Skip to main content
Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1991 Jul 1;88(13):5922–5926. doi: 10.1073/pnas.88.13.5922

Differentiation between two distinct classes of viruses now classified as human herpesvirus 6.

E C Schirmer 1, L S Wyatt 1, K Yamanishi 1, W J Rodriguez 1, N Frenkel 1
PMCID: PMC51990  PMID: 1648234

Abstract

Human herpesvirus 6 (HHV-6) causes exanthem subitum (ES, roseola infantum), a childhood disease characterized by high fever and skin rash. We have analyzed restriction enzyme cleavage patterns of the DNAs of ES virus isolates from Japan and the United States. The patterns of all the ES viral DNAs were highly conserved, except for variable sequences within the terminal repeat sequences. They resembled closely the restriction enzyme patterns of the Z29 strain of HHV-6 but were distinct from those of the U1102 strain. That all ES isolates were closely related whereas the U1102 patterns were very different suggests that the U1102 strain represents a distinct virus. Moreover, the ES isolates all resembled the Z29 strain and not the U1102 strain with respect to reactivity with HHV-6 monoclonal antibodies. These findings provide evidence for the existence of two distinct classes of viruses previously classified as HHV-6. Whereas the Z29-like viruses are involved in ES infections, the association of the U1102-like viruses with human disease has yet to be determined.

