Skip to main content
Elsevier - PMC COVID-19 Collection logoLink to Elsevier - PMC COVID-19 Collection
. 2002 Nov 12;1(7):585–595. doi: 10.1016/0168-1702(84)90015-7

Measles virus gene expression in subacute sclerosing panencephalitis

Knut Baczko 1, Micheal J Carter 1,, Martin Billeter 1,∗∗, Volker ter Meulen 1
PMCID: PMC7134159  PMID: 6534032

Abstract

RNA was extracted from the diseased brain of a case of human subacute sclerosing panencephalitis (SSPE) and analysed for the expression of measles-specific RNA. Measles virus-specific mRNAs were present, but the amount of matrix (M) protein mRNA was greatly reduced in comparison to lytically infected cells and phospho- (P) protein mRNA was hardly detectable whereas the level of the corresponding intermediate-sized (is-) RNA was greatly increased. RNA obtained from the human brain was also translated in vitro and measles virus nucleocapsid and P protein was produced. However, in marked contrast to control reactions M protein was not detected in the products formed by translation in vitro. These results indicate an impaired measles virus M protein mRNA synthesis in infected brain tissue.

Keywords: measles, subacute sclerosing panencephalitis, transcription, translation, matrix protein

References

  1. Baczko K., Billeter M., ter Meulen V. Purification and molecular weight determination of measles virus genomic RNA. J. Gen. Virol. 1983;64:1409–1413. doi: 10.1099/0022-1317-64-6-1409. [DOI] [PubMed] [Google Scholar]
  2. Baczko K., Billeter M., ter Meulen V. Expression of measles virus RNA in brain tissue. In: Bishop D.H.L., Compans R.W., editors. The Replication of Negative Strand Viruses. Elsevier/North Holland; Amsterdam: 1984. (in press). [Google Scholar]
  3. Bailey J.M., Davidson N. Methylmercury as a reversible denaturing agent for agarose gel electrophoresis. Anal. Biochem. 1976;70:75–88. doi: 10.1016/s0003-2697(76)80049-8. [DOI] [PubMed] [Google Scholar]
  4. Bellini W.J., Silver G.D., McFarlin D.E. Biosynthesis of measles virus hemagglutinin in persistently infected cells. Arch. Virol. 1983;75:87–101. doi: 10.1007/BF01314129. [DOI] [PubMed] [Google Scholar]
  5. Bellini W.J., Englund G., Richardson C.D., Rozenblatt S. Positive identification of a measles virus cDNA clone encoding a region of the phosphoprotein. J. Virol. 1984;50:939–942. doi: 10.1128/jvi.50.3.939-942.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Billeter M., Baczko K., ter Meulen V. Cloning of DNA corresponding to four different measles virus genomic regions. Virology. 1984;132:149–159. doi: 10.1016/0042-6822(84)90099-0. [DOI] [PubMed] [Google Scholar]
  7. Carter M.J., Willcocks M.M., ter Meulen V. Defective translation of measles virus matrix protein in a subacute sclerosing Panencephalitis Cell Line. Nature. 1983;305:153–155. doi: 10.1038/305153a0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Carter M., Willcocks M.M., Löffler S., ter Meulen V. Comparison of lytic and persistent measles virus matrix proteins by competition radioimmunoassay. J. Gen. Virol. 1983;64:1801–1805. doi: 10.1099/0022-1317-64-8-1801. [DOI] [PubMed] [Google Scholar]
  9. Carter M.J., Willcocks M.M., ter Meulen V. Synthesis of matrix protein in a subacute sclerosing panencephalitis cell line. In: Bishop D.H.L., Compans R.W., editors. The Replication of Negative Strand Viruses. Elsevier/North Holland; Amsterdam: 1984. (in press). [Google Scholar]
  10. Chirgwin J.M., Przybyla A.E., MacDonald R.J., Rutter W.J. Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease. Biochem. 1979;18:5294–5299. doi: 10.1021/bi00591a005. [DOI] [PubMed] [Google Scholar]
  11. Collins P.L., Wertz G.W. Vol. 80. 1983. cDNA cloning and transcriptional mapping of nine polyadenylated RNAs encoded by the genome of human respiratory syncytial virus; pp. 3208–3212. (Proc. Natl. Acad. Sci. U.S.A.). [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Gilden D.H., Rorke L.B., Tanaka R. Acute SSPE. Arch. Neurol. 1975;32:644–646. doi: 10.1001/archneur.1975.00490510100013. [DOI] [PubMed] [Google Scholar]
  13. Gorecki M., Rozenblatt S. Vol. 77. 1980. Cloning of DNA complementary to the measles virus mRNA encoding nucleocapsid protein; pp. 3686–3690. (Proc. Natl. Acad. Sci. U.S.A.). [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Hall W.W., Choppin P.W. Evidence for the lack of synthesis of the M polypeptide of measles virus in brain cells from SSPE. Virology. 1979;99:443–447. doi: 10.1016/0042-6822(79)90026-6. [DOI] [PubMed] [Google Scholar]
