of type A flu virus (seasonal and pandemic variants H1N1, seasonal H3N2, and viruses of bird flu that are pathogenic to human beings H5 and H7) was 1 × 10(3) genome equivalents per milliliter. Diagnostic sensitivity for flu virus type A and B, and also subtypes H1 (seasonal H1N1, pandemic variant of H1N1 of year 2009), H3, H5 was 1 × 10(3)–10(4) viral particles per milliliter. The method developed has high specificity and does not have positive signal in experiments with DNA/cDNA of human beings and viral DNA. We have studied 50 samples using the developed set. Etiology was defined in 33 samples.