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Journal of Clinical Microbiology logoLink to Journal of Clinical Microbiology
. 1995 Oct;33(10):2535–2542. doi: 10.1128/jcm.33.10.2535-2542.1995

Recombinant mono- and polyantigens to detect cytomegalovirus-specific immunoglobulin M in human sera by enzyme immunoassay.

M P Landini 1, T Lazzarotto 1, G T Maine 1, A Ripalti 1, R Flanders 1
PMCID: PMC228524  PMID: 8567879

Abstract

Serological detection of human cytomegalovirus (HCMV)-specific antibody varies greatly because of antigen composition and the lack of antigen standardization. Antigenic materials composed of single well-characterized viral proteins or portions of them, produced via molecular biology, have proven to be promising tools in improving serodiagnosis. We constructed a recombinant protein containing two regions of ppUL32 (p150) and half of ppUL44 (p52) and compared the immunoglobulin M (IgM) reactivity of this triple-antigen fusion protein with that of a double-antigen fusion protein containing the two ppUL32 fragments and that of a monoantigen fusion protein containing half of ppUL44. We also constructed and tested two other monoantigen fusion proteins containing a large fraction of ppUL80a and a fraction of ppUL83. More than 700 serum samples from different groups of immunocompetent and immunosuppressed subjects were tested for the presence of HCMV IgM by recombinant enzyme immunoassay (rec-EIA) and by a commercially available EIA. Western blotting (immunoblotting) and (in the case of immunosuppressed individuals) antigenemia tests by immunofluorescence and PCR of polymorphonuclear leukocytes were also carried out. The results obtained demonstrate that (i) the triple-antigen fusion protein can replace the individual proteins; (ii) the triple-antigen fusion protein cannot be used alone to replace the virus or infected cells in the serological detection of anti-CMV IgM; (iii) the addition of the fusion proteins containing portions of ppUL83 and ppUL80a is essential for the formation of an antigenic mixture that can replace the virus for the search of HCMV-specific IgM; (iv) rec-EIA is very specific and is more sensitive than the commercially available EIA, and the results obtained are consistent with those obtained by Western blotting; and (v) rec-EIA can reliably be used to detect HCMV-specific IgM in different groups of patients with active HCMV infection.

