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. 1958 May 25;4(3):301–308. doi: 10.1083/jcb.4.3.301

Fine Structure of Changes Produced in Cultured Cells Sampled at Specified Intervals During a Single Growth Cycle of Polio Virus

Frances Kallman 1, Robley C Williams 1, Renato Dulbecco 1, Marguerite Vogt 1
PMCID: PMC2224474  PMID: 13549502

Abstract

Primary suspended cultures of rhesus monkey kidney cells were infected with poliomyelitis virus, type 1 (Brunhilde strain). The release of virus from these cells over a one-step growth curve was correlated with their change in fine structure, as seen in the electron microscope. Most of the cells were infected nearly simultaneously, and morphological changes developed in the cells were sufficiently synchronous to be classified into three stages. The earliest change (stage I) became visible at a time when virus release into the culture fluid begins, some 3 hours after adsorption. Accentuation of the abnormal characteristics soon occurs, at 4 to 7 hours after adsorption, and results in stage II. Stage III represents the appearance of cells after their rate of virus release had passed its maximum, and probably the abnormal morphology of these cells reflects non-specific physiological damage. There seems to be consistency between the previously described cellular changes as seen under the light microscope and the finer scale changes reported here. Cytoplasmic bodies, called U bodies, were seen in large number at the time when the virus release was the most rapid (stage II). While these bodies are not of proper size to be considered polio virus, they seem to be specifically related to the infection. No evidence was found for the presence of particles that could even be presumptively identified with those of polio virus.

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Selected References

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

  1. BARSKI G., ROBINEAUX R., ENDO M. Evolution of the cellular lesion induced by poliomyelitis virus in vitro as studied with phase contrast microcinematography. Ann N Y Acad Sci. 1955 Sep 27;61(4):899–901. doi: 10.1111/j.1749-6632.1955.tb42548.x. [DOI] [PubMed] [Google Scholar]
  2. CLARK S. L., Jr Cellular differentiation in the kidneys of newborn mice studies with the electron microscope. J Biophys Biochem Cytol. 1957 May 25;3(3):349–362. doi: 10.1083/jcb.3.3.349. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. DULBECCO R., VOGT M. Biological properties of poliomyelitis viruses as studied by the plaque technique. Ann N Y Acad Sci. 1955 Sep 27;61(4):790–800. doi: 10.1111/j.1749-6632.1955.tb42535.x. [DOI] [PubMed] [Google Scholar]
  4. DUNNEBACKE T. H. Correlation of the stage of cytopathic change with the release of poliomyelitis virus. Virology. 1956 Jun;2(3):399–410. doi: 10.1016/0042-6822(56)90034-4. [DOI] [PubMed] [Google Scholar]
  5. DUNNEBACKE T. H. Cytopathic changes associated with poliomyelitis infections in human amnion cells. Virology. 1956 Dec;2(6):811–819. doi: 10.1016/0042-6822(56)90060-5. [DOI] [PubMed] [Google Scholar]
  6. HARDING C. V., HARDING D., MCLIMANS W. F., RAKE G. Cytological changes accompanying the growth of poliomyelitis virus in cells of human origin (strain HeLa). Virology. 1956 Feb;2(1):109–125. doi: 10.1016/0042-6822(56)90080-0. [DOI] [PubMed] [Google Scholar]
  7. HOWES D. W., MELNICK J. L., REISSIG M. Sequence of morphological changes in epithelial cell cultures infected with poliovirus. J Exp Med. 1956 Sep 1;104(3):289–304. doi: 10.1084/jem.104.3.289. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. LWOFF A., DULBECCO R., VOGT M., LWOFF M. Kinetics of the release of poliomyelitis virus from single cells. Ann N Y Acad Sci. 1955 Sep 27;61(4):801–805. doi: 10.1111/j.1749-6632.1955.tb42536.x. [DOI] [PubMed] [Google Scholar]
  9. ROBBINS F. C., ENDERS J. F., WELLER T. H. Cytopathogenic effect of poliomyelitis viruses in vitro on, human embryonic tissues. Proc Soc Exp Biol Med. 1950 Nov;75(2):370–374. doi: 10.3181/00379727-75-18202. [DOI] [PubMed] [Google Scholar]
  10. RUSKA H., STUART D. C., Jr, WINSSER J. Electron microscopic visualization of intranuclear virus-like bodies in epithelial cells infected with poliomyelitis virus. Arch Gesamte Virusforsch. 1956;6(5):379–387. doi: 10.1007/BF01245924. [DOI] [PubMed] [Google Scholar]
  11. SCHWERDT C. E., FOGH J. The ratio of physical particles per infectious unit observed for poliomyelitis viruses. Virology. 1957 Aug;4(1):41–52. doi: 10.1016/0042-6822(57)90042-9. [DOI] [PubMed] [Google Scholar]

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