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. 1955 Sep 30;102(4):441–473. doi: 10.1084/jem.102.4.441

REPRODUCTION OF INFLUENZA VIRUSES

QUANTITATIVE INVESTIGATIONS WITH PARTICLE ENUMERATION PROCEDURES ON THE DYNAMICS OF INFLUENZA A AND B VIRUS REPRODUCTION

Frank L Horsfall Jr 1
PMCID: PMC2136520  PMID: 13263486

Abstract

Influenza A and B virus reproduction in the allantoic membrane of the intact chicken embryo was studied quantitatively with particle enumeration procedures. Virus particles were enumerated on the basis of two independent properties; capacity to infect and to cause hemagglutination. The infective property of influenza B virus (Lee) was even more unstable than that of influenza A virus (PR8). Inactivation occurred at a constant logarithmic rate which was independent of the concentration of particles and corresponded with first order reaction kinetics. In allantoic fluid at 35°C. either in vitro or in vivo, Lee virus had a half-life for infectivity of only 85 minutes. In contrast, the hemagglutinating property, like that of PR8, was relatively stable and was not appreciably affected by 12 hours at 35°C. On the basis that the number of non-infective particles is equal to the number of hemagglutinating particles minus the number of infective particles and that the number of cells lining the allnatoic membrane is 1.8 x 107, the effects of various particle-cell ratios on the reproductive process were analyzed. Adsorption of infective and non-infective Lee particles occurred at the same logarithmic rate, i.e. about 50 per cent in 72 minutes, and the rate was nearly independent of the particle-cell ratio up to a value of 55. The adsorption capacity of an allantoic cell was at least 44 Lee or 89 PR8 particles. The interval before new particles appeared in the allantoic fluid increased as the particle-cell ratio was decreased with both Lee and PR8. At ratios of 0.2 or less, the appearance time for infective particles was nearly identical to that for hemagglutinating particles with both viruses. At ratios of about 1.0, the "latent period" in the allantoic membrane per se was computed to be 150 to 160 minutes for both Lee and PR8. The number of particles, both infective and hemagglutinating, increased at a constant logarithmic rate for 6 hours or more after the adsorptive period. With Lee virus, at a particle-cell ratio of 5 or less, the doubling time was constant and had a value of 43 minutes. The dynamics of the logarithmic increase period suggest that reproduction corresponds to an autocatalytic reaction in which the rate is proportional to the amount of material produced. When the particle-cell ratio was increased to 10 or more, either with infective or non-infective (inactivated at 35°C. or 22°C.) particles, the doubling time increased to 65 minutes. Comparable effects from high ratios were found with PR8. Non-infective particles accumulated at a rapid rate after the interval of constant logarithmic increase regardless of the particle-cell ratio. This accumulation was even more striking with Lee than with PR8 as was expected because of the shorter half-life of the infective property. With both viruses at particle-cell ratios of 4 or more, a large proportion of the particles were non-infective within a few hours after new particles appeared. At particle-cell ratios of 0.2 or less, the maximal yield was relatively constant, i.e., about 900 to 1400 hemagglutinating particles per cell with Lee and 500 to 900 with PR8. However, even with very low ratios, i.e. 0.001 or less, it was not possible to obtain more than about 160 infective particles per cell with either virus regardless of the interval. As was expected, the lower the ratio, the longer was the interval before maximal yields were produced. At ratios of about 10, the maximal yield was reduced by 50 per cent or more with both viruses. Comparable reductions in yield were obtained whether the high particle-cell ratio was due to infective or non-infective (inactivated at 35°C. or 22°C.) particles. These findings indicate that there is a critical particle-cell ratio above which alterations appear in the dynamics of reproduction of influenza viruses. This ratio has a value of approximately 3. The observed alterations in the reproductive process are discussed in relation to the hypothesis that adsorption of 3 or more infective or non-infective particles per cell induces cell damage.

