Abstract
Lysogenization of nonlysogenic strains of Staphylococcus aureus was performed with two different bacteriophages, LS1 and LS2, that were unable to plaque on any of the strains of S. aureus tested. Infection of recipient strains was achieved when protoplasts were inoculated with LS1 or LS2 or when bacterial cultures were simultaneously inoculated with a virulent phage together with LS1 or LS2. Lysogenization was demonstrated by changes in phenotypic characters of the host strain and by liberation of bacteriophages from the modified strains as shown by electron microscopic examination. The lysogenic strains differed from the host strains by the following characters: they were coagulase, deoxyribonuclease, and lipase negative; they were untypable by the basic set of phages; they did not ferment mannitol under anaerobic conditions; and they produced only l-(+)-lactic acid by glucose fermentation. Their cell walls contained less glycine and concomitantly more serine than those of the host strains. Furthermore, they were devoid of protein A. Conversely, some antigenic factors as well as the presence of ribitol in the cell wall teichoic acid, indicated a parental relationship between the host strains and the derived lysogenic ones. Phages LS1 and LS2 could be excluded from the lysogenic strains by invading phages, and the revertant nonlysogenic strains recovered all of the characteristics of the initial host strains. It was thus concluded that the phenomenon described was due to lysogenic conversion. The origin of phages LS1 and LS2 is discussed.
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- Asheshov E. H., Winkler K. C. Staphylococcus aureus strains in the "52, 52A, 80, 81 complex". Nature. 1966 Feb 5;209(5023):638–639. doi: 10.1038/209638b0. [DOI] [PubMed] [Google Scholar]
- BASILLE D., PANTALEON J., ROSSET R., GANDON Y., PETIT A. RECHERCHE ET D'ENOMBREMENT DES STAPHYLOCOQUES PR'ESUM'ES PATHOG'ENES DANS LES PRODUITS ALIMENTAIRES. Ann Inst Pasteur Lille. 1964;15:157–164. [PubMed] [Google Scholar]
- Bradley D. E. Ultrastructure of bacteriophage and bacteriocins. Bacteriol Rev. 1967 Dec;31(4):230–314. doi: 10.1128/br.31.4.230-314.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Clecner B., Sonea S. Acquisition de la propriété hémolytique de type delta par conversion lysogénique chez Staphylococcus aureus. Rev Can Biol. 1966 Sep;25(3):145–148. [PubMed] [Google Scholar]
- De Siervo A. J. Alterations in the phospholipid composition of Escherichia coli B during growth at different temperatures. J Bacteriol. 1969 Dec;100(3):1342–1349. doi: 10.1128/jb.100.3.1342-1349.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Devoyod J. J., Millet L., Mocquot G. Un milieu gélosé pour le dénombrement direct de Staphylococcus aureus: milieu au plasma de porc pour S. aureus (PPSA) Can J Microbiol. 1976 Nov;22(11):1603–1611. [PubMed] [Google Scholar]
- Dickinson A. B., Raibaud P., Mocquot G. Agar medium for the selective enumeration of coagulase-positive Staphylococcus from the rat alimentary tract. J Bacteriol. 1968 Feb;95(2):418–425. doi: 10.1128/jb.95.2.418-425.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dobardzic R., Sonea S. Production d'hémolysines et conversion lysogène chez Staphylococcus aureus. Ann Inst Pasteur (Paris) 1971 Jan;120(1):42–49. [PubMed] [Google Scholar]
- Duval-Iflah Y. Lysogenic conversion of the lipase in Staphylococcus pyogenes group 3 strains. Can J Microbiol. 1972 Sep;18(9):1491–1497. doi: 10.1139/m72-228. [DOI] [PubMed] [Google Scholar]
- Duval-Iflah Y. Recombination in staphylococcal bacteriophages. J Gen Virol. 1972 Aug;16(2):237–243. doi: 10.1099/0022-1317-16-2-237. [DOI] [PubMed] [Google Scholar]
- Duval-Iflah Y., Rousseau M., Expert D. Sélection d'une souche de Staphylococcus pyogenes "guérie" de son prophage après conversion lysogénique. C R Acad Sci Hebd Seances Acad Sci D. 1971 Jul 12;273(2):246–249. [PubMed] [Google Scholar]
- Duval-Iflah Y. Variation du type phagique chez une souche de Staphylococcus pyogenes ensemencée dans le tube digestif de rats axéniques (germ-free) C R Acad Sci Hebd Seances Acad Sci D. 1969 Jan 6;268(1):210–212. [PubMed] [Google Scholar]
