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. 1979 Mar;23(3):775–786. doi: 10.1128/iai.23.3.775-786.1979

Variable infection of Vero cells and homologous interference after co-cultivation with HeLa cells with persistent defective infection by Edmonston measles virus.

R Rustigian, S H Winston, R W Darlington
PMCID: PMC414233  PMID: 457258

Abstract

The HeLa subline K11A-HG-1 (line of HeLa cells persistently infected with Edomonston measles virus but containing little or no transmissible infectious virus) was co-cultivated with Vero cells. Focal syncytia were formed containing measles antigen and accumulations of nucleocapsid-like structures with no detectable production of transmissible infectious virus or positive hemadsorption. The infection aborted between 2 and 3 weeks after preparation of co-cultures. Upon subculture of co-cultures, occasionally complete infections (progressive syncytial degeneration, hemadsorption, and production of transmissible infectious virus) appeared. A linear dose response curve for nontransmissible infection was obtained along with evidence that measles antigen had to be present on the surface of K11A-HG-1 cells for their infectivity for Vero cells. The basis for initiation of Vero cell infection by living K11A-HG-1 cells, but not by nonviable intact K11A-HG-1 cells killed by a virus-preserving technique, nor by disrupted K11A-HG-1 cells, is, at present, a matter of speculation. However, several lines of evidence were obtained which suggested that subsequent development of delayed variable transmissible Vero cell infection occurred because of a type of viral interference, including the presence of an inhibitor in K11A-HG-1 cultures, the bulk of which was cell-associated.

