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. 1974 May;13(5):1037–1045. doi: 10.1128/jvi.13.5.1037-1045.1974

Analysis of a Viral Agent Isolated from Multiple Sclerosis Brain Tissue: Characterization as a Parainfluenzavirus Type 1

L J Lewandowski a, F S Lief a, M A Verini a,1, M M Pienkowski a,2, V ter Meulen a,3, H Koprowski a
PMCID: PMC355412  PMID: 4363249

Abstract

A virus originally isolated from cell cultures obtained by lysolecithin-induced fusion of human multiple sclerosis brain cells with CV-1 cells has been analyzed for its antigenic, RNA, and polypeptide compositions, and for selective biological properties. Our findings establish that this isolate, designated 6/94 virus, contains a 50S RNA genome and is, as yet, indistinguishable from Sendai virus in its antigenic and total polypeptide compositions. Despite these similarities, the 6/94 and Sendai viruses differ in certain phenotypic properties. 6/94 virus is markedly less cytocidal for chick fibroblasts, especially at 37 C and, after β-propiolactone inactivation, it possesses a greater capacity for cell fusion and a lower toxicity than does comparably treated Sendai virus. In addition, 6/94 virus shows greater hemolytic activity.

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Selected References

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  1. Apostolov K., Almeida J. D. Interaction of Sendai (HVJ) virus with human erythrocytes: a morphological study of haemolysis cell fusion. J Gen Virol. 1972 Jun;15(3):227–234. doi: 10.1099/0022-1317-15-3-227. [DOI] [PubMed] [Google Scholar]
  2. Barry R. D., Bukrinskaya A. G. The nucleic acid of Sendai virus and ribonucleic acid synthesis in cells infected by Sendai virus. J Gen Virol. 1968 Jan;2(1):71–79. doi: 10.1099/0022-1317-2-1-71. [DOI] [PubMed] [Google Scholar]
  3. Blair C. D., Duesberg P. H. Myxovirus ribonucleic acids. Annu Rev Microbiol. 1970;24:539–574. doi: 10.1146/annurev.mi.24.100170.002543. [DOI] [PubMed] [Google Scholar]
  4. Blair C. D., Robinson W. S. Replication of Sendai virus. I. Comparison of the viral RNA and virus-specific RNA synthesis with Newcastle disease virus. Virology. 1968 Aug;35(4):537–549. doi: 10.1016/0042-6822(68)90284-5. [DOI] [PubMed] [Google Scholar]
  5. Content J., Duesberg P. H. Electrophoretic distribution of the proteins and glycoproteins of influenza virus and Sendai virus. J Virol. 1970 Dec;6(6):707–716. doi: 10.1128/jvi.6.6.707-716.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Croce C. M., Koprowski H., Eagle H. Effect of environmental pH on the efficiency of cellular hybridization. Proc Natl Acad Sci U S A. 1972 Jul;69(7):1953–1956. doi: 10.1073/pnas.69.7.1953. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Dubois-Dalcq M., Schumacher G., Sever J. L. Acute multiple sclerosis: electron-microscopic evidence for and against a viral agent in the plaques. Lancet. 1973 Dec 22;2(7843):1408–1411. doi: 10.1016/s0140-6736(73)92801-8. [DOI] [PubMed] [Google Scholar]
  8. Gavrilov V. I., Asher D. M., Vyalushkina S. D., Ratushkina L. S., Zmieva R. G., Tumyan B. G. Persistent infection of continuous line of pig kidney cells with a variant of the WSN strain of influenza A 0 virus. Proc Soc Exp Biol Med. 1972 May;140(1):109–117. doi: 10.3181/00379727-140-36405. [DOI] [PubMed] [Google Scholar]
  9. Haspel M. V., Knight P. R., Duff R. G., Rapp F. Activation of a latent measles virus infection in hamster cells. J Virol. 1973 Oct;12(4):690–695. doi: 10.1128/jvi.12.4.690-695.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Howe C., Morgan C. Interactions between Sendai virus and human erythrocytes. J Virol. 1969 Jan;3(1):70–81. doi: 10.1128/jvi.3.1.70-81.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Iwasaki Y., Koprowski H., Müller D., ter Meulen V., Käckell Y. M. Morphogenesis and structure of a virus in cells cultured from brain tissue from two cases of multiple sclerosis. Lab Invest. 1973 Apr;28(4):494–500. [PubMed] [Google Scholar]
  12. Kelloff G., Vogt P. K. Localization of avian tumor virus group-specific antigen in cell and virus. Virology. 1966 Jul;29(3):377–384. doi: 10.1016/0042-6822(66)90213-3. [DOI] [PubMed] [Google Scholar]
