Woodtayakorn J, Punnarugsa V
Department of Microbiology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Asian Pac J Allergy Immunol. 1991 Dec;9(2):121-4.
133 nasopharyngeal aspirates (NPA) were simultaneously tested for the presence of respiratory syncytial virus (RSV) by conventional cell culture (CCC), shell vial centrifugation culture (SVC), immunofluorescence assay (IFA) and biotin-avidin enzyme linked immunosorbent assay (B-A ELISA). These yielded positive results in 32(24%), 45(33.8%), 36(27%) and 40(30%) of specimens, respectively. Specimens positive by IFA and B-A ELISA were all also positive by SVC. The sensitivity of CCC, IFA, and B-A ELISA comparing to SVC was 71%, 80%, and 88.9%, respectively. For rapid detection of RSV, we recommend the SVC method where a cell culture laboratory is available and the B-A ELISA method where a cell culture laboratory is not available.
采用常规细胞培养(CCC)、空斑小室离心培养(SVC)、免疫荧光测定法(IFA)和生物素-抗生物素蛋白酶联免疫吸附测定法(B-A ELISA),同时对133份鼻咽抽吸物(NPA)进行呼吸道合胞病毒(RSV)检测。这些方法分别在32份(24%)、45份(33.8%)、36份(27%)和40份(30%)标本中检测出阳性结果。免疫荧光测定法和生物素-抗生物素蛋白酶联免疫吸附测定法检测出的阳性标本,空斑小室离心培养法检测也均为阳性。与空斑小室离心培养法相比,常规细胞培养法、免疫荧光测定法和生物素-抗生物素蛋白酶联免疫吸附测定法的灵敏度分别为71%、80%和88.9%。对于呼吸道合胞病毒的快速检测,我们建议,在有细胞培养实验室的情况下采用空斑小室离心培养法,在没有细胞培养实验室的情况下采用生物素-抗生物素蛋白酶联免疫吸附测定法。