Skip to main content
Journal of Clinical Microbiology logoLink to Journal of Clinical Microbiology
. 1992 Mar;30(3):685–690. doi: 10.1128/jcm.30.3.685-690.1992

Detection of cytomegalovirus in urine samples by an enzyme-linked immunosorbent assay using a monoclonal antibody against the viral 150-kilodalton protein.

T Yamanaka 1, K Kiyotani 1, T Sakaguchi 1, Y Fukuda 1, K Dohi 1, M Yamada 1, M Yoshida 1, S Nii 1, T Yoshida 1
PMCID: PMC265133  PMID: 1313048

Abstract

McKeating et al. (J.A. McKeating, P.D. Griffiths, and J.E. Grundy, J. Gen. Virol. 68:785-792, 1987; J. A. McKeating, J. E. Grundy, Z. Varghese, and P. D. Griffiths, J. Med. Virol. 18:341-348, 1986; J. A. McKeating, S. Stagno, P. R. Stirk, and P. D. Griffiths, J. Med. Virol. 16:367-373, 1985) reported previously that beta 2 microglobulin inhibits the detection of human cytomegalovirus (CMV) in urine specimens by an enzyme-linked immunosorbent assay (ELISA) with a monoclonal antibody against the glycoprotein of CMV. They postulated that beta 2 microglobulin binds to the viral glycoproteins and masks the antigenic determinants. We developed here an ELISA method for the detection of CMV in urine by using a monoclonal antibody against the viral 150-kDa protein to capture the viral antigen. This assay detected CMV both in culture medium and in urine specifically at concentrations higher than 10(3) PFU/ml and quantitatively at concentrations higher than 10(4) PFU/ml. The sensitivity of the ELISA increased about 10-fold when peroxidase-labeled F(ab')2 from goat anti-human immunoglobulin G was used as a secondary detecting antibody in combination with concentration of the virus in urine samples by ultracentrifugation. The inhibition of ELISA by beta 2 microglobulin was not observed in this ELISA system. When 56 urine specimens from renal transplant recipients were examined for CMV antigens, the ELISA system had a sensitivity of 78% and a specificity of 97%. The positive and negative predictive values of the assay were 95 and 86%, respectively. Furthermore, CMV antigens in urine were quantitated by the assay during the course of typical CMV disease of renal transplant recipient. These results suggest strongly that the measurement of CMV antigens in urine by our rapid and quantitative ELISA system provides very useful data for the monitoring of CMV infections in renal transplant recipients and making decisions about therapy.