Full text

PDF
5922

Images in this article

Selected References

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

  1. Ablashi D. V., Lusso P., Hung C. L., Salahuddin S. Z., Josephs S. F., Llana T., Kramarsky B., Biberfeld P., Markham P. D., Gallo R. C. Utilization of human hematopoietic cell lines for the propagation and characterization of HBLV (human herpesvirus 6). Int J Cancer. 1988 Nov 15;42(5):787–791. doi: 10.1002/ijc.2910420526. [DOI] [PubMed] [Google Scholar]
  2. Agut H., Guetard D., Collandre H., Dauguet C., Montagnier L., Miclea J. M., Baurmann H., Gessain A. Concomitant infection by human herpesvirus 6, HTLV-I, and HIV-2. Lancet. 1988 Mar 26;1(8587):712–712. doi: 10.1016/s0140-6736(88)91520-6. [DOI] [PubMed] [Google Scholar]
  3. Asano Y., Yoshikawa T., Suga S., Yazaki T., Kondo K., Yamanishi K. Fatal fulminant hepatitis in an infant with human herpesvirus-6 infection. Lancet. 1990 Apr 7;335(8693):862–863. doi: 10.1016/0140-6736(90)90983-c. [DOI] [PubMed] [Google Scholar]
  4. Balachandran N., Amelse R. E., Zhou W. W., Chang C. K. Identification of proteins specific for human herpesvirus 6-infected human T cells. J Virol. 1989 Jun;63(6):2835–2840. doi: 10.1128/jvi.63.6.2835-2840.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Becker W. B., Engelbrecht S., Becker M. L., Piek C., Robson B. A., Wood L., Jacobs P. New T-lymphotropic human herpesviruses. Lancet. 1989 Jan 7;1(8628):41–41. doi: 10.1016/s0140-6736(89)91691-7. [DOI] [PubMed] [Google Scholar]
  6. Black J. B., Sanderlin K. C., Goldsmith C. S., Gary H. E., Lopez C., Pellett P. E. Growth properties of human herpesvirus-6 strain Z29. J Virol Methods. 1989 Nov;26(2):133–145. doi: 10.1016/0166-0934(89)90143-2. [DOI] [PubMed] [Google Scholar]
  7. Buchman T. G., Simpson T., Nosal C., Roizman B., Nahmias A. J. The structure of herpes simplex virus DNA and its application to molecular epidemiology. Ann N Y Acad Sci. 1980;354:279–290. doi: 10.1111/j.1749-6632.1980.tb27972.x. [DOI] [PubMed] [Google Scholar]
  8. Di Luca D., Katsafanas G., Schirmer E. C., Balachandran N., Frenkel N. The replication of viral and cellular DNA in human herpesvirus 6-infected cells. Virology. 1990 Mar;175(1):199–210. doi: 10.1016/0042-6822(90)90200-b. [DOI] [PubMed] [Google Scholar]
  9. Downing R. G., Sewankambo N., Serwadda D., Honess R., Crawford D., Jarrett R., Griffin B. E. Isolation of human lymphotropic herpesviruses from Uganda. Lancet. 1987 Aug 15;2(8555):390–390. doi: 10.1016/s0140-6736(87)92403-2. [DOI] [PubMed] [Google Scholar]
  10. Frenkel N., Schirmer E. C., Wyatt L. S., Katsafanas G., Roffman E., Danovich R. M., June C. H. Isolation of a new herpesvirus from human CD4+ T cells. Proc Natl Acad Sci U S A. 1990 Jan;87(2):748–752. doi: 10.1073/pnas.87.2.748. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Harnett G. B., Farr T. J., Pietroboni G. R., Bucens M. R. Frequent shedding of human herpesvirus 6 in saliva. J Med Virol. 1990 Feb;30(2):128–130. doi: 10.1002/jmv.1890300209. [DOI] [PubMed] [Google Scholar]
  12. Irving W. L., Cunningham A. L., Keogh A., Chapman J. R. Antibody to both human herpesvirus 6 and cytomegalovirus. Lancet. 1988 Sep 10;2(8611):630–631. doi: 10.1016/s0140-6736(88)90669-1. [DOI] [PubMed] [Google Scholar]
  13. Jarrett R. F., Gallagher A., Gledhill S., Jones M. D., Teo I., Griffin B. E. Variation in restriction map of MHV-6 genome. Lancet. 1989 Feb 25;1(8635):448–449. doi: 10.1016/s0140-6736(89)90052-4. [DOI] [PubMed] [Google Scholar]
  14. Josephs S. F., Ablashi D. V., Salahuddin S. Z., Kramarsky B., Franza B. R., Jr, Pellett P., Buchbinder A., Memon S., Wong-Staal F., Gallo R. C. Molecular studies of HHV-6. J Virol Methods. 1988 Sep;21(1-4):179–190. doi: 10.1016/0166-0934(88)90064-x. [DOI] [PubMed] [Google Scholar]
  15. Josephs S. F., Salahuddin S. Z., Ablashi D. V., Schachter F., Wong-Staal F., Gallo R. C. Genomic analysis of the human B-lymphotropic virus (HBLV). Science. 1986 Oct 31;234(4776):601–603. doi: 10.1126/science.3020691. [DOI] [PubMed] [Google Scholar]
  16. Kikuta H., Lu H., Matsumoto S., Josephs S. F., Gallo R. C. Polymorphism of human herpesvirus 6 DNA from five Japanese patients with exanthem subitum. J Infect Dis. 1989 Sep;160(3):550–551. doi: 10.1093/infdis/160.3.550. [DOI] [PubMed] [Google Scholar]