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Selected References

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  1. Alford C. A., Hayes K., Britt W. Primary cytomegalovirus infection in pregnancy: comparison of antibody responses to virus-encoded proteins between women with and without intrauterine infection. J Infect Dis. 1988 Nov;158(5):917–924. doi: 10.1093/infdis/158.5.917. [DOI] [PubMed] [Google Scholar]
  2. Basson J., Tardy J. C., Aymard M. Pattern of anti-cytomegalovirus IgM antibodies determined by immunoblotting. A study of kidney graft recipients developing a primary or recurrent CMV infection. Arch Virol. 1989;108(3-4):259–270. doi: 10.1007/BF01310938. [DOI] [PubMed] [Google Scholar]
  3. Boland G. J., de Gast G. C., Hené R. J., Jambroes G., Donckerwolcke R., The T. H., Mudde G. C. Early detection of active cytomegalovirus (CMV) infection after heart and kidney transplantation by testing for immediate early antigenemia and influence of cellular immunity on the occurrence of CMV infection. J Clin Microbiol. 1990 Sep;28(9):2069–2075. doi: 10.1128/jcm.28.9.2069-2075.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bolling T. J., Mandecki W. An Escherichia coli expression vector for high-level production of heterologous proteins in fusion with CMP-KDO synthetase. Biotechniques. 1990 May;8(5):488–492. [PubMed] [Google Scholar]
  5. Dolan J., Briggs J. D., Clements G. B. Antibodies to cytomegalovirus in renal allograft recipients: correlation with isolation of virus. J Clin Pathol. 1989 Oct;42(10):1070–1077. doi: 10.1136/jcp.42.10.1070. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. 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]
  7. Gold D., Ashley R., Handsfield H. H., Verdon M., Leach L., Mills J., Drew L., Corey L. Immunoblot analysis of the humoral immune response in primary cytomegalovirus infection. J Infect Dis. 1988 Feb;157(2):319–326. doi: 10.1093/infdis/157.2.319. [DOI] [PubMed] [Google Scholar]
  8. Grazia Revello M., Zavattoni M., Percivalle E., Grossi P., Gerna G. Correlation between immunofluorescent detection of human cytomegalovirus immediate early antigens in polymorphonuclear leukocytes and viremia. J Infect Dis. 1989 Jul;160(1):159–160. doi: 10.1093/infdis/160.1.159. [DOI] [PubMed] [Google Scholar]
  9. Jahn G., Kouzarides T., Mach M., Scholl B. C., Plachter B., Traupe B., Preddie E., Satchwell S. C., Fleckenstein B., Barrell B. G. Map position and nucleotide sequence of the gene for the large structural phosphoprotein of human cytomegalovirus. J Virol. 1987 May;61(5):1358–1367. doi: 10.1128/jvi.61.5.1358-1367.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. 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]
  11. Jiwa N. M., Van Gemert G. W., Raap A. K., Van de Rijke F. M., Mulder A., Lens P. F., Salimans M. M., Zwaan F. E., Van Dorp W., Van der Ploeg M. Rapid detection of human cytomegalovirus DNA in peripheral blood leukocytes of viremic transplant recipients by the polymerase chain reaction. Transplantation. 1989 Jul;48(1):72–76. doi: 10.1097/00007890-198907000-00017. [DOI] [PubMed] [Google Scholar]
  12. Karlin S., Mocarski E. S., Schachtel G. A. Molecular evolution of herpesviruses: genomic and protein sequence comparisons. J Virol. 1994 Mar;68(3):1886–1902. doi: 10.1128/jvi.68.3.1886-1902.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Landini M. P., Guan M. X., Jahn G., Lindenmaier W., Mach M., Ripalti A., Necker A., Lazzarotto T., Plachter B. Large-scale screening of human sera with cytomegalovirus recombinant antigens. J Clin Microbiol. 1990 Jun;28(6):1375–1379. doi: 10.1128/jcm.28.6.1375-1379.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Landini M. P., Lazzarotto T., Ripalti A., Guan M. X., La Placa M. Antibody response to recombinant lambda gt11 fusion proteins in cytomegalovirus infection. J Clin Microbiol. 1989 Oct;27(10):2324–2327. doi: 10.1128/jcm.27.10.2324-2327.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Landini M. P. New approaches and perspectives in cytomegalovirus diagnosis. Prog Med Virol. 1993;40:157–177. [PubMed] [Google Scholar]
  16. Landini M. P., Re M. C., Mirolo G., Baldassarri B., La Placa M. Human immune response to cytomegalovirus structural polypeptides studied by immunoblotting. J Med Virol. 1985 Dec;17(4):303–311. doi: 10.1002/jmv.1890170403. [DOI] [PubMed] [Google Scholar]