  15. Hall W.W., Choppin P.W. Measles-virus proteins in the brain tissue of patients with subacute sclerosing panencephalitis. Absence of the M protein. New Engl. J. Med. 1981;304:1152–1155. doi: 10.1056/NEJM198105073041906. [DOI] [PubMed] [Google Scholar]
  16. Hall W.W., Lamb R.A., Choppin P.W. Vol. 76. 1979. Measles and subacute sclerosing panencephalitis virus proteins: lack of antibodies to the M protein in patients with subacute sclerosing panencephalitis; pp. 2047–2051. (Proc. Natl. Acad. Sci. U.S.A.). [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Herman R.C., Adler S., Lazzarini R.A., Colonno R.J., Banerjee A.K., Westphal H. Intervening polyadenylate sequences in RNA transcripts of vesicular stomatitis virus. Cell. 1978;15:587–596. doi: 10.1016/0092-8674(78)90027-2. [DOI] [PubMed] [Google Scholar]
  18. Holland J.J., Grabau E.A., Jones C.L., Sember B.L. Evolution of multiple genome mutations during long-term persistent infection by vesicular stomatitis virus. Cell. 1979;16:495–504. doi: 10.1016/0092-8674(79)90024-2. [DOI] [PubMed] [Google Scholar]
  19. Katz M., Koprowski H. The significance of failure to isolate infectious viruses in cases of subacute sclerosing panencephalitis. Arch. Ges. Virusforsch. 1973;41:390–393. doi: 10.1007/BF01250213. [DOI] [PubMed] [Google Scholar]
  20. Laemmli U.K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature (London) 1970;227:680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  21. Lin F.H., Thormar H. Absence of M protein in a cell-associated subacute sclerosing panencephalitis virus. Nature (London) 1980;285:490–492. doi: 10.1038/285490a0. [DOI] [PubMed] [Google Scholar]
  22. Machamer C.E., Hayes E.C., Zweerink H.J. Cells infected with a cell-associated subacute sclerosing panencephalitis virus do not express M protein. Virology. 1981;108:515–520. doi: 10.1016/0042-6822(81)90460-8. [DOI] [PubMed] [Google Scholar]
  23. Pelham H.R.B., Jackson R.J. An efficient mRNA-dependent translation system from reticulocyte lysates. Eur. J. Biochem. 1976;67:247–256. doi: 10.1111/j.1432-1033.1976.tb10656.x. [DOI] [PubMed] [Google Scholar]
  24. Rima B.K., Lappin S.A., Roberts M.W., Martin S.J. A study of phosphorylation of the measles membrane protein. J. Gen. Virol. 1981;56:447–450. doi: 10.1099/0022-1317-56-2-447. [DOI] [PubMed] [Google Scholar]
  25. Rozenblatt S., Gesang C., Lavie V., Neuman F. Cloning and characterization of DNA complementary to the measles virus mRNA encoding hemagglutinin and matrix protein. J. Virol. 1982;42:790–799. doi: 10.1128/jvi.42.3.790-797.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Siddell S.G., Wege H., ter Meulen V. The biology of Coronaviruses. J. Gen. Virol. 1983;64:761–776. doi: 10.1099/0022-1317-64-4-761. [DOI] [PubMed] [Google Scholar]
  27. Simons K., Garoff H. The budding mechanisms of enveloped animal viruses. J. Gen. Virol. 1980;50:1–21. doi: 10.1099/0022-1317-50-1-1. [DOI] [PubMed] [Google Scholar]
  28. Stephenson J.R., ter Meulen V. 1979. Antigenic relationships between measles and canine distemper viruses: comparison of the immune response in animals and humans to individual virus-specific polypeptides; pp. 6601–6605. (Proc. Natl. Acad. Sci. U.S.A.). [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Ter Meulen V., Stephenson J.R., Kreth H.W. Subacute sclerosing panencephalitis. In: Fraenkel-Conrat H., Wagner R.R., editors. Vol. 18. 1983. pp. 105–159. (Comprehensive Virology). [Google Scholar]
  30. Ter Meulen V., Carter M.J. Morbillivirus persistent infections in animals and man. In: Mahy B.W.J., Minson A.C., Darby G.K., editors. Virus Persistence. Cambridge University Press; Cambridge: 1982. pp. 97–132. [Google Scholar]
  31. Thomas P.S. Vol. 77. 1980. Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose; pp. 5201–5205. (Proc. Natl. Acad. Sci. U.S.A.). [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Wechsler S.L., Rustigian R., Stallcup K.C., Byers K.B., Winston S.H., Fields B.N. Measles virus-specific polypeptide synthesis in two persistently infected HeLa cell lines. J. Virol. 1979;31:677–684. doi: 10.1128/jvi.31.3.677-684.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Virus Research are provided here courtesy of Elsevier

RESOURCES