"Conjugal" transfer of plasmid DNA among oral streptococci.
Journal: 1978/October - Proceedings of the National Academy of Sciences of the United States of America
ISSN: 0027-8424
PUBMED: 277950
Abstract:
The beta plasmid from Streptococcus faecalis strain DS5, which codes for resistance to erythromycin and lincomycin, was introduced into a Lancefield group F streptococcus, strain DR1501, by transformation. This strain, DR1501 (beta), was found to be an excellent donor of the beta plasmid and readily transferred the resistance markers to various lactic acid bacteria, including certain strains of S. mutans, S. sanguis, and S. salivarius. Evidence is presented indicating that the transfer of the beta plasmid is mediated by a mechanism that requires cell-to-cell contact. The transfer of plasmid DNA during conjugation has been confirmed by the isolation of beta plasmid from transconjugant clones and by their ability to then serve as donors of the erythromycin and lincomycin resistance markers.
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Proc Natl Acad Sci U S A 75(7): 3484-3487

"Conjugal" transfer of plasmid DNA among oral streptococci.

Abstract

The beta plasmid from Streptococcus faecalis strain DS5, which codes for resistance to erythromycin and lincomycin, was introduced into a Lancefield group F streptococcus, strain DR1501, by transformation. This strain, DR1501 (beta), was found to be an excellent donor of the beta plasmid and readily transferred the resistance markers to various lactic acid bacteria, including certain strains of S. mutans, S. sanguis, and S. salivarius. Evidence is presented indicating that the transfer of the beta plasmid is mediated by a mechanism that requires cell-to-cell contact. The transfer of plasmid DNA during conjugation has been confirmed by the isolation of beta plasmid from transconjugant clones and by their ability to then serve as donors of the erythromycin and lincomycin resistance markers.

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  • RAYCROFT RE, ZIMMERMAN LN. NEW MODE OF GENETIC TRANSFER IN STREPTOCOCCUS FAECALIS VAR. LIQUEFACIENS. J Bacteriol. 1964 Apr;87:799–801.[PMC free article] [PubMed] [Google Scholar]
  • Jacob AE, Hobbs SJ. Conjugal transfer of plasmid-borne multiple antibiotic resistance in Streptococcus faecalis var. zymogenes. J Bacteriol. 1974 Feb;117(2):360–372.[PMC free article] [PubMed] [Google Scholar]
  • Jacob AE, Douglas GJ, Hobbs SJ. Self-transferable plasmids determining the hemolysin and bacteriocin of Streptococcus faecalis var. zymogenes. J Bacteriol. 1975 Mar;121(3):863–872.[PMC free article] [PubMed] [Google Scholar]
  • Dunny GM, Clewell DB. Transmissible toxin (hemolysin) plasmid in Streptococcus faecalis and its mobilization of a noninfectious drug resistance plasmid. J Bacteriol. 1975 Nov;124(2):784–790.[PMC free article] [PubMed] [Google Scholar]
  • van Embden JD, Engel HW, van Klingeren B. Drug resistance in group D streptococci of clinical and nonclinical origin: prevalence, transferability, and plasmid properties. Antimicrob Agents Chemother. 1977 Jun;11(6):925–932.[PMC free article] [PubMed] [Google Scholar]
  • Oliver DR, Brown BL, Clewell DB. Characterization of plasmids determining hemolysin and bacteriocin production in Streptococcus faecalis 5952. J Bacteriol. 1977 May;130(2):948–950.[PMC free article] [PubMed] [Google Scholar]
  • Clewell DB, Yagi Y, Dunny GM, Schultz SK. Characterization of three plasmid deoxyribonucleic acid molecules in a strain of Streptococcus faecalis: identification of a plasmid determining erythromycin resistance. J Bacteriol. 1974 Jan;117(1):283–289.[PMC free article] [PubMed] [Google Scholar]
  • Wittenberger CL, Beaman AJ, Lee LN. Tween 80 effect on glucosyltransferase synthesis by Streptococcus salivarius. J Bacteriol. 1978 Jan;133(1):231–239.[PMC free article] [PubMed] [Google Scholar]
  • LeBlanc DJ, Hassell FP. Transformation of Streptococcus sanguis Challis by plasmid deoxyribonucleic acid from Streptococcus faecalis. J Bacteriol. 1976 Oct;128(1):347–355.[PMC free article] [PubMed] [Google Scholar]
  • Currier TC, Nester EW. Isolation of covalently closed circular DNA of high molecular weight from bacteria. Anal Biochem. 1976 Dec;76(2):431–441. [PubMed] [Google Scholar]
  • Meyers JA, Sanchez D, Elwell LP, Falkow S. Simple agarose gel electrophoretic method for the identification and characterization of plasmid deoxyribonucleic acid. J Bacteriol. 1976 Sep;127(3):1529–1537.[PMC free article] [PubMed] [Google Scholar]
  • Aaij C, Borst P. The gel electrophoresis of DNA. Biochim Biophys Acta. 1972 May 10;269(2):192–200. [PubMed] [Google Scholar]
  • Leblanc DJ, Cohen L, Jensen L. Transformation of group F streptococci by plasmid DNA. J Gen Microbiol. 1978 May;106(1):49–54. [PubMed] [Google Scholar]
Abstract
The beta plasmid from Streptococcus faecalis strain DS5, which codes for resistance to erythromycin and lincomycin, was introduced into a Lancefield group F streptococcus, strain DR1501, by transformation. This strain, DR1501 (beta), was found to be an excellent donor of the beta plasmid and readily transferred the resistance markers to various lactic acid bacteria, including certain strains of S. mutans, S. sanguis, and S. salivarius. Evidence is presented indicating that the transfer of the beta plasmid is mediated by a mechanism that requires cell-to-cell contact. The transfer of plasmid DNA during conjugation has been confirmed by the isolation of beta plasmid from transconjugant clones and by their ability to then serve as donors of the erythromycin and lincomycin resistance markers.
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