Rapid culture-amplified immunofluorescent test for the detection of human rhinoviruses in clinical samples: Evidence of a common epitope in culture
Autor: | A. El Mekki, W. Al-Mulla, W. Al-Nakib |
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Rok vydání: | 1994 |
Předmět: |
Serotype
Rhinovirus Common Cold Fluorescent Antibody Technique Enzyme-Linked Immunosorbent Assay Nose medicine.disease_cause Immunofluorescence Epitope Virus Specimen Handling Epitopes stomatognathic system Antigen Virology otorhinolaryngologic diseases medicine Humans Antigens Viral medicine.diagnostic_test biology virus diseases Common cold medicine.disease Infectious Diseases Kuwait Polyclonal antibodies biology.protein HeLa Cells |
Zdroj: | Journal of Medical Virology. 42:182-187 |
ISSN: | 1096-9071 0146-6615 |
DOI: | 10.1002/jmv.1890420215 |
Popis: | Ohio HeLa cells in multichamber slides were inoculated with nasal samples from patients presenting with common cold symptoms and incubated at 33 degrees C with gentle shaking for 48 hours. The cultures were fixed with cold acetone, and viral antigens were detected by immunofluorescence using an antirhinovirus type 2 (HRV-2) polyclonal serum. Of 158 samples, 58 (36.7%) and 57 (36%) were positive for HRV by virus isolation (confirmed by acid lability test) and by culture-amplified immunofluorescent (CAIF) test, respectively. The correlation between the two tests was highly significant (P = 0.0001). Nasal washings or nasal/throat swabs were equally suitable for detecting virus by isolation but not by CAIF. On the other hand, nasal washings were better than nasal/throat swabs for detecting HRV by CAIF. In an ELISA system, the polyclonal anti-HRV-2 serum recognized a rhinovirus antigen expressed in situ within 48 hr postinfection by all the 11 HRV serotypes investigated. However, 60 hr postinfection, the anti-HRV-2 serum recognized only homologous and closely related HRV antigens. These results suggest that a rhinovirus "common" antigen may be expressed some 48 hr after infection of Ohio HeLa cells with rhinoviruses. The CAIF test provides a sensitive, rapid and reliable procedure to detect wild-type rhinovirus infection as well as a clear alternative to detection by isolation. |
Databáze: | OpenAIRE |
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