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Journal of Bacteriology, June 2000, p. 3345-3352, Vol. 182, No. 12
School of Biological Sciences, University of
Sydney, New South Wales 2006, Australia
Received 3 December 1999/Accepted 20 March 2000
Transcription of the tetA(K) tetracycline resistance
determinant encoded by an IS257-flanked cointegrated copy
of a pT181-like plasmid, located within the chromosomal mec
region of a methicillin-resistant Staphylococcus aureus
isolate, has been investigated. The results demonstrated that
transcription of tetA(K) in this strain is directed by both
an IS257-derived hybrid promoter, which is stronger than the native tetA(K) promoter in the autonomous form of
pT181, and a complete outwardly directed promoter identified within one
end of IS257. Despite lower gene dosage, the chromosomal
configuration was shown to afford a higher level of resistance than
that mediated by pT181 in an autonomous multicopy state. Furthermore,
competition studies revealed that a strain carrying the chromosomal
tetA(K) determinant exhibited a higher level of fitness in
the presence of tetracycline but not in its absence. This finding
suggests that tetracycline has been a selective factor in the emergence of strains carrying a cointegrated pT181-like plasmid in their chromosomes. The results highlight the potential of IS257
to influence the expression of neighboring genes, a property likely to
enhance its capacity to mediate advantageous genetic rearrangements.
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
An IS257-Derived Hybrid Promoter Directs Transcription
of a tetA(K) Tetracycline Resistance Gene in the
Staphylococcus aureus Chromosomal mec
Region
*
Corresponding author. Mailing address: School of
Biological Sciences, Macleay Building A12, University of Sydney,
Sydney, New South Wales 2006, Australia. Phone: 61 2 9351-5035. Fax: 61 2 9351-4771. E-mail: nfirth{at}bio.usyd.edu.au.
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