Abstract
The group A streptococcal bacteriophage SP24 contains a unique phage att site and integrates into a common chromosomal locus in two unrelated group A streptococcal strains, CS24 and CS112. Southern blot analysis suggested that the terminally redundant phage DNA recombines to form the unit-length genome observed in the prophage state. Phage DNA integration appears to be required for stable lysogen formation and conversion to the M+ state; however, the precise role of the bacteriophage and the relationship of phage integration to increased M protein synthesis are unclear.
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- Barksdale L., Arden S. B. Persisting bacteriophage infections, lysogeny, and phage conversions. Annu Rev Microbiol. 1974;28(0):265–299. doi: 10.1146/annurev.mi.28.100174.001405. [DOI] [PubMed] [Google Scholar]
- Fischetti V. A., Gotschlich E. C., Siviglia G., Zabriskie J. B. Streptococcal M protein extracted by nonionic detergent. I. Properties of the antiphagocytic and type-specific molecules. J Exp Med. 1976 Jul 1;144(1):32–53. doi: 10.1084/jem.144.1.32. [DOI] [PMC free article] [PubMed] [Google Scholar]
- LANCEFIELD R. C. Current knowledge of type-specific M antigens of group A streptococci. J Immunol. 1962 Sep;89:307–313. [PubMed] [Google Scholar]
- ROBBINS P. W., UCHIDA T. Determinants of specificity in Salmonella: changes in antigenic structure mediated by bacteriophage. Fed Proc. 1962 Jul-Aug;21:702–710. [PubMed] [Google Scholar]
- Spanier J. G., Cleary P. P. A DNA substitution in the group A streptococcal bacteriophage SP24. Virology. 1983 Oct 30;130(2):514–522. doi: 10.1016/0042-6822(83)90104-6. [DOI] [PubMed] [Google Scholar]
- Spanier J. G., Cleary P. P. A restriction map and analysis of the terminal redundancy in the group a streptococcal bacteriophage SP24. Virology. 1983 Oct 30;130(2):502–513. doi: 10.1016/0042-6822(83)90103-4. [DOI] [PubMed] [Google Scholar]
- Spanier J. G., Cleary P. P. Bacteriophage control of antiphagocytic determinants in group A streptococci. J Exp Med. 1980 Nov 1;152(5):1393–1406. doi: 10.1084/jem.152.5.1393. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Spanier J. G., Jones S. J., Cleary P. Small DNA deletions creating avirulence in Streptococcus pyogenes. Science. 1984 Aug 31;225(4665):935–938. doi: 10.1126/science.6089334. [DOI] [PubMed] [Google Scholar]
- Swanson J., Hsu K. C., Gotschlich E. C. Electron microscopic studies on streptococci. I. M antigen. J Exp Med. 1969 Nov 1;130(5):1063–1091. doi: 10.1084/jem.130.5.1063. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Todd E. W., Lancefield R. C. VARIANTS OF HEMOLYTIC STREPTOCOCCI; THEIR RELATION TO TYPE-SPECIFIC SUBSTANCE, VIRULENCE, AND TOXIN. J Exp Med. 1928 Nov 30;48(6):751–767. doi: 10.1084/jem.48.6.751. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Watson J. D. Origin of concatemeric T7 DNA. Nat New Biol. 1972 Oct 18;239(94):197–201. doi: 10.1038/newbio239197a0. [DOI] [PubMed] [Google Scholar]