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Selected References

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  1. Barbanti-Brodano G., Oyanagi S., Katz M., Koprowski H. Presence of 2 different viral agents in brain cells of patients with subacute sclerosing panencephalitis. Proc Soc Exp Biol Med. 1970 May;134(1):230–236. doi: 10.3181/00379727-134-34765. [DOI] [PubMed] [Google Scholar]
  2. Baublis J. V., Payne F. E. Measles antigen and syncytium formtion in brain cell cultures from subacute sclerosing panencephalitis (SSPE). Proc Soc Exp Biol Med. 1968 Nov;129(2):593–597. doi: 10.3181/00379727-129-33377. [DOI] [PubMed] [Google Scholar]
  3. Billiau A., Sobis H., De Somer P. Influence of interferon on virus particle formation in different oncornavirus carrier cell lines. Int J Cancer. 1973 Nov 15;12(3):646–653. doi: 10.1002/ijc.2910120313. [DOI] [PubMed] [Google Scholar]
  4. Burnstein T., Jacobsen L. B., Zeman W., Chen T. T. Persistent infection of BSC-1 cells by defective measles virus derived from subacute sclerosing panencephalitis. Infect Immun. 1974 Dec;10(6):1378–1382. doi: 10.1128/iai.10.6.1378-1382.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Darlington R. W., Portner A., Kingsbury D. W. Sendai virus replication: an ultrastructural comparison of productive and abortive infections in avian cells. J Gen Virol. 1970 Dec;9(3):169–177. doi: 10.1099/0022-1317-9-3-169. [DOI] [PubMed] [Google Scholar]
  6. Doi Y., Sanpe T., Nakajima M., Okawa S., Koto T. Properties of a cytopathic agent isolated from a patient with subacute sclerosing panencephalitis in Japan. Jpn J Med Sci Biol. 1972 Oct;25(5):321–333. doi: 10.7883/yoken1952.25.321. [DOI] [PubMed] [Google Scholar]
  7. Friedman R. M., Ramseur J. M. Inhibition of murine leukemia virus production in chronically infected AKR cells: a novel effect of interferon. Proc Natl Acad Sci U S A. 1974 Sep;71(9):3542–3544. doi: 10.1073/pnas.71.9.3542. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Guggenheim M. A., Tyrrell S., Rabson A. S. Studies on Sendai virus cell fusion factor. Proc Soc Exp Biol Med. 1968 Dec;129(3):854–857. doi: 10.3181/00379727-129-33441. [DOI] [PubMed] [Google Scholar]
  9. Horta-Barbosa L., Fuccillo D. A., London W. T., Jabbour J. T., Zeman W., Sever J. L. Isolation of measles virus from brain cell cultures of two patients with subacute sclerosing panencephalitis. Proc Soc Exp Biol Med. 1969 Oct;132(1):272–277. doi: 10.3181/00379727-132-34196. [DOI] [PubMed] [Google Scholar]
  10. Huang A. S. Defective interfering viruses. Annu Rev Microbiol. 1973;27:101–117. doi: 10.1146/annurev.mi.27.100173.000533. [DOI] [PubMed] [Google Scholar]
  11. ISAACS A. Particle counts and infectivity titrations for animal viruses. Adv Virus Res. 1957;4:111–158. doi: 10.1016/s0065-3527(08)60597-7. [DOI] [PubMed] [Google Scholar]
  12. Johnson R. T., Gibbs C. J. Editorial: Koch's postulates and slow infections of the nervous system. Arch Neurol. 1974 Jan;30(1):36–38. doi: 10.1001/archneur.1974.00490310038006. [DOI] [PubMed] [Google Scholar]
  13. Kettyls G. D., Dunn H. G., Dombsky N., Turnbull I. M. Subacute sclerosing panencephalitis: isolation of a measles-like virus in tissue culture of brain biopsy. Can Med Assoc J. 1970 Nov 21;103(11):1183–1184. [PMC free article] [PubMed] [Google Scholar]
  14. Kratzsch V., Hall W. W., Nagashima K., ter Meulen V. Biological and biochemical characterization of a latent subacute sclerosing panencephalitis (SSPE) virus infection in tissue culture. J Med Virol. 1977;1(2):139–154. doi: 10.1002/jmv.1890010207. [DOI] [PubMed] [Google Scholar]
  15. Menna J. H., Collins A. R., Flanagan T. D. Characterization of an in vitro persistent-state measles virus infection: establishment and virological characterization of the BGM/MV cell line. Infect Immun. 1975 Jan;11(1):152–158. doi: 10.1128/iai.11.1.152-158.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Menna J. H., Collins A. R., Flanagan T. D. Characterization of an in vitro persistent-state measles virus infection: species characterization and interference in the BGM/MV cell line. Infect Immun. 1975 Jan;11(1):159–163. doi: 10.1128/iai.11.1.159-163.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Modlin J. F., Jabbour J. T., Witte J. J., Halsey N. A. Epidemiologic studies of measles, measles vaccine, and subacute sclerosing panencephalitis. Pediatrics. 1977 Apr;59(4):505–512. [PubMed] [Google Scholar]
  18. Nakai M., Imagawa D. T. Electron microscopy of measles virus replication. J Virol. 1969 Feb;3(2):187–197. doi: 10.1128/jvi.3.2.187-197.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Nishiyama Y. Studies of L cells persistently infected with VSV: factors involved in the regulation of persistent infection. J Gen Virol. 1977 May;35(2):265–279. doi: 10.1099/0022-1317-35-2-265. [DOI] [PubMed] [Google Scholar]
  20. Norrby E. C., Magnusson P. Some morphological characteristics of the internal component of measles virus. Arch Gesamte Virusforsch. 1965;17(3):443–447. doi: 10.1007/BF01241199. [DOI] [PubMed] [Google Scholar]
  21. Payne F. E., Baublis J. V., Itabashi H. H. Isolation of measles virus from cell cultures of brain from a patient with subacute sclerosing panencephalitis. N Engl J Med. 1969 Sep 11;281(11):585–589. doi: 10.1056/NEJM196909112811103. [DOI] [PubMed] [Google Scholar]
  22. Pitha P. M., Rowe W. P., Oxman M. N. Effect of interferon on exogenous, endogenous, and chroniv murine leukemia virus infection. Virology. 1976 Apr;70(2):324–338. doi: 10.1016/0042-6822(76)90275-0. [DOI] [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 viruses and the etiology of chronic and inapparent infections. J Infect Dis. 1975 Apr;131(4):467–473. doi: 10.1093/infdis/131.4.467. [DOI] [PubMed] [Google Scholar]
  25. RUSTIGIAN R. A carrier state in HeLa cells with measles virus (Edmonston strain) apparently associated with non-infectious virus. Virology. 1962 Jan;16:101–104. doi: 10.1016/0042-6822(62)90212-x. [DOI] [PubMed] [Google Scholar]
  26. Rima B. K., Davidson W. B., Martin S. J. The role of defective interfering particles in persistent infection of Vero cells by measles virus. J Gen Virol. 1977 Apr;35(1):89–97. doi: 10.1099/0022-1317-35-1-89. [DOI] [PubMed] [Google Scholar]
  27. Rima R. K., Martin S. J. Persistent infection of tissue culture cells by RNA viruses. Med Microbiol Immunol. 1976 Jun 1;162(2):89–119. doi: 10.1007/BF02121320. [DOI] [PubMed] [Google Scholar]
  28. Rustigian R. Persistent infection of cells in culture by measles virus. I. Development and characteristics of HeLa sublines persistently infected with complete virus. J Bacteriol. 1966 Dec;92(6):1792–1804. doi: 10.1128/jb.92.6.1792-1804.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Rustigian R. Persistent infection of cells in culture by measles virus. II. Effect of measles antibody on persistently infected HeLa sublines and recovery of a HeLa clonal line persistently infected with incomplete virus. J Bacteriol. 1966 Dec;92(6):1805–1811. doi: 10.1128/jb.92.6.1805-1811.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Shirodaria P. V., Dermott E., Gould E. A. Some characteristics of salt-dependent haemagglutinating measles viruses. J Gen Virol. 1976 Oct;33(1):107–115. doi: 10.1099/0022-1317-33-1-107. [DOI] [PubMed] [Google Scholar]
  31. Tyrrell D. L., Norrby E. Structural polypeptides of measles virus. J Gen Virol. 1978 May;39(2):219–229. doi: 10.1099/0022-1317-39-2-219. [DOI] [PubMed] [Google Scholar]
  32. Ueda S., Okuno Y., Hamamoto Y., Oya H. Subacute sclerosing panencephalitis (SSPE): isolation of a defective variant of measles virus from brain obtained at autopsy. Biken J. 1975 Jun;18(2):113–122. [PubMed] [Google Scholar]
  33. WATERSON A. P., CRUICKSHANK J. G., LAURENCE G. D., KANAREK A. D. The nature of measles virus. Virology. 1961 Nov;15:379–382. doi: 10.1016/0042-6822(61)90370-1. [DOI] [PubMed] [Google Scholar]
  34. Zylber E., Vesco C., Penman S. Selective inhibition of the synthesis of mitochondria-associated RNA by ethidium bromide. J Mol Biol. 1969 Aug 28;44(1):195–204. doi: 10.1016/0022-2836(69)90414-8. [DOI] [PubMed] [Google Scholar]

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