  13. Kingsbury D. W., Portner A., Darlington R. W. Properties of incomplete Sendai virions and subgenomic viral RNAs. Virology. 1970 Dec;42(4):857–871. doi: 10.1016/0042-6822(70)90335-1. [DOI] [PubMed] [Google Scholar]
  14. Kingsbury D. W., Portner A. On the genesis of incomplete Sendai virions. Virology. 1970 Dec;42(4):872–879. doi: 10.1016/0042-6822(70)90336-3. [DOI] [PubMed] [Google Scholar]
  15. Kolakofsky D., Spahr P. F., Koprowski H. Comparison of 6-94 virus and Sendai virus RNA by RNA-RNA hybridization. J Virol. 1974 Apr;13(4):935–936. doi: 10.1128/jvi.13.4.935-936.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  17. Lewandowski L. J., Content J., Leppla S. H. Characterization of the subunit structure of the ribonucleic acid genome of influenza virus. J Virol. 1971 Nov;8(5):701–707. doi: 10.1128/jvi.8.5.701-707.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Lewandowski L. J., Traynor B. L. Comparison of the structure and polypeptide composition of three double-stranded ribonucleic acid-containing viruses (diplornaviruses): cytoplasmic polyhedrosis virus, wound tumor virus, and reovirus. J Virol. 1972 Nov;10(5):1053–1070. doi: 10.1128/jvi.10.5.1053-1070.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Nagata I., Kimura Y., Ito Y., Tanaka T. Temperature-sensitive phenomenon of viral maturation observed in BHK cells persistently infected with HVJ. Virology. 1972 Aug;49(2):453–461. doi: 10.1016/0042-6822(72)90497-7. [DOI] [PubMed] [Google Scholar]
  20. Narang H. K., Field E. J. Paramyxovirus like tubules in multiple sclerosis biopsy material. Acta Neuropathol. 1973;25(4):281–290. doi: 10.1007/BF00691756. [DOI] [PubMed] [Google Scholar]
  21. Oyanagi S., Rorke L. B., Katz M., Koprowski H. Histopathology and electron microscopy of three cases of subacute sclerosing panencephalitis (SSPE). Acta Neuropathol. 1971;18(1):58–73. doi: 10.1007/BF00684475. [DOI] [PubMed] [Google Scholar]
  22. Preble O. T., Youngner J. S. Selection of temperature-sensitive mutants during persistent infection: role in maintenance of persistent Newcastle disease virus infections of L cells. J Virol. 1973 Sep;12(3):481–491. doi: 10.1128/jvi.12.3.481-491.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Preble O. T., Youngner J. S. Temperature-sensitive defect of mutants isolated from L cells persistently infected with Newcastle disease virus. J Virol. 1973 Sep;12(3):472–480. doi: 10.1128/jvi.12.3.472-480.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Preble O. T., Youngner J. S. Temperature-sensitive mutants isolated from L cells persistently infected with Newcastle disease virus. J Virol. 1972 Feb;9(2):200–206. doi: 10.1128/jvi.9.2.200-206.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Prineas J. Paramyxovirus-like particles associated with acute demyelination in chronic relapsing multiple sclerosis. Science. 1972 Nov 17;178(4062):760–763. doi: 10.1126/science.178.4062.760. [DOI] [PubMed] [Google Scholar]
  26. Raine C. S., Powers J. M., Suzuki K. Acute multiple sclerosis. Confirmation of "paramyxovirus-like" intranuclear inclusions. Arch Neurol. 1974 Jan;30(1):39–46. doi: 10.1001/archneur.1974.00490310041007. [DOI] [PubMed] [Google Scholar]
  27. Schwöbel W., Ahl R. Peristence of sindbis virus in BHK-21 cell cultures. Arch Gesamte Virusforsch. 1972;38(1):1–10. doi: 10.1007/BF01241350. [DOI] [PubMed] [Google Scholar]
  28. Simizu B., Takayama N. Isolation of two plaque mutants of Western equine encephalitis virus differing in virulence for mice. J Virol. 1969 Nov;4(5):799–800. doi: 10.1128/jvi.4.5.799-800.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. TAKEMOTO K. K., HABEL K. Virus-cell relationship in a carrier culture of HeLa cells and Coxsackie A9 virus. Virology. 1959 Jan;7(1):28–44. doi: 10.1016/0042-6822(59)90175-8. [DOI] [PubMed] [Google Scholar]
  30. Thacore H., Youngner J. S. Cells persistently infected with newcastle disease virus: I. Properties of mutants isolated from persistently infected L cells. J Virol. 1969 Sep;4(3):244–251. doi: 10.1128/jvi.4.3.244-251.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Watanabe I., Okazaki H. Virus-like structure in multiple sclerosis. Lancet. 1973 Sep 8;2(7828):569–570. doi: 10.1016/s0140-6736(73)92394-5. [DOI] [PubMed] [Google Scholar]

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