Hostname: page-component-7dd5485656-npwhs Total loading time: 0 Render date: 2025-10-31T09:17:38.841Z Has data issue: false hasContentIssue false
  • English
  • Français

Segregation of co-transduced streptomycin and tetracycline resistance in Staphylococcus aureus

Published online by Cambridge University Press:  14 April 2009

W. B. Grubb ,
R. J. O'Reilly  and
J. W. May
W. B. Grubb
Affiliation:
Department of Microbiology, University of Western Australia, School of Medicine, Victoria Square, Perth, Western Australia 6000
R. J. O'Reilly
Affiliation:
Department of Microbiology, University of Western Australia, School of Medicine, Victoria Square, Perth, Western Australia 6000
J. W. May
Affiliation:
Department of Microbiology, University of Western Australia, School of Medicine, Victoria Square, Perth, Western Australia 6000
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.

Extrachromosomal streptomycin and tetracycline resistance in Staphylococcus aureus E169 has been transduced to three different recipients. An analysis of the transductants demonstrates that: (1) in most cases the behaviour of the markers in the transductants is similar to that in the donor; (2) the markers are co-transduced at frequencies of 2–44% and the frequency is highest when the selected marker is streptomycin resistance; (3) in the co-transductants the markers segregate independently, suggesting that they are unlinked.

Information

Type
Research Article
Information
Genetics Research , Volume 20 , Issue 1 , August 1972 , pp. 43 - 50
Copyright
Copyright © Cambridge University Press 1972

References

REFERENCES

Arber, W. (1960). Transduction of chromosomal genes and episomes in Escherichia coli. Virology 11, 273–288.CrossRefGoogle ScholarPubMed
Asheshov, E. H. (1969). The genetics of penicillinase production in Staphylococcus aureus strain PS 80. Journal of General Microbiology 59, 289–301.CrossRefGoogle Scholar
Cruickshank, R. (ed.) (1960). Mackie and McCartney's Handrook of Bacteriology, 10th ed.Edinburgh and London: Livingstone.Google Scholar
Grubb, W. B. & O'Reilly, R. J. (1971). Joint transduction of separate extrachromosomal drug resistance determinants in Staphylococcus aureus E169. Biochemical and Biophysical Research Communications 42, 377–383.CrossRefGoogle ScholarPubMed
Jacob, R., Brenner, S. & Cuzin, F. (1963). On the regulation of DNA replication in bacteria. Cold Spring Harror Symposium of Quantitative Biology 28, 329–347.CrossRefGoogle Scholar
Kasuga, T. & Mitsuhashi, S. (1968). Drug resistance of Staphylococci. VIII. Genetic properties of resistance to tetracycline in Staphylococcus aureus E 169. Japanese Journal of Microbiology 12, 269–273.CrossRefGoogle Scholar
May, J. W. & Houghton, R. H. (1965). A simple multipoint inoculator. Laroratory Practice 14, 168.Google Scholar
May, J. W., Houghton, R. H. & Perret, C. J. (1964). The effect of growth at elevated temperatures on some heritable properties of Staphylococcus aureus. Journal of General Microbiology 37, 157–169.CrossRefGoogle ScholarPubMed
Novick, R. P. (1967). Penicillinase plasmids of Staphylococcus aureus. Federation Proceedings of the Federation of American Societies for Experimental Biology 26, 29–38.Google ScholarPubMed
Richmond, M. H. (1967). Associated diploids involving penicillinase plasmids in Staphylococcus aureus. Journal of General Microbiology 46, 85–93.CrossRefGoogle ScholarPubMed
Richmond, M. H. & Johnston, Joan (1969). The reversible transition of certain genes in Staphylococcus aureus between the integrated and the extra-chromosomal state. Genetical Research 13, 267–274.CrossRefGoogle ScholarPubMed