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. 1960 Mar;24(1):151–166. doi: 10.1128/br.24.1.151-166.1960

VIRAL INTERFERENCE. SOME CONSIDERATIONS OF BASIC MECHANISMS AND THEIR POTENTIAL RELATIONSHIP TO HOST RESISTANCE1

Robert R Wagner a
PMCID: PMC441044  PMID: 16350163

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Selected References

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

  1. ADA G. L., PERRY B. T. Influenza virus nucleic acid: relationship between biological characteristics of the virus particle and properties of the nucleic acid. J Gen Microbiol. 1956 Jul;14(3):623–633. doi: 10.1099/00221287-14-3-623. [DOI] [PubMed] [Google Scholar]
  2. AMES B. N., DUBIN D. T., ROSENTHAL S. M. Presence of polyamines in certain bacterial viruses. Science. 1958 Apr 11;127(3302):814–815. doi: 10.1126/science.127.3302.814-a. [DOI] [PubMed] [Google Scholar]
  3. BALUDA M. A. Homologous interference by ultraviolet-inactivated Newcastle disease virus. Virology. 1957 Aug;4(1):72–96. doi: 10.1016/0042-6822(57)90044-2. [DOI] [PubMed] [Google Scholar]
  4. BALUDA M. A. Loss of viral receptors in homologous interference by ultraviolet-irradiated Newcastle disease virus. Virology. 1959 Mar;7(3):315–327. doi: 10.1016/0042-6822(59)90201-6. [DOI] [PubMed] [Google Scholar]
  5. BANG F. B., GEY G. O., FOARD M., MINNEGAN D. Chronic infections produced in cultured cells strains by the virus of eastern equine encephalomyelitis. Virology. 1957 Dec;4(3):404–417. doi: 10.1016/0042-6822(57)90076-4. [DOI] [PubMed] [Google Scholar]
  6. BERGS V. V., HENLE G., DEINHARDT F., HENLE W. Studies on persistent infections of tissue cultures. II. Nature of the resistance to vesicular stomatitis virus. J Exp Med. 1958 Oct 1;108(4):561–572. doi: 10.1084/jem.108.4.561. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. BERTANI G. Infections bacteriophagiques secondaires des bacteries lysogenes. Ann Inst Pasteur (Paris) 1953 Jan;84(1):273–280. [PubMed] [Google Scholar]
  8. BERTANI G. The role of phage in bacterial genetics. Brookhaven Symp Biol. 1956 Feb;(8):50–57. [PubMed] [Google Scholar]
  9. BURKE D. C., ISAACS A. Some factors affecting the production of interferon. Br J Exp Pathol. 1958 Oct;39(5):452–458. [PMC free article] [PubMed] [Google Scholar]
  10. BURNET F. M., FRASER K. B. Studies on recombination with influenza viruses in the chick embryo. I. Invasion of the chick embryo by influenza viruses. Aust J Exp Biol Med Sci. 1952 Dec;30(6):447–458. doi: 10.1038/icb.1952.44. [DOI] [PubMed] [Google Scholar]
  11. BURNET F. M., LIND P. E. A genetic approach to variation in influenza viruses; recombination of characters between the influenza virus A strain NWS and strains of different serological subtypes. J Gen Microbiol. 1951 Feb;5(1):67–82. doi: 10.1099/00221287-5-1-67. [DOI] [PubMed] [Google Scholar]
  12. 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]
  13. CHAMBERS V. C. The prolonged persistence of western equine encephalomyelitis virus in cultures of strain L cells. Virology. 1957 Feb;3(1):62–75. doi: 10.1016/0042-6822(57)90023-5. [DOI] [PubMed] [Google Scholar]
  14. COHEN S. S., ARBOGAST R. Chemical studies in host-virus interactions; the mutual reactivation of T2r virus inactivated by ultraviolet light and the synthesis of desoxyribose nucleic acid. J Exp Med. 1950 Jun 1;91(6):637–650. doi: 10.1084/jem.91.6.637. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. COLTER J. S. Nucleic acid as the carrier of viral activity. Prog Med Virol. 1958;1:1–35. [PubMed] [Google Scholar]
