Hostname: page-component-586b7cd67f-dsjbd Total loading time: 0 Render date: 2024-11-23T07:26:22.054Z Has data issue: false hasContentIssue false

Genomic structure of phage F22, a hybrid between serologically and morphologically unrelated Salmonella typhimurium bacteriophages P22 and Fels 2

Published online by Cambridge University Press:  14 April 2009

Nobuto Yamamoto
Affiliation:
Department of Microbiology and Immunology, Hahnemann University School of Medicine, Philadelphia, PA 19102, U.S.A.
Robert J. McDonald
Affiliation:
Department of Microbiology and Immunology, Hahnemann University School of Medicine, Philadelphia, PA 19102, U.S.A.
Rights & Permissions [Opens in a new window]

Summary

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

Salmonella typhimurium phage P22 can recombine with a serologically and morphologically unrelated Salmonella phage Fels 2 to yield the hybrid phage F22 at a frequency of about 10−12. F22 has inherited the entire late genes (protein coat and tail structural genes) of Fels 2 but carries some P22 early genes. P22 genes in the F22 phage were indentified by marker rescue of various P22 mutants. The F22 genome carries the x-erf-c-18-12 segment of the P22 genome. A number of P22 amber mutants were also tested to support these data. The F22 region homologous to P22 was mapped by scoring the ratio of P22 backcross recombinant types in lysates of F22 lysogens superinfected with P22c2ts12. The ratio of the distances between these markers and the ends of the homologous region was determined. Furthermore a new F22 hybrid designated F22dis, containing both P22 immunity regions (c and Im), was isolated at a frequency of about 10−4 by superinfecting F22 lysogens with P22. F22dis phage has lost some Fels 2 gene(s) which have been replaced by the P22 segment containing the Im region, resulting in formation of a defective hybrid phage.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1986

References

Fukuda, S. & Yamamoto, N. (1972). Formation of various genome lengths of hybrids between serologically and morphologically unrelated bacteriophage species. Virology 50, 727732.CrossRefGoogle ScholarPubMed
Gemski, P., Baron, L. S. & Yamamoto, N. (1972). Formation of hybrids between coliphage λ and Salmonella phage P22 with a Salmonella typhimurium hybrid sensitive to these phages. Proceedings of the National Academy of Sciences, USA 69, 31103114.CrossRefGoogle ScholarPubMed
Levine, M. (1971). Mutations in the temperate phage P22 and lysogeny in Salmonella. Virology 3, 2241.CrossRefGoogle Scholar
Levine, M. & Curtiss, R. (1961). Genetic fine structure of the c region and the linkage map of phage P22. Genetics 46, 15731580.CrossRefGoogle Scholar
Levine, M. & Schott, C. (1971). Mutations of phage P22 affecting phage DNA synthesis and lysogenization. Journal of Molecular Biology 62, 5364.CrossRefGoogle ScholarPubMed
Levine, M., Turesdell, S., Ramakrishnan, T. & Bronson, M. J. (1975). Dual control of lysogeny by bacteriophage P22: an antirepressor locus and its controlling elements. Journal of Molecular Biology 91, 421438.CrossRefGoogle ScholarPubMed
Luria, S. E. (1953). General Virology, p. 273. New York: Wiley.Google Scholar
Susskind, M. M. & Botstein, D. (1978). Molecular genetics of bacteriophage P22. Microbiological Reviews 42, 385413.CrossRefGoogle ScholarPubMed
Yamagami, H. & Yamamoto, N. (1970). Contribution of the bacterial recombination function to replication of bacteriophage P22. Journal of Molecular Biology 53, 281285.CrossRefGoogle Scholar
Yamamoto, N. (1969 a). Genetic evolution of bacteriophage. I. Hybrids between unrelated bacteriophages P22 and Fels 2. Proceedings of the National Academy of Sciences, USA 62, 6369.CrossRefGoogle ScholarPubMed
Yamamoto, N. (1969 b). Damage, repair and recombination between the superinfecting phage and the prophage. Virology 38, 447456.CrossRefGoogle ScholarPubMed
Yamamoto, N. (1978). A generalized transducing Salmonella phage ES18 can recombine with a serologically unrelated phage Fels 1. Journal of General Virology 38, 263272.CrossRefGoogle ScholarPubMed
Yamamoto, N. & Anderson, T. F. (1961). Genomic masking and recombination between serologically unrelated phages P22 and P221. Virology 14, 430439.CrossRefGoogle ScholarPubMed
Yamamoto, N., Gemski, P. & Baron, L. S. (1981). Isolation of a hybrid between Salmonella phage P22 and coli mutator phage Mu-1. Abstracts of the Annual Meeting – American Society of Microbiology, p. 115.Google Scholar
Yamamoto, N., Gemski, P. & Baron, L. S. (1983). Genetic studies of hybrids between coliphage φ80 and Salmonella phage P22. Journal of General Virology 64, 199205.CrossRefGoogle Scholar
Yamamoto, N., Ushijima, N., Gemski, P. & Baron, L. S. (1977). Generic studies of hybrids between coliphage λ and Salmonella phage P22: genetic analysis of the P22-λ hybrid class. Molecular and General Genetics 155, 117121.CrossRefGoogle ScholarPubMed
Yamamoto, N. & Weir, M. L. (1966). Boundary structure between homologous and nonhomologous regions in serologically unrelated bacteriophages P22 and P221.I. Mapping by recombinants found in the cultures of double lysogenic strains for P22h and P221. Virology 28, 324329.CrossRefGoogle ScholarPubMed
Yamamoto, N., Wohlhieter, J. A., Gemski, P. & Baron, L. S. (1978). λimm P22dis: a hybrid of coliphage λ with both immunity regions of Salmonella phage P22. Molecular and General Genetics 166, 223243.CrossRefGoogle ScholarPubMed