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Expression of resistance to tetracyclines in strains of methicillin-resistant Staphylococcus aureus
Abstract
A diverse collection of methicillin-resistant Staphylococcus aureus (MRSA) isolates resistant to tetracycline was screened by PCR for the presence of the resistance determinants tetK, tetL, tetM or tetO. Twenty-four of 66 isolates had tetM alone, 21 had tetK alone and 21 had both tetK and tetM (tetKM). All isolates were tetL- and tetO-negative. MICs of tetracycline, doxycycline and minocycline were evaluated for all isolates with or without preincubation in the presence of subinhibitory concentrations of tetracycline or minocycline. All isolates with one or more tetracycline resistance determinants were resistant to tetracycline 8 mg/L without induction of resistance. Some MRSA isolates of each of these three genotypes showed an unexpected lack of resistance to tetracyclines when the disc diffusion or agar dilution method was applied to uninduced cells. Resistance to tetracycline and doxycycline was greater (two- to four-fold) in tetK cells preincubated with tetracycline (tetK MRSA isolates were susceptible to minocycline </=0.25 mg/L under all conditions tested). For isolates with tetM alone, preincubation with tetracycline or minocycline gave up to a four-fold increase in the level of resistance to doxycycline and minocycline. Induction of doxycycline and minocycline resistance was clearly observed for tetKM isolates when cells were preincubated with minocycline. This study suggests that, despite the results of susceptibility testing, all tetracycline-resistant S. aureus isolates should be treated as resistant to doxycycline, and all tetM-positive isolates should be treated as resistant to all tetracyclines. A double disc diffusion method has been developed to identify inducible resistance to minocycline and to distinguish between tetK, tetM and tetKM isolates.
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“The mechanism of resistance to tetracyclines in S. aureus usually involves active removal of the antibiotic from the bacterial cell and ribosomal protection.”
From Molecular Mechanisms of Drug Resistance in Staphylococcus aureus (2022) · cites this paper as [158]
In the citing paper
“The Tet(M) protein determines resistance to tetracyclines including minocycline and is often the cause of resistance to tetracyclines in S. aureus.”
From Molecular Mechanisms of Drug Resistance in Staphylococcus aureus (2022) · cites this paper as [158]
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Cites
Roberts, M. C. (1996) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.1996.tb00251.x · Cited by 689
Cited by
Strommenger, B., Kettlitz, C., Werner, G., & Witte, W. (2003) · Journal of Clinical Microbiology · doi:10.1128/jcm.41.9.4089-4094.2003 · Cited by 578
Mobile genetic elements of Staphylococcus aureus
Malachowa, N., & DeLeo, F. R. (2010) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-010-0389-4 · Cited by 560
Molecular Mechanisms of Drug Resistance in Staphylococcus aureus
Mlynarczyk-Bonikowska, B., Kowalewski, C., Krolak-Ulinska, A., & Marusza, W. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23158088 · Cited by 412
ABC-F Proteins Mediate Antibiotic Resistance through Ribosomal Protection
Sharkey, L. K. R., Edwards, T. A., & O’Neill, A. J. (2016) · mBio · doi:10.1128/mbio.01975-15 · Cited by 284
Metadata
- Authors
- Trzcinski, K., Cooper, B. S., Hryniewicz, W., & Dowson, C. G.
- Venue
- Journal of Antimicrobial Chemotherapy
- Publisher
- Oxford University Press (OUP)
- Published
- 2000-06-01
- Volume
- 45
- Issue
- 6
- Pages
- 763-770
- ISSN
- 0305-7453 (ISSN-L)
- 1460-2091
- OpenAlex
- W2128213617
- Cited by
- 275
- References
- 1
- FWCI
- 4.14
- Type
- journal article
- Language
- en
- Open access
- closed
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- The paper
- Trzcinski, K., Cooper, B. S., Hryniewicz, W., & Dowson, C. G. (2000). Expression of resistance to tetracyclines in strains of methicillin-resistant Staphylococcus aureus. Journal of Antimicrobial Chemotherapy. https://doi.org/10.1093/jac/45.6.763
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.