Full text

PDF
685

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Demmler G. J., Buffone G. J., Schimbor C. M., May R. A. Detection of cytomegalovirus in urine from newborns by using polymerase chain reaction DNA amplification. J Infect Dis. 1988 Dec;158(6):1177–1184. doi: 10.1093/infdis/158.6.1177. [DOI] [PubMed] [Google Scholar]
  2. Gibson W. Protein counterparts of human and simian cytomegaloviruses. Virology. 1983 Jul 30;128(2):391–406. doi: 10.1016/0042-6822(83)90265-9. [DOI] [PubMed] [Google Scholar]
  3. Gleaves C. A., Smith T. F., Shuster E. A., Pearson G. R. Rapid detection of cytomegalovirus in MRC-5 cells inoculated with urine specimens by using low-speed centrifugation and monoclonal antibody to an early antigen. J Clin Microbiol. 1984 Jun;19(6):917–919. doi: 10.1128/jcm.19.6.917-919.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Grundy J. E., McKeating J. A., Griffiths P. D. Cytomegalovirus strain AD169 binds beta 2 microglobulin in vitro after release from cells. J Gen Virol. 1987 Mar;68(Pt 3):777–784. doi: 10.1099/0022-1317-68-3-777. [DOI] [PubMed] [Google Scholar]
  5. Hsia K., Spector D. H., Lawrie J., Spector S. A. Enzymatic amplification of human cytomegalovirus sequences by polymerase chain reaction. J Clin Microbiol. 1989 Aug;27(8):1802–1809. doi: 10.1128/jcm.27.8.1802-1809.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Inoue Y., Ohashi Y., Shimomura Y., Manabe R., Yamada M., Ueda S., Kato S. Herpes simplex virus glycoprotein D. Protective immunity against murine herpetic keratitis. Invest Ophthalmol Vis Sci. 1990 Mar 1;31(3):411–418. [PubMed] [Google Scholar]
  7. Jahn G., Mach M. Human cytomegalovirus phosphoproteins and glycoproteins and their coding regions. Curr Top Microbiol Immunol. 1990;154:171–185. doi: 10.1007/978-3-642-74980-3_7. [DOI] [PubMed] [Google Scholar]
  8. Jahn G., Scholl B. C., Traupe B., Fleckenstein B. The two major structural phosphoproteins (pp65 and pp150) of human cytomegalovirus and their antigenic properties. J Gen Virol. 1987 May;68(Pt 5):1327–1337. doi: 10.1099/0022-1317-68-5-1327. [DOI] [PubMed] [Google Scholar]
  9. McKeating J. A., Griffiths P. D., Grundy J. E. Cytomegalovirus in urine specimens has host beta 2 microglobulin bound to the viral envelope: a mechanism of evading the host immune response? J Gen Virol. 1987 Mar;68(Pt 3):785–792. doi: 10.1099/0022-1317-68-3-785. [DOI] [PubMed] [Google Scholar]
  10. McKeating J. A., Grundy J. E., Varghese Z., Griffiths P. D. Detection of cytomegalovirus by ELISA in urine samples is inhibited by beta 2 microglobulin. J Med Virol. 1986 Apr;18(4):341–348. doi: 10.1002/jmv.1890180407. [DOI] [PubMed] [Google Scholar]
  11. McKeating J. A., Stagno S., Stirk P. R., Griffiths P. D. Detection of cytomegalovirus in urine samples by enzyme-linked immunosorbent assay. J Med Virol. 1985 Aug;16(4):367–373. doi: 10.1002/jmv.1890160410. [DOI] [PubMed] [Google Scholar]
  12. Olive D. M., Simsek M., Al-Mufti S. Polymerase chain reaction assay for detection of human cytomegalovirus. J Clin Microbiol. 1989 Jun;27(6):1238–1242. doi: 10.1128/jcm.27.6.1238-1242.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Pronovost A. D., Baumgarten A., Andiman W. A. Chemiluminescent immunoenzymatic assay for rapid diagnosis of viral infections. J Clin Microbiol. 1982 Aug;16(2):345–349. doi: 10.1128/jcm.16.2.345-349.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Roby C., Gibson W. Characterization of phosphoproteins and protein kinase activity of virions, noninfectious enveloped particles, and dense bodies of human cytomegalovirus. J Virol. 1986 Sep;59(3):714–727. doi: 10.1128/jvi.59.3.714-727.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Rudolph S. A., Kühn J. E., Korn K., Braun R. W., Jahn G. Prokaryotic expression of the major capsid protein of human cytomegalovirus and antigenic cross-reactions with herpes simplex virus type 1. J Gen Virol. 1990 Sep;71(Pt 9):2023–2031. doi: 10.1099/0022-1317-71-9-2023. [DOI] [PubMed] [Google Scholar]
  16. Scholl B. C., Von Hintzenstern J., Borisch B., Traupe B., Bröker M., Jahn G. Prokaryotic expression of immunogenic polypeptides of the large phosphoprotein (pp150) of human cytomegalovirus. J Gen Virol. 1988 Jun;69(Pt 6):1195–1204. doi: 10.1099/0022-1317-69-6-1195. [DOI] [PubMed] [Google Scholar]
  17. Shibata D., Martin W. J., Appleman M. D., Causey D. M., Leedom J. M., Arnheim N. Detection of cytomegalovirus DNA in peripheral blood of patients infected with human immunodeficiency virus. J Infect Dis. 1988 Dec;158(6):1185–1192. doi: 10.1093/infdis/158.6.1185. [DOI] [PubMed] [Google Scholar]
  18. Stanier P., Taylor D. L., Kitchen A. D., Wales N., Tryhorn Y., Tyms A. S. Persistence of cytomegalovirus in mononuclear cells in peripheral blood from blood donors. BMJ. 1989 Oct 7;299(6704):897–898. doi: 10.1136/bmj.299.6704.897. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Yolken R. H. Enzyme immunoassays for the detection of infectious antigens in body fluids: current limitations and future prospects. Rev Infect Dis. 1982 Jan-Feb;4(1):35–68. doi: 10.1093/clinids/4.1.35. [DOI] [PubMed] [Google Scholar]
  20. Yolken R. H., Stopa P. J. Comparison of seven enzyme immunoassay systems for measurement of cytomegalovirus. J Clin Microbiol. 1980 Jun;11(6):546–551. doi: 10.1128/jcm.11.6.546-551.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. el-Mekki A., Al-Nakib W., Bibi R. Factors affecting the detection of cytomegalovirus in urine by sandwich enzyme immunoassays. J Virol Methods. 1987 Jan;15(1):75–83. doi: 10.1016/0166-0934(87)90050-4. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Clinical Microbiology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES