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. 1964 Jun;87(6):1330–1338. doi: 10.1128/jb.87.6.1330-1338.1964

ISOLOGOUS INTERFERENCE WITH ULTRAVIOLET AND X-RAY IRRADIATED BACTERIOPHAGE T21

Stuart B Levy a,2
PMCID: PMC277207  PMID: 14188710

Abstract

Levy, Stuart B. (Institut du Radium, Paris, France). Isologous interference with ultraviolet and X-ray irradiated bacteriophage T2. J. Bacteriol. 87:1330–1338. 1964.—Qualitative and quantitative analysis of the interference capacity of an irradiated T2 bacteriophage was made with ultraviolet and X-ray irradiation. Two different effects were found to explain the total interference picture in the ultraviolet-irradiated system: exclusion and depression. Exclusion is the absolute inhibition of infectious phage growth in the bacterial host. Depression is the diminution of burst size in instances where the infectious phage has not been excluded. Both effects were seen when the infectious phage was added after the addition of ultraviolet-irradiated phage. Doses between 1,600 and 2,200 ergs/mm2 (survivals, ca. 10−7) showed the greatest exclusion effect (70%). Exclusion was lost between 6,500 and 7,500 ergs/mm2. The depression effect was highest (90%) at lower doses (survivals, ca. 10−6), falling off as the dose range went above 1,600 ergs/mm2 or survivals of 10−7. Depression was lost at 3,000 ergs/mm2. X-ray irradiation (both direct and indirect) to survivals less than 10−2 showed no interference capacity in the phage irradiated. Indirect X-ray irradiation to survivals between 5 and 10% showed 50% exclusion, but no depression.

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Selected References

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

  1. 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]
  2. 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]
  3. 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]
  4. 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]
  5. FRENCH R. C., LESLEY S. M., GRAHAM A. F., van ROOYEN C. E. Studies on the relationship between virus and host cell. III. The breakdown of P32 labelled T2r+ bacteriophage adsorbed to E. coli previously infected by other coliphages of the T group. Can J Med Sci. 1951 Jun;29(3):144–148. [PubMed] [Google Scholar]
  6. 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]
  7. ISAACS A., LINDENMANN J. Virus interference. I. The interferon. Proc R Soc Lond B Biol Sci. 1957 Sep 12;147(927):258–267. doi: 10.1098/rspb.1957.0048. [DOI] [PubMed] [Google Scholar]
  8. 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]
  9. Luria S. E., Dulbecco R. Genetic Recombinations Leading to Production of Active Bacteriophage from Ultraviolet Inactivated Bacteriophage Particles. Genetics. 1949 Mar;34(2):93–125. doi: 10.1093/genetics/34.2.93. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Luria S. E., Exner F. M. The Inactivation of Bacteriophages by X-Rays-Influence of the Medium. Proc Natl Acad Sci U S A. 1941 Aug 15;27(8):370–375. doi: 10.1073/pnas.27.8.370. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. WAGNER R. R. Cellular resistance to viral infection, with particular reference to endogenous interferon. Bacteriol Rev. 1963 Mar;27:72–86. doi: 10.1128/br.27.1.72-86.1963. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. 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]
  13. WATSON J. D. The properties of x-ray inactivated bacteriophage. J Bacteriol. 1952 Apr;63(4):473–485. doi: 10.1128/jb.63.4.473-485.1952. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Wagner R. R. VIRAL INTERFERENCE. SOME CONSIDERATIONS OF BASIC MECHANISMS AND THEIR POTENTIAL RELATIONSHIP TO HOST RESISTANCE. Bacteriol Rev. 1960 Mar;24(1):151–166. doi: 10.1128/br.24.1.151-166.1960. [DOI] [PMC free article] [PubMed] [Google Scholar]

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