  16. DEINHARDT F., BERGS V. V., HENLE G., HENLE W. Studies on persistent infections of tissue cultures. III. Some quantitative aspects of host cell-virus interactions. J Exp Med. 1958 Oct 1;108(4):573–589. doi: 10.1084/jem.108.4.573. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. DULBECCO R. Mutual exclusion between related phages. J Bacteriol. 1952 Feb;63(2):209–217. doi: 10.1128/jb.63.2.209-217.1952. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Delbrück M. Interference Between Bacterial Viruses: III. The Mutual Exclusion Effect and the Depressor Effect. J Bacteriol. 1945 Aug;50(2):151–170. [PMC free article] [PubMed] [Google Scholar]
  19. Doermann A. H. Lysis and Lysis Inhibition with Escherichia coli Bacteriophage. J Bacteriol. 1948 Feb;55(2):257–276. doi: 10.1128/jb.55.2.257-276.1948. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Dulbecco R. The Number of Particles of Bacteriophage T2 That Can Participate in Intracellular Growth. Genetics. 1949 Mar;34(2):126–132. doi: 10.1093/genetics/34.2.126. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. FAZEKAS DE ST. GROTH S., GRAHAM D. M. The production of incomplete virus particles among influenza strains: experiments in eggs. Br J Exp Pathol. 1954 Feb;35(1):60–74. [PMC free article] [PubMed] [Google Scholar]
  22. FRENCH R. C., GRAHAM A. F., LESLEY S. M., VAN ROOYEN C. E. The contribution of phosphorus from T2r+ bacteriophage to progeny. J Bacteriol. 1952 Nov;64(5):597–607. doi: 10.1128/jb.64.5.597-607.1952. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. GLEDHILL A. W. The interference of mouse hepatitis virus with ectromelia in mice and a possible explanation of its mechanism. Br J Exp Pathol. 1959 Jun;40(3):291–300. [PMC free article] [PubMed] [Google Scholar]
  24. GOTLIEB T., HIRST G. K. The experimental production of combination forms of virus. VI. Reactivation of influenza viruses after inactivation by ultraviolet light. Virology. 1956 Apr;2(2):235–248. doi: 10.1016/0042-6822(56)90019-8. [DOI] [PubMed] [Google Scholar]
  25. GREEN M., HENLE G., DEINHARDT F. Respiration and glycolysis of human cells grown in tissue culture. Virology. 1958 Apr;5(2):206–219. doi: 10.1016/0042-6822(58)90019-9. [DOI] [PubMed] [Google Scholar]
  26. GROUPE V., HERRMANN E. C., Jr, DOUGHERTY R. M. Protection of mice from neurotoxic action of influenza virus by heat inactivated receptor destroying enzyme. Proc Soc Exp Biol Med. 1954 Dec;87(3):636–637. doi: 10.3181/00379727-87-21468. [DOI] [PubMed] [Google Scholar]
  27. HENLE G., DEINHARDT F., BERGS V. V., HENLE W. Studies on persistent infections of tissue cultures. I. General aspects of the system. J Exp Med. 1958 Oct 1;108(4):537–560. doi: 10.1084/jem.108.4.537. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. 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]
  29. HENLE W., HENLE G., DEINHARDT F., BERGS V. V. Studies on persistent infections of tissue cultures. IV. Evidence for the production of an interferon in MCN cells by myxoviruses. J Exp Med. 1959 Oct 1;110:525–541. doi: 10.1084/jem.110.4.525. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. HENLE W. Interference phenomena between animal viruses; a review. J Immunol. 1950 Mar;64(3):203–236. [PubMed] [Google Scholar]
  31. HERSHEY A. D. An upper limit to the protein content of the germinal substance of bacteriophage T2. Virology. 1955 May;1(1):108–127. doi: 10.1016/0042-6822(55)90009-x. [DOI] [PubMed] [Google Scholar]
