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New and sensitive standard cell culture technique for the detection of cytomegalovirus in clinical specimens
Author(s) -
Agha S. A.,
Coleman J. C.,
Mahmoud L. A.,
AbdElaal A. M.,
Selwyn S.
Publication year - 1988
Publication title -
journal of medical virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.782
H-Index - 121
eISSN - 1096-9071
pISSN - 0146-6615
DOI - 10.1002/jmv.1890260112
Subject(s) - cytopathic effect , human cytomegalovirus , cell culture , centrifugation , immunofluorescence , vial , virology , microbiology and biotechnology , biology , cell , sonication , cytomegalovirus , virus , chemistry , chromatography , antibody , herpesviridae , immunology , viral disease , genetics
Conventional tube cell culture has been recognised as the most sensitive technique available for human cytomegalovirus (HCMV) detection. Low‐speed centrifugation of specimen inocula onto cell culture monolayers has been shown to increase the efficiency of infection with the AD 169 strain of HCMV. Therefore a centrifugal force of 900g for 1 hour at 37°C was used to enhance the detection of HCMV cytopathic effect (CPE) in shell vials that contained circular coverslips with a monolayer of human embryonic lung (HEL) fibroblasts. Of 195 specimens, HCMV CPE was detected in 18 specimens (9.02%) on shell vial culture assay, whereas conventional tube cell culture was positive in only 13 specimens (6.6%). The shell vial culture assay was significantly more sensitive ( P < 0.05). Furthermore the development of the cytopathic effect on shell vial culture assay was significantly earlier ( P < 0.01) and more extensive. Urine samples were sonicated and the results obtained with immunofluorescence using human immune serum demonstrated that sonication increased both the intensity of fluorescence and number of fluorescent foci of HCMV‐infected cells and also decreased the nonspecific fluorescence of the background.