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Selected References

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  1. CAIRNS H. J. F., EDNEY M., FAZEKAS DE ST GROTH S. Quantitative aspects of influenza virus multiplication. J Immunol. 1952 Aug;69(2):155–181. [PubMed] [Google Scholar]
  2. CAIRNS H. J., MASON P. J. Production of influenza A virus in the cells of the allantois. J Immunol. 1953 Jul;71(1):38–40. [PubMed] [Google Scholar]
  3. DANIELS J. B., EATON M. D., PERRY M. E. Effect of glucose on the growth of influenza virus in deembryonated eggs and tissue cultures. J Immunol. 1952 Sep;69(3):321–329. [PubMed] [Google Scholar]
  4. FINTER N. B., LIU O. C., HENLE W. Studies on host-virus interactions in the chick embryo-influenza virus system. X. An experimental analysis of the von Magnus phenomenon. J Exp Med. 1955 May 1;101(5):461–478. doi: 10.1084/jem.101.5.461. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. GINSBERG H. S., HORSFALL F. L., Jr Characteristics of the multiplication cycle of pneumonia virus of mice (PVM). J Exp Med. 1951 Feb;93(2):151–160. doi: 10.1084/jem.93.2.151. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. GINSBERG H. S., HORSFALL F. L., Jr Quantitative aspects of the multiplication of influenza A virus in the mouse lung; relation between the degree of viral multiplication and the extent of pneumonia. J Exp Med. 1952 Feb;95(2):135–145. doi: 10.1084/jem.95.2.135. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. HENLE G., GIRARDI A., HENLE W. A non-transmissible cytopathogenic effect of influenza virus in tissue culture accompanied by formation of non-infectious hemagglutinins. J Exp Med. 1955 Jan 1;101(1):25–41. doi: 10.1084/jem.101.1.25. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. HENLE W., HENLE G. Studies on host-virus interactions in the chick embryo-influenza virus system; development of infectivity, hemagglutination, and complement fixation activities during the first infectious cycle. J Exp Med. 1949 Jul;90(1):23–37. doi: 10.1084/jem.90.1.23. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. HENLE W., LIU O. C. Studies on host-virus interactions in the chick embryo-influenza virus system. VI. Evidence for multiplicity reactivation of inactivated virus. J Exp Med. 1951 Oct;94(4):305–322. doi: 10.1084/jem.94.4.305. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. HENLE W. Studies on host-virus interactions in the chick embryo-influenza virus system; adsorption and recovery of seed virus. J Exp Med. 1949 Jul;90(1):1–11. doi: 10.1084/jem.90.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. HORSFALL F. L., Jr, GINSBERG H. S. An improved CO2 cabinet for low temperature storage of infectious agents with gaseous CO2 excluded from the specimen compartment. J Bacteriol. 1951 Apr;61(4):443–451. doi: 10.1128/jb.61.4.443-451.1951. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. HORSFALL F. L., Jr On the reproduction of influenza virus; quantitative studies with procedures which enumerate infective and hemagglutinating virus particles. J Exp Med. 1954 Aug 1;100(2):135–161. doi: 10.1084/jem.100.2.135. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Henle G., Henle W. STUDIES ON THE TOXICITY OF INFLUENZA VIRUSES : I. THE EFFECT OF INTRACEREBRAL INJECTION OF INFLUENZA VIRUSES. J Exp Med. 1946 Nov 30;84(6):623–637. doi: 10.1084/jem.84.6.623. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Henle W., Henle G. STUDIES ON THE TOXICITY OF INFLUENZA VIRUSES : II. THE EFFECT OF INTRA-ABDOMINAL AND INTRAVENOUS INJECTION OF INFLUENZA VIRUSES. J Exp Med. 1946 Nov 30;84(6):639–660. doi: 10.1084/jem.84.6.639. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. LEVINE S., PUCK T. T., SAGIK B. P. An absolute method for assay of virus hemagglutinins. J Exp Med. 1953 Dec;98(6):521–531. doi: 10.1084/jem.98.6.521. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. LIU O. C., HENLE W. Studies on host-virus interactions in the chick embryo-influenza virus system. IV. The role of inhibitors of hemagglutination in the evaluation of viral multiplication. J Exp Med. 1951 Oct;94(4):269–289. doi: 10.1084/jem.94.4.269. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. LIU O. C., HENLE W. Studies on host-virus interactions in the chick embryo-influenza virus system. V. Simultaneous serial passage of the agents of influenza A and B in relation to variations in the growth cycle of influenza B virus. J Exp Med. 1951 Oct;94(4):291–304. doi: 10.1084/jem.94.4.291. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. LIU O. C., HENLE W. Studies on host-virus interactions in the chick embryo-influenza virus system. VII. Data concerning the significance of infectivity titration end-points and the separation of clones at limiting dilutions. J Exp Med. 1953 Jun;97(6):889–902. doi: 10.1084/jem.97.6.889. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. PAUCKER K., HENLE W. Studies on host-virus interactions in the chick embryo-influenza virus system. XI. The effect of partial inactivation of standard seed virus of 37 degrees C upon the progeny. J Exp Med. 1955 May 1;101(5):479–492. doi: 10.1084/jem.101.5.479. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Rapoport S., Wing M. DIMENSIONAL, OSMOTIC, AND CHEMICAL CHANGES OF ERYTHROCYTES IN STORED BLOOD. I. BLOOD PRESERVED IN SODIUM CITRATE, NEUTRAL, AND ACID CITRATE-GLUCOSE (ACD) MIXTURES. J Clin Invest. 1947 Jul;26(4):591–615. doi: 10.1172/JCI101843. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. SCHLESINGER R. W. Incomplete growth cycle of influenza virus in mouse brain. Proc Soc Exp Biol Med. 1950 Jul;74(3):541–548. doi: 10.3181/00379727-74-17966. [DOI] [PubMed] [Google Scholar]
  22. SCHLESINGER R. W. The relation of functionally deficient forms of influenza virus to viral development. Cold Spring Harb Symp Quant Biol. 1953;18:55–59. doi: 10.1101/sqb.1953.018.01.012. [DOI] [PubMed] [Google Scholar]
  23. TAMM I., TYRRELL D. A. Influenza virus multiplication in the chorioallantoic membrane in vitro: kinetic aspects of inhibition by 5,6-dichloro-1-beta-D-ribofuranosylbenzimidazole. J Exp Med. 1954 Dec 1;100(6):541–562. doi: 10.1084/jem.100.6.541. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. TYRRELL D. A., TAMM I., FORSSMAN O. C., HORSFALL F. L., Jr A new count of allontoic cells of the 10-day chick embryo. Proc Soc Exp Biol Med. 1954 Jul;86(3):594–598. doi: 10.3181/00379727-86-21175. [DOI] [PubMed] [Google Scholar]
  25. Ziegler J. E., Horsfall F. L. INTERFERENCE BETWEEN THE INFLUENZA VIRUSES : I. THE EFFECT OF ACTIVE VIRUS UPON THE MULTIPLICATION OF INFLUENZA VIRUSES IN THE CHICK EMBRYO. J Exp Med. 1944 Apr 1;79(4):361–377. doi: 10.1084/jem.79.4.361. [DOI] [PMC free article] [PubMed] [Google Scholar]

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