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. 1979 Dec;32(3):790–795. doi: 10.1128/jvi.32.3.790-795.1979

Stabilization of "A" particles of coxsackievirus B3 by a HeLa cell plasma membrane extract.

M L McGeady, R L Crowell
PMCID: PMC525926  PMID: 513203

Abstract

Previous studies in our laboratory showed that HeLa cell plasma membranes were recovered from sucrose gradients in two major bands and that the heavier band possessed a putative inhibitor of uncoating of coxsackievirus B3. It has now been found that the mechanism of inhibition is the stabilization of "A" particles against inactivation at 37 degrees C. [3H]uridine-labeled virions converted to A particles by band 4, the heavier band, were four times more stable at 37 degrees C than those produced by band 3. Partially purified A particles from both bands were equally unstable. It was found that the stabilizing factor was extractable by saline from band 4 and remained soluble after centrifugation (109,000 X g for 2 h). Addition to A particles of this soluble factor isolated from either band 4 or band 3 stabilized the A particles. The stabilizing factor could not be replaced by an extract from band 3 or by bovine serum albumin. Thus, the finding that the membrane factor inhibits virus uncoating by stabilizing A particles against spontaneous disruption at 37 degrees C focuses attention on an inherent problem associated with defining receptor-mediated virus uncoating.

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Selected References

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

  1. Bosmann H. B., Hagopian A., Eylar E. H. Cellular membranes: the isolation and characterization of the plasma and smooth membranes of HeLa cells. Arch Biochem Biophys. 1968 Oct;128(1):51–69. doi: 10.1016/0003-9861(68)90008-8. [DOI] [PubMed] [Google Scholar]
  2. CROWELL R. L., SYVERTON J. T. The mammalian cell-virus relationship. VI. Sustained infection of HeLa cells by Coxsackie B3 virus and effect on superinfection. J Exp Med. 1961 Feb 1;113:419–435. doi: 10.1084/jem.113.2.419. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Chan V. F., Black F. L. Uncoating of poliovirus by isolated plasma membranes. J Virol. 1970 Mar;5(3):309–312. doi: 10.1128/jvi.5.3.309-312.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Crowell R. L., Landau B. J., Philipson L. The early interaction of coxsackievirus B3 with HeLa cells. Proc Soc Exp Biol Med. 1971 Jul;137(3):1082–1088. doi: 10.3181/00379727-137-35732. [DOI] [PubMed] [Google Scholar]
  5. Crowell R. L., Philipson L. Specific alterations of coxsackievirus B3 eluted from HeLa cells. J Virol. 1971 Oct;8(4):509–515. doi: 10.1128/jvi.8.4.509-515.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. De Sena J., Mandel B. Studies on the in vitro uncoating of poliovirus. I. Characterization of the modifying factor and the modifying reaction. Virology. 1976 Apr;70(2):470–483. doi: 10.1016/0042-6822(76)90288-9. [DOI] [PubMed] [Google Scholar]
  7. De Sena J., Mandel B. Studies on the in vitro uncoating of poliovirus. II. Characteristics of the membrane-modified particle. Virology. 1977 May 15;78(2):554–566. doi: 10.1016/0042-6822(77)90130-1. [DOI] [PubMed] [Google Scholar]
  8. FENWICK M. L., COOPER P. D. Early interactions between poliovirus and ERK cells: some observations on the nature and significance of the rejected particles. Virology. 1962 Oct;18:212–223. doi: 10.1016/0042-6822(62)90007-7. [DOI] [PubMed] [Google Scholar]
  9. Fenwick M. L., Wall M. J. Factors determining the site of synthesis of poliovirus proteins: the early attachment of virus particles to endoplasmic membranes. J Cell Sci. 1973 Sep;13(2):403–413. doi: 10.1242/jcs.13.2.403. [DOI] [PubMed] [Google Scholar]
  10. Guttman N., Baltimore D. A plasma membrane component able to bind and alter virions of poliovirus type 1: studies on cell-free alteration using a simplified assay. Virology. 1977 Oct 1;82(1):25–36. doi: 10.1016/0042-6822(77)90029-0. [DOI] [PubMed] [Google Scholar]
  11. HOLLAND J. J., HOYER B. H. Early stages of enterovirus infection. Cold Spring Harb Symp Quant Biol. 1962;27:101–112. doi: 10.1101/sqb.1962.027.001.013. [DOI] [PubMed] [Google Scholar]
  12. HOLLAND J. J., McLAREN L. C., SYVERTON J. T. The mammalian cell-virus relationship. IV. Infection of naturally insusceptible cells with enterovirus ribonucleic acid. J Exp Med. 1959 Jul 1;110(1):65–80. doi: 10.1084/jem.110.1.65. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. JOKLIK W. K., DARNELL J. E., Jr The adsorption and early fate of purified poliovirus in HeLa cells. Virology. 1961 Apr;13:439–447. doi: 10.1016/0042-6822(61)90275-6. [DOI] [PubMed] [Google Scholar]
  14. Lonberg-Holm K., Gosser L. B., Shimshick E. J. Interaction of liposomes with subviral particles of poliovirus type 2 and rhinovirus type 2. J Virol. 1976 Aug;19(2):746–749. doi: 10.1128/jvi.19.2.746-749.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Lonberg-Holm K., Philipson L. Early interaction between animal viruses and cells. Monogr Virol. 1974;9:1–148. [PubMed] [Google Scholar]
  16. MANDEL B. THE FATE OF THE INOCULUM IN HELA CELLS INFECTED WITH POLIOVIRUS. Virology. 1965 Jan;25:152–154. doi: 10.1016/0042-6822(65)90264-3. [DOI] [PubMed] [Google Scholar]
  17. McGeady M. L., Siak J. S., Crowell R. L. Survival of coxsackievirus B3 under diverse environmental conditions. Appl Environ Microbiol. 1979 May;37(5):972–977. doi: 10.1128/aem.37.5.972-977.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Righthand V. F., Bagshaw J. C. Characterization of a regulator of host cell permissiveness to a specific enterovirus. Virology. 1978 May 1;86(1):148–156. doi: 10.1016/0042-6822(78)90015-6. [DOI] [PubMed] [Google Scholar]
  19. Roesing T. G., Toselli P. A., Crowell R. L. Elution and uncoating of Coxsackievirus B3 by isolated HeLa cell plasma membranes. J Virol. 1975 Mar;15(3):654–657. doi: 10.1128/jvi.15.3.654-657.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. WALLIS C., MENICK J. L. Cationic stabilization--a new property of enteroviruses. Virology. 1962 Apr;16:504–506. doi: 10.1016/0042-6822(62)90234-9. [DOI] [PubMed] [Google Scholar]

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