  32. HERSHEY A. D., CHASE M. Independent functions of viral protein and nucleic acid in growth of bacteriophage. J Gen Physiol. 1952 May;36(1):39–56. doi: 10.1085/jgp.36.1.39. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. HERSHEY A. D. Some minor components of bacteriophage T2 particles. Virology. 1957 Oct;4(2):237–264. doi: 10.1016/0042-6822(57)90061-2. [DOI] [PubMed] [Google Scholar]
  34. HIRST G. K., GOTLIEB T. The experimental production of combination forms of virus. V. Alterations in the virulence of neurotropic influenza virus as a result of mixed infection. Virology. 1955 Jul;1(2):221–235. doi: 10.1016/0042-6822(55)90018-0. [DOI] [PubMed] [Google Scholar]
  35. 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]
  36. HOOK E. W., WAGNER R. R. Hemorrhagic encephalopathy in chicken embryos infected with influenza virus. I. Factors influencing the development of hemorrhages. Bull Johns Hopkins Hosp. 1958 Sep;103(3):125–139. [PubMed] [Google Scholar]
  37. Ho M., Enders J. F. AN INHIBITOR OF VIRAL ACTIVITY APPEARING IN INFECTED CELL CULTURES. Proc Natl Acad Sci U S A. 1959 Mar;45(3):385–389. doi: 10.1073/pnas.45.3.385. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. ISAACS A., BURKE D. C., FADEEVA L. Effect of interferon on the growth of viruses on the chick chorion. Br J Exp Pathol. 1958 Oct;39(5):447–451. [PMC free article] [PubMed] [Google Scholar]
  39. ISAACS A., BURKE D. C. Mode of action of interferon. Nature. 1958 Oct 18;182(4642):1073–1074. doi: 10.1038/1821073a0. [DOI] [PubMed] [Google Scholar]
  40. ISAACS A., EDNEY M. Interference between inactive and active influenza viruses in the chick embryo. Aust J Exp Biol Med Sci. 1950 Nov;28(6):635–645. doi: 10.1038/icb.1950.66. [DOI] [PubMed] [Google Scholar]
  41. ISAACS A., LINDENMANN J., VALENTINE R. C. Virus interference. II. Some properties of interferon. Proc R Soc Lond B Biol Sci. 1957 Sep 12;147(927):268–273. doi: 10.1098/rspb.1957.0049. [DOI] [PubMed] [Google Scholar]
  42. ISAACS A. Metabolic effects of interferon on chick fibroblasts. Virology. 1960 Jan;10:144–146. doi: 10.1016/0042-6822(60)90012-x. [DOI] [PubMed] [Google Scholar]
  43. 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]
  44. ISAACS A., WESTWOOD M. A. Inhibition by interferon of the growth of vaccinia virus in the rabbit skin. Lancet. 1959 Sep 12;2(7098):324–325. doi: 10.1016/s0140-6736(59)91361-3. [DOI] [PubMed] [Google Scholar]
  45. LE CLERC J. Action of ribonuclease on the multiplication of the influenza virus. Nature. 1956 Mar 24;177(4508):578–579. doi: 10.1038/177578b0. [DOI] [PubMed] [Google Scholar]
  46. LEDERBERG S. Suppression of the multiplication of heterologous bacteriophages in lysogenic bacteria. Virology. 1957 Jun;3(3):496–513. doi: 10.1016/0042-6822(57)90006-5. [DOI] [PubMed] [Google Scholar]
  47. LESLEY S. M., FRENCH R. C., GRAHAM A. F., van ROOYEN C. E. Studies on the relationship between virus and host cell. II. The breakdown of T2r+ bacteriophage upon infection of its host Escherichia coli. Can J Med Sci. 1951 Jun;29(3):128–143. doi: 10.1139/cjms51-017. [DOI] [PubMed] [Google Scholar]
  48. LEVINE L., BARLOW J. L., VAN VUNAKIS H. An internal protein in T2 and T4 bacteriophages. Virology. 1958 Dec;6(3):702–717. doi: 10.1016/0042-6822(58)90116-8. [DOI] [PubMed] [Google Scholar]
  49. LEVINE S. Dynamics of heterologous interference between viable viruses in chick embryo fibroblast mono-layers. Virology. 1958 Feb;5(1):150–167. doi: 10.1016/0042-6822(58)90012-6. [DOI] [PubMed] [Google Scholar]
