Enhanced resistance to erythromycin is conferred by the enterococcal msrC determinant in Staphylococcus aureus

被引:20
作者
Reynolds, E [1 ]
Cove, JH [1 ]
机构
[1] Univ Leeds, Sch Biochem & Microbiol, Leeds LS2 9JT, W Yorkshire, England
关键词
macrolide resistance; ABC transporter; molecular cloning; staphylococci; enterococci;
D O I
10.1093/jac/dkh541
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: The msrC gene, found on the chromosome of Enterococcus faecium, shares a high degree of similarity with the staphylococcal erythromycin resistance determinant msr(A). The enterococcal determinant was cloned into Staphylococcus aureus to determine whether msrC could confer antibiotic resistance in staphylococci. Methods: A shuttle vector comprising pBluescript and pSK265 was used to introduce multiple copies of msrC into S. aureus RN4220. The integration vector pCL84 was employed to insert a single copy of msrC into the S. aureus chromosome. MICs were determined by the broth microdilution method. Results: Expression of msrC from both chromosomal and plasmid loci in erythromycin-susceptible S. aureus RN4220 (MIC 0.25 mg/L) gave rise to enhanced protection against erythromycin, with an MIC of 32-64 mg/L for S. aureus RN4220 containing msrC in multiple copies and an MIC of 16-64 mg/L with msrC inserted as a single copy in the S. aureus chromosome. Conclusions: MsrC mediates high-level resistance to erythromycin in S. aureus.
引用
收藏
页码:260 / 264
页数:5
相关论文
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