  17. Landini M. P., Ripalti A., Sra K., Pouletty P. Human cytomegalovirus structural proteins: immune reaction against pp150 synthetic peptides. J Clin Microbiol. 1991 Sep;29(9):1868–1872. doi: 10.1128/jcm.29.9.1868-1872.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Lazzarotto T., Dalla Casa B., Campisi B., Landini M. P. Enzyme-linked immunoadsorbent assay for the detection of cytomegalovirus-IgM: comparison between eight commercial kits, immunofluorescence, and immunoblotting. J Clin Lab Anal. 1992;6(4):216–218. doi: 10.1002/jcla.1860060409. [DOI] [PubMed] [Google Scholar]
  19. Lazzarotto T., Furlini G., Re M. C., Ramazzotti E., Campisi B., Landini M. P. Human cytomegalovirus replication correlates with differentiation in a hematopoietic progenitor cell line and can be modulated by HIV-1. Arch Virol. 1994;135(1-2):13–28. doi: 10.1007/BF01309762. [DOI] [PubMed] [Google Scholar]
  20. Marsano L., Perrillo R. P., Flye M. W., Hanto D. W., Spitzer E. D., Thomas J. R., Murray P. R., Windus D. W., Brunt E. M., Storch G. A. Comparison of culture and serology for the diagnosis of cytomegalovirus infection in kidney and liver transplant recipients. J Infect Dis. 1990 Mar;161(3):454–461. doi: 10.1093/infdis/161.3.454. [DOI] [PubMed] [Google Scholar]
  21. Nielsen S. L., Sørensen I., Andersen H. K. Kinetics of specific immunoglobulins M, E, A, and G in congenital, primary, and secondary cytomegalovirus infection studied by antibody-capture enzyme-linked immunosorbent assay. J Clin Microbiol. 1988 Apr;26(4):654–661. doi: 10.1128/jcm.26.4.654-661.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Novák J., Sova P., Krchnák V., Hamsíková E., Závadová H., Roubal J. Mapping of serologically relevant regions of human cytomegalovirus phosphoprotein pp150 using synthetic peptides. J Gen Virol. 1991 Jun;72(Pt 6):1409–1413. doi: 10.1099/0022-1317-72-6-1409. [DOI] [PubMed] [Google Scholar]
  23. Plachter B., Wieczorek L., Scholl B. C., Ziegelmaier R., Jahn G. Detection of cytomegalovirus antibodies by an enzyme-linked immunosorbent assay using recombinant polypeptides of the large phosphorylated tegument protein pp150. J Clin Microbiol. 1992 Jan;30(1):201–206. doi: 10.1128/jcm.30.1.201-206.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Ripalti A., Boccuni M. C., Campanini F., Bergamini G., Lazzarotto T., Battista M. C., Dalla Casa B., Landini M. P. Construction of a polyepitope fusion antigen of human cytomegalovirus ppUL32 and detection of specific antibodies by ELISA. New Microbiol. 1995 Jan;18(1):1–12. [PubMed] [Google Scholar]
  25. Ripalti A., Dal Monte P., Boccuni M. C., Campanini F., Lazzarotto T., Campisi B., Ruan Q., Landini M. P. Prokaryotic expression of a large fragment of the most antigenic cytomegalovirus DNA-binding protein (ppUL44) and its reactivity with human antibodies. J Virol Methods. 1994 Jan;46(1):39–50. doi: 10.1016/0166-0934(94)90015-9. [DOI] [PubMed] [Google Scholar]
  26. Ripalti A., Landini M. P., Mocarski E. S., La Placa M. Identification and preliminary use of recombinant lambda gt11 fusion proteins in human cytomegalovirus diagnosis. J Gen Virol. 1989 May;70(Pt 5):1247–1251. doi: 10.1099/0022-1317-70-5-1247. [DOI] [PubMed] [Google Scholar]
  27. Ripalti A., Ruan Q., Boccuni M. C., Campanini F., Bergamini G., Landini M. P. Construction of polyepitope fusion antigens of human cytomegalovirus ppUL32: reactivity with human antibodies. J Clin Microbiol. 1994 Feb;32(2):358–363. doi: 10.1128/jcm.32.2.358-363.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Robinson J. M., Pilot-Matias T. J., Pratt S. D., Patel C. B., Bevirt T. S., Hunt J. C. Analysis of the humoral response to the flagellin protein of Borrelia burgdorferi: cloning of regions capable of differentiating Lyme disease from syphilis. J Clin Microbiol. 1993 Mar;31(3):629–635. doi: 10.1128/jcm.31.3.629-635.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. 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]
  30. Vornhagen R., Plachter B., Hinderer W., The T. H., Van Zanten J., Matter L., Schmidt C. A., Sonneborn H. H., Jahn G. Early serodiagnosis of acute human cytomegalovirus infection by enzyme-linked immunosorbent assay using recombinant antigens. J Clin Microbiol. 1994 Apr;32(4):981–986. doi: 10.1128/jcm.32.4.981-986.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. van der Bij W., Torensma R., van Son W. J., Anema J., Schirm J., Tegzess A. M., The T. H. Rapid immunodiagnosis of active cytomegalovirus infection by monoclonal antibody staining of blood leucocytes. J Med Virol. 1988 Jun;25(2):179–188. doi: 10.1002/jmv.1890250208. [DOI] [PubMed] [Google Scholar]

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