  50. LINDENMANN J., BURKE D. C., ISAACS A. Studies on the production, mode of action and properties of interferon. Br J Exp Pathol. 1957 Oct;38(5):551–562. [PMC free article] [PubMed] [Google Scholar]
  51. LWOFF A., GUTMANN A. Recherches sur un Bacillus megatherium lysogène. Ann Inst Pasteur (Paris) 1950 Jun;78(6):711–739. [PubMed] [Google Scholar]
  52. LWOFF A. Lysogeny. Bacteriol Rev. 1953 Dec;17(4):269–337. doi: 10.1128/br.17.4.269-337.1953. [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. PAUCKER K., HENLE W. Interference between inactivated and active influenza viruses in the chick embryo. II. Interference by incomplete forms of influenza virus. Virology. 1958 Aug;6(1):198–214. doi: 10.1016/0042-6822(58)90069-2. [DOI] [PubMed] [Google Scholar]
  54. POWELL W. F., POLLARD E. C. The effect of ionizing radiation on the interfering property of influenza virus. Virology. 1956 Jun;2(3):321–336. doi: 10.1016/0042-6822(56)90027-7. [DOI] [PubMed] [Google Scholar]
  55. POWELL W. F., SETLOW R. B. The effect of monochromatic ultraviolet radiation on the interfering property of influenza virus. Virology. 1956 Jun;2(3):337–343. doi: 10.1016/0042-6822(56)90028-9. [DOI] [PubMed] [Google Scholar]
  56. PUCK T. T., LEE H. H. Mechanism of cell wall penetration by viruses. II. Demonstration of cyclic permeability change accompanying virus infection of Escherichia coli B cells. J Exp Med. 1955 Feb 1;101(2):151–175. doi: 10.1084/jem.101.2.151. [DOI] [PMC free article] [PubMed] [Google Scholar]
  57. SABIN A. B. Noncytopathogenic variants of poliomyelitis viruses and resistance to superinfection in tissue culture. Science. 1954 Aug 27;120(3113):357–357. doi: 10.1126/science.120.3113.357. [DOI] [PubMed] [Google Scholar]
  58. 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]
  59. SCHLESINGER R. W. Studies on interference between influenza and equine encephalomyelitis viruses. Arch Gesamte Virusforsch. 1951;4(4):501–517. doi: 10.1007/BF01241169. [DOI] [PubMed] [Google Scholar]
  60. TYRRELL D. A., TAMM I. Prevention of virus interference by 2,5-dimethylbenzimidazole. J Immunol. 1955 Jul;75(1):43–49. [PubMed] [Google Scholar]
  61. VISCONTI N. Resistance to lysis from without in bacteria infected with T2 bacteriophage. J Bacteriol. 1953 Sep;66(3):247–253. doi: 10.1128/jb.66.3.247-253.1953. [DOI] [PMC free article] [PubMed] [Google Scholar]
  62. WAGNER R. R. Acquired resistance in mice to the neurotoxic action of influenza viruses. Br J Exp Pathol. 1952 Apr;33(2):157–167. [PMC free article] [PubMed] [Google Scholar]
  63. WAGNER R. R., SNYDER R. M., HOOK E. W., LUTTRELL C. N. Effect of bacterial endotoxin on resistance of mice to viral encephalitides; including comparative studies of the interference phenomenon. J Immunol. 1959 Jul;83(1):87–98. [PubMed] [Google Scholar]
  64. WATSON J. D. The properties of x-ray inactivated bacteriophage. I. Inactivation by direct effect. J Bacteriol. 1950 Dec;60(6):697–718. doi: 10.1128/jb.60.6.697-718.1950. [DOI] [PMC free article] [PubMed] [Google Scholar]
  65. WEIGLE J. J., DELBRUCK M. Mutual exclusion between an infecting phage and a carried phage. J Bacteriol. 1951 Sep;62(3):301–318. doi: 10.1128/jb.62.3.301-318.1951. [DOI] [PMC free article] [PubMed] [Google Scholar]
  66. von MAGNUS P. Propagation of the PR8 strain of influenza A virus in chick embryos. II. The formation of incomplete virus following inoculation of large doses of seed virus. Acta Pathol Microbiol Scand. 1951;28(3):278–293. doi: 10.1111/j.1699-0463.1951.tb03693.x. [DOI] [PubMed] [Google Scholar]

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