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Direct diagnosis of human respiratory coronaviruses 229E and OC43 by the polymerase chain reaction

An RT-PCR-hybridization was developed that amplified genetic material from the M protein gene of HCoV-229E and HCoV-OC43. The analytic sensitivity of these original primers were compared with primers defined in the N gene and described previously. The results show that 0.05 TCID(50) of HCoV-229E and...

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Detalles Bibliográficos
Autores principales: Vabret, Astrid, Mouthon, Franck, Mourez, Thomas, Gouarin, Stephanie, Petitjean, Joëlle, Freymuth, François
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science B.V. 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7119936/
https://www.ncbi.nlm.nih.gov/pubmed/11483217
http://dx.doi.org/10.1016/S0166-0934(01)00343-3
Descripción
Sumario:An RT-PCR-hybridization was developed that amplified genetic material from the M protein gene of HCoV-229E and HCoV-OC43. The analytic sensitivity of these original primers were compared with primers defined in the N gene and described previously. The results show that 0.05 TCID(50) of HCoV-229E and 0.01 TCID(50) of HCoV-OC43 can be detected by this molecular method using the original method. Detection of HCoV-229E and HCoV-OC43 in clinical specimens is possible using this method: 348 respiratory specimens (202 sputum and 146 nasal aspirates) were tested with this RT-PCR-hybridization and 12 human coronavirus are detected (3%). The method could provide a useful tool for demonstrating the role of human coronavirus in infections of the respiratory tract.