- Forsgren A., Nordström K., Philipson L., Sjöquist J. Protein A mutants of Staphylococcus aureus. J Bacteriol. 1971 Jul;107(1):245–250. doi: 10.1128/jb.107.1.245-250.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hearst J. E., Vinograd J. A THREE-COMPONENT THEORY OF SEDIMENTATION EQUILIBRIUM IN A DENSITY GRADIENT. Proc Natl Acad Sci U S A. 1961 Jul;47(7):999–1004. doi: 10.1073/pnas.47.7.999. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jollick J. D. Evidence for bacteriophage conversion in Staphylococcus. Microbios. 1972 Sep-Oct;6(22):97–100. [PubMed] [Google Scholar]
- KORMAN R. Z. COAGULASE-NEGATIVE MUTANTS OF STAPHYLOCOCCUS AUREUS: GENETIC STUDIES. J Bacteriol. 1963 Sep;86:363–369. doi: 10.1128/jb.86.3.363-369.1963. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Korman R. Z. Elevated cell wall serine in pleiotropic staphylococcal mutants. J Bacteriol. 1966 Sep;92(3):762–768. doi: 10.1128/jb.92.3.762-768.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lacey R. W. Transfer of tetracycline-resistance between strains of Staphylococcus aureus in mixed cultures. J Gen Microbiol. 1971 Dec;69(2):229–237. doi: 10.1099/00221287-69-2-229. [DOI] [PubMed] [Google Scholar]
- Leduc M., van Heijenoort J., Kaminski M., Szulmajster J. An unusual type of bacterial cell-wall in a mutant of Bacillus subtilis 168. Eur J Biochem. 1973 Aug 17;37(2):389–400. doi: 10.1111/j.1432-1033.1973.tb02998.x. [DOI] [PubMed] [Google Scholar]
- Lind I. Protein A production in different strains of Staphylococcus aureus under varied growth conditions. Acta Pathol Microbiol Scand B Microbiol Immunol. 1974 Dec;82(6):821–828. doi: 10.1111/j.1699-0463.1974.tb02379.x. [DOI] [PubMed] [Google Scholar]
- Omenn G. S., Friedman J. Isolation of mutants of Staphylococcus aureus lacking extracellular nuclease activity. J Bacteriol. 1970 Mar;101(3):921–924. doi: 10.1128/jb.101.3.921-924.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pillet J., Orta B., Corrieras F. Sérotypie des staphylocoques. Intérêt d'une réduction du nombre des souches types utilisées. Ann Inst Pasteur (Paris) 1967 Sep;113(3):363–374. [PubMed] [Google Scholar]
- ROSENDAL K., BUELOW P., JESSEN O. LYOGENIC CONVERSION IN STAPHYLOCOCCUS AUREUS, TO A CHANGE IN THE PRODUCTION OF EXTRACELLULAR "TWEEN"-SPLITTING ENZYME. Nature. 1964 Dec 19;204:1222–1223. doi: 10.1038/2041222b0. [DOI] [PubMed] [Google Scholar]
- ROUNTREE P. M., ASHESHOV E. H. Further observations on changes in the phage-typying pattern of phage type 80/81 staphylococci. J Gen Microbiol. 1961 Sep;26:111–122. doi: 10.1099/00221287-26-1-111. [DOI] [PubMed] [Google Scholar]
- Rosendal K., Bülow P. Temperate phages influencing lipase production by Staphylococcus aureus. J Gen Microbiol. 1965 Dec;41(3):349–356. doi: 10.1099/00221287-41-3-349. [DOI] [PubMed] [Google Scholar]
- SCHILDKRAUT C. L., MARMUR J., DOTY P. Determination of the base composition of deoxyribonucleic acid from its buoyant density in CsCl. J Mol Biol. 1962 Jun;4:430–443. doi: 10.1016/s0022-2836(62)80100-4. [DOI] [PubMed] [Google Scholar]
- Shaw D. R., Mirelman D., Chatterjee A. N., Park J. T. Ribitol teichoic acid synthesis in bacteriophage-resistant mutants of Staphylococcus aureus H. J Biol Chem. 1970 Oct 10;245(19):5101–5106. [PubMed] [Google Scholar]
- TREVELYAN W. E., PROCTER D. P., HARRISON J. S. Detection of sugars on paper chromatograms. Nature. 1950 Sep 9;166(4219):444–445. doi: 10.1038/166444b0. [DOI] [PubMed] [Google Scholar]
- Vedel F., Quetier F. Physico-chemical characterization of mitochondrial DNA from potato tubers. Biochim Biophys Acta. 1974 Apr 10;340(4):374–387. doi: 10.1016/0005-2787(74)90059-8. [DOI] [PubMed] [Google Scholar]
- Wolin M. J., Archibald A. R., Baddiley J. Changes in wall teichoic acid resulting from mutations of Staphylococcus aureus. Nature. 1966 Jan 29;209(5022):484–486. doi: 10.1038/209484a0. [DOI] [PubMed] [Google Scholar]
- Yoshikawa M., Matsuda F., Naka M., Murofushi E., Tsunematsu Y. Pleiotropic alteration of activities of several toxins and enzymes in mutants of Staphylococcus aureus. J Bacteriol. 1974 Jul;119(1):117–122. doi: 10.1128/jb.119.1.117-122.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]