  17. Kurata T., Iwasaki T., Sata T., Wakabayashi T., Yamaguchi K., Okuno T., Yamanishi K., Takei Y. Viral pathology of human herpesvirus 6 infection. Adv Exp Med Biol. 1990;278:39–47. doi: 10.1007/978-1-4684-5853-4_5. [DOI] [PubMed] [Google Scholar]
  18. Levy J. A., Ferro F., Greenspan D., Lennette E. T. Frequent isolation of HHV-6 from saliva and high seroprevalence of the virus in the population. Lancet. 1990 May 5;335(8697):1047–1050. doi: 10.1016/0140-6736(90)92628-u. [DOI] [PubMed] [Google Scholar]
  19. Lopez C., Pellett P., Stewart J., Goldsmith C., Sanderlin K., Black J., Warfield D., Feorino P. Characteristics of human herpesvirus-6. J Infect Dis. 1988 Jun;157(6):1271–1273. doi: 10.1093/infdis/157.6.1271. [DOI] [PubMed] [Google Scholar]
  20. Okuno T., Higashi K., Shiraki K., Yamanishi K., Takahashi M., Kokado Y., Ishibashi M., Takahara S., Sonoda T., Tanaka K. Human herpesvirus 6 infection in renal transplantation. Transplantation. 1990 Mar;49(3):519–522. doi: 10.1097/00007890-199003000-00009. [DOI] [PubMed] [Google Scholar]
  21. Okuno T., Takahashi K., Balachandra K., Shiraki K., Yamanishi K., Takahashi M., Baba K. Seroepidemiology of human herpesvirus 6 infection in normal children and adults. J Clin Microbiol. 1989 Apr;27(4):651–653. doi: 10.1128/jcm.27.4.651-653.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Pellett P. E., Lindquester G. J., Feorino P., Lopez C. Genomic heterogeneity of human herpesvirus 6 isolates. Adv Exp Med Biol. 1990;278:9–18. doi: 10.1007/978-1-4684-5853-4_2. [DOI] [PubMed] [Google Scholar]
  23. Pietroboni G. R., Harnett G. B., Bucens M. R., Honess R. W. Isolation of human herpesvirus 6 from saliva. Lancet. 1988 May 7;1(8593):1059–1059. doi: 10.1016/s0140-6736(88)91884-3. [DOI] [PubMed] [Google Scholar]
  24. Salahuddin S. Z., Ablashi D. V., Markham P. D., Josephs S. F., Sturzenegger S., Kaplan M., Halligan G., Biberfeld P., Wong-Staal F., Kramarsky B. Isolation of a new virus, HBLV, in patients with lymphoproliferative disorders. Science. 1986 Oct 31;234(4776):596–601. doi: 10.1126/science.2876520. [DOI] [PubMed] [Google Scholar]
  25. Saxinger C., Polesky H., Eby N., Grufferman S., Murphy R., Tegtmeir G., Parekh V., Memon S., Hung C. Antibody reactivity with HBLV (HHV-6) in U.S. populations. J Virol Methods. 1988 Sep;21(1-4):199–208. doi: 10.1016/0166-0934(88)90066-3. [DOI] [PubMed] [Google Scholar]
  26. Tajiri H., Nose O., Baba K., Okada S. Human herpesvirus-6 infection with liver injury in neonatal hepatitis. Lancet. 1990 Apr 7;335(8693):863–863. doi: 10.1016/0140-6736(90)90984-d. [DOI] [PubMed] [Google Scholar]
  27. Tedder R. S., Briggs M., Cameron C. H., Honess R., Robertson D., Whittle H. A novel lymphotropic herpesvirus. Lancet. 1987 Aug 15;2(8555):390–392. doi: 10.1016/s0140-6736(87)92404-4. [DOI] [PubMed] [Google Scholar]
  28. Ueda K., Kusuhara K., Hirose M., Okada K., Miyazaki C., Tokugawa K., Nakayama M., Yamanishi K. Exanthem subitum and antibody to human herpesvirus-6. J Infect Dis. 1989 Apr;159(4):750–752. doi: 10.1093/infdis/159.4.750. [DOI] [PubMed] [Google Scholar]
  29. Ward K. N., Gray J. J., Efstathiou S. Brief report: primary human herpesvirus 6 infection in a patient following liver transplantation from a seropositive donor. J Med Virol. 1989 Jun;28(2):69–72. doi: 10.1002/jmv.1890280203. [DOI] [PubMed] [Google Scholar]
  30. Wyatt L. S., Balachandran N., Frenkel N. Variations in the replication and antigenic properties of human herpesvirus 6 strains. J Infect Dis. 1990 Oct;162(4):852–857. doi: 10.1093/infdis/162.4.852. [DOI] [PubMed] [Google Scholar]
  31. Yamanishi K., Kondo T., Kondo K., Hayakawa Y., Kido S., Takahashi K., Takahashi M. Exanthem subitum and human herpesvirus 6 (HHV-6) infection. Adv Exp Med Biol. 1990;278:29–37. doi: 10.1007/978-1-4684-5853-4_4. [DOI] [PubMed] [Google Scholar]
  32. Yamanishi K., Okuno T., Shiraki K., Takahashi M., Kondo T., Asano Y., Kurata T. Identification of human herpesvirus-6 as a causal agent for exanthem subitum. Lancet. 1988 May 14;1(8594):1065–1067. doi: 10.1016/s0140-6736(88)91893-4. [DOI] [PubMed] [Google Scholar]

Articles from Proceedings of the National Academy of Sciences of the United States of America are provided here courtesy of National Academy of Sciences

RESOURCES