Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1962 Apr;83(4):837–843. doi: 10.1128/jb.83.4.837-843.1962

COMPARATIVE STUDIES OF THE MULTIPLICATION OF ANTIGENICALLY RELATED POXVIRUSES ON THE CHORIOALLANTOIC MEMBRANE OF THE CHICK EMBRYO

Nicholas Hahon 1, James J Friel 1
PMCID: PMC279364  PMID: 13903692

Abstract

Hahon, Nicholas (U. S. Army Chemical Corps, Frederick, Md.) and James J. Friel. Comparative studies of the multiplication of antigenically related poxviruses on the chorioallantoic membrane of the chick embryo. J. Bacteriol. 83:837–843. 1962.—A comparison was made of the general growth curves of several poxviruses, variola, alastrim, vaccinia, cowpox, rabbitpox, and monkeypox, on the chorioallantoic membrane of the chick embryo. All curves showed a lag period, followed by a tenfold increase of infectivity each 5 hr for approximately 20 to 25 hr, a peak growth level at 48 to 52 hr (except monkeypox), and a gradual decline after 72 hr.

Closer examination of the lag period revealed a rapid decline of virus infectivity within 2 to 4 hr after inoculation and the manifestation of an eclipse phase for 4 and 6 hr with all poxviruses. The lag period was terminated with the detection of intracellular virus at 8 to 12 hr, followed by the appearance of extracellular virus 2 to 6 hr later. The proportion of extracellular to intracellular virus was 0.1 or less throughout the different stages of poxvirus growth. In contrast to findings with the other poxviruses, however, extracellular virus equaled or exceeded the quantity of intracellular virus during the latter stages of the growth curves of variola and alastrim viruses.

Full text

PDF
837

Selected References

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

  1. ANDERSON S. G. The growth curve of vaccinia virus on the chorioallantois. Aust J Exp Biol Med Sci. 1954 Oct;32(5):633–639. doi: 10.1038/icb.1954.66. [DOI] [PubMed] [Google Scholar]
  2. DE FAZEKAS S. T., GROTH S., REID A. F. The neutralization of animal viruses. II. A critical comparison of hypotheses. J Immunol. 1958 Mar;80(3):225–235. [PubMed] [Google Scholar]
  3. DE FAZEKAS S. T., GROTH S., WATSON G. S., REID A. F. The neutralization of animal viruses. I. A model of virus-antibody interaction. J Immunol. 1958 Mar;80(3):215–224. [PubMed] [Google Scholar]
  4. DOWNIE A. W., HADDOCK D. W. A variant of cowpox virus. Lancet. 1952 May 24;1(6717):1049–1050. doi: 10.1016/s0140-6736(52)90698-3. [DOI] [PubMed] [Google Scholar]
  5. DULBECCO R., VOGT M., STRICKLAND A. G. A study of the basic aspects of neutralization of two animal viruses, western equine encephalitis virus and poliomyelitis virus. Virology. 1956 Apr;2(2):162–205. doi: 10.1016/0042-6822(56)90017-4. [DOI] [PubMed] [Google Scholar]
  6. FURNESS G., YOUNGNER J. S. One-step growth curves for vaccinia virus in cultures of monkey kidney cells. Virology. 1959 Nov;9:386–395. doi: 10.1016/0042-6822(59)90130-8. [DOI] [PubMed] [Google Scholar]
  7. HAHON N., LOUIE R., RATNER M. Method of chorioallantoic membrane inoculation which decreases nonspecific lesions. Proc Soc Exp Biol Med. 1957 Apr;94(4):697–700. doi: 10.3181/00379727-94-23056. [DOI] [PubMed] [Google Scholar]
  8. HAHON N., RATNER M., KOZIKOWSKI E. Factors influencing variola virus growth on the chorioallantoic membrane of embryonated eggs. J Bacteriol. 1958 Jun;75(6):707–712. doi: 10.1128/jb.75.6.707-712.1958. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. HOYLE L., FRISCH-NIGGEMEYER W. The disintegration of influenza virus particles on entry into the host cell; studies with virus labelled with radiophosphorus. J Hyg (Lond) 1955 Dec;53(4):474–486. doi: 10.1017/s0022172400000978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. OVERMAN J. R., TAMM I. Multiplication of vaccinia virus in the chorioallantoic membrane in vitro. Virology. 1957 Feb;3(1):173–184. doi: 10.1016/0042-6822(57)90031-4. [DOI] [PubMed] [Google Scholar]
  11. POSTLETHWAITE R. A plaque technique for the titration of vaccinia virus in chick embryo cells and some features of vaccinial infection in this system. Virology. 1960 Apr;10:466–482. doi: 10.1016/0042-6822(60)90130-6. [DOI] [PubMed] [Google Scholar]
  12. POSTLETHWAITE R., MAITLAND H. B. The eclipse phase of vaccinia virus growing in chick embryo cell monolayers and some technical procedures which affect its demonstration. J Hyg (Lond) 1960 Jun;58:133–145. doi: 10.1017/s0022172400038213. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. ROBINOW C. F. A note on stalked forms of viruses. J Gen Microbiol. 1950 May;4(2):242–243. doi: 10.1099/00221287-4-2-242. [DOI] [PubMed] [Google Scholar]
  14. RYDEN F. W., RANDALL C. C. The growth cycle of vaccinia in HeLa cells correlated with concurrent cellular changes. Am J Pathol. 1957 May-Jun;33(3):367–383. [PMC free article] [PubMed] [Google Scholar]
  15. SHOPE R. E. Report of Committee on Infectious Ectromelia of Mice (mouse pox). J Natl Cancer Inst. 1954 Oct;15(2):405–408. [PubMed] [Google Scholar]
  16. SMITH K. O., SHARP D. G. Interaction of virus with cells in tissue cultures. I. Adsorption on and growth of vaccinia virus in L cells. Virology. 1960 Jul;11:519–532. doi: 10.1016/0042-6822(60)90097-0. [DOI] [PubMed] [Google Scholar]
  17. YOSHINO K., TANIGUCHI H., TANIGUCHI S. Demonstration of the eclipse phase of herpes simplex virus by a new deembryonation technique. Virology. 1960 Jan;10:97–111. doi: 10.1016/0042-6822(60)90009-x. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Bacteriology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES