Previous Article | Next Article 
J Clin Microbiol. 1987 May; 25(5): 763-767
Comparison of nasopharyngeal aspirate and nasopharyngeal swab specimens for respiratory syncytial virus diagnosis by cell culture, indirect immunofluorescence assay, and enzyme-linked immunosorbent assay.
G Ahluwalia,
J Embree,
P McNicol,
B Law and
G W Hammond
ABSTRACT
Paired nasopharyngeal aspirate (NPA) and nasopharyngeal swab (NPS) specimens obtained from each of 32 hospitalized infants with X-ray-confirmed pneumonia (91%) or bronchiolitis were tested for respiratory syncytial virus (RSV) infection by virus culture, the indirect immunofluorescent-antibody (IFA) technique, enzyme-linked immunosorbent assay (ELISA; Ortho Diagnostic Systems, Inc.), and spot hybridization with a human genomic probe to quantitate cellular DNA. RSV was isolated in cell cultures from 72% (23 of 32) of patients by using NPA specimens compared with 47% (15 of 32) by using NPS specimens. With tissue culture positivity as the reference test, the sensitivities of the ELISA on NPA and NPS specimens were found to be 69% (16 of 23) and 61% (14 of 23), respectively, with a specificity and a positive predictive value from both sites of 100%. The sensitivities of the IFA technique compared with the cell culture on NPA and NPS specimens were 61% (14 of 23) and 52% (12 of 23) with specificities of 89 and 78% and positive predictive values of 96 and 92%, respectively. Despite the recovery of significantly more cells (as shown by detection of more cellular DNA by using NPA specimens), virus was detected by the IFA technique or ELISA at similar frequencies in paired specimens. However, virus was recovered more often from NPA than NPS specimens by cell culture, and ELISA optical density readings and the number of RSV-positive fluorescing cells were greater for NPA specimens. NPA specimen collection was less traumatic for the patient, was an easier procedure for the physician to perform, and provided a superior laboratory specimen for RSV diagnosis than the NPS technique.
J Clin Microbiol. 1987 May; 25(5): 763-767
This article has been cited by other articles:
-
Abu-Diab, A., Azzeh, M., Ghneim, R., Ghneim, R., Zoughbi, M., Turkuman, S., Rishmawi, N., Issa, A.-E.-R., Siriani, I., Dauodi, R., Kattan, R., Hindiyeh, M. Y.
(2008). Comparison between Pernasal Flocked Swabs and Nasopharyngeal Aspirates for Detection of Common Respiratory Viruses in Samples from Children. J. Clin. Microbiol.
46: 2414-2417
[Abstract]
[Full Text]
-
Leland, D. S., Ginocchio, C. C.
(2007). Role of Cell Culture for Virus Detection in the Age of Technology. Clin. Microbiol. Rev.
20: 49-78
[Abstract]
[Full Text]
-
Wai, A K C, Kwok, W O, Chan, M S, Graham, C A, Rainer, T H
(2007). Patients' perceptions of nasopharyngeal aspiration in the emergency department of a teaching hospital in Hong Kong. Emerg. Med. J.
24: 35-36
[Abstract]
[Full Text]
-
Daley, P., Castriciano, S., Chernesky, M., Smieja, M.
(2006). Comparison of flocked and rayon swabs for collection of respiratory epithelial cells from uninfected volunteers and symptomatic patients.. J. Clin. Microbiol.
44: 2265-2267
[Abstract]
[Full Text]
-
Bordley, W. C., Viswanathan, M., King, V. J., Sutton, S. F., Jackman, A. M., Sterling, L., Lohr, K. N.
(2004). Diagnosis and Testing in Bronchiolitis: A Systematic Review. Arch Pediatr Adolesc Med
158: 119-126
[Abstract]
[Full Text]
-
Erdman, D. D., Weinberg, G. A., Edwards, K. M., Walker, F. J., Anderson, B. C., Winter, J., Gonzalez, M., Anderson, L. J.
(2003). GeneScan Reverse Transcription-PCR Assay for Detection of Six Common Respiratory Viruses in Young Children Hospitalized with Acute Respiratory Illness. J. Clin. Microbiol.
41: 4298-4303
[Abstract]
[Full Text]
-
Landry, M. L., Cohen, S., Ferguson, D.
(2000). Impact of Sample Type on Rapid Detection of Influenza Virus A by Cytospin-Enhanced Immunofluorescence and Membrane Enzyme-Linked Immunosorbent Assay. J. Clin. Microbiol.
38: 429-430
[Abstract]
[Full Text]
-
Covalciuc, K. A., Webb, K. H., Carlson, C. A.
(1999). Comparison of Four Clinical Specimen Types for Detection of Influenza A and B Viruses by Optical Immunoassay (FLU OIA Test) and Cell Culture Methods. J. Clin. Microbiol.
37: 3971-3974
[Abstract]
[Full Text]
-
Valarcher, J.-F., Bourhy, H., Gelfi, J., Schelcher, F.
(1999). Evaluation of a Nested Reverse Transcription-PCR Assay Based on the Nucleoprotein Gene for Diagnosis of Spontaneous and Experimental Bovine Respiratory Syncytial Virus Infections. J. Clin. Microbiol.
37: 1858-1862
[Abstract]
[Full Text]
-
Tang, Y.-W., Procop, G. W., Persing, D. H.
(1997). Molecular diagnostics of infectious diseases. Clin. Chem.
43: 2021-2038
[Abstract]
[Full Text]
-
Marks, M. I.
(1992). Respiratory Syncytial Virus Infections. CLIN PEDIATR
31: 688-691
Copyright © 1987 by the American Society for Microbiology. All rights reserved.