Cloning and sequences of inducible and constitutive macrolide resistance genes in Staphylococcus aureus that correspond to an ABC transporter

被引:24
作者
Matsuoka, M
Jánosi, L
Endou, K
Nakajima, Y
机构
[1] Hokkaido Coll Pharm, Div Microbiol, Otaru, Hokkaido 0470264, Japan
[2] Natl Ctr Epidemiol, H-1097 Budapest, Hungary
关键词
msr gene; macrolide resistance; erythromycin resistance; Staphylococcus aureus; active efflux; ABC transporter;
D O I
10.1016/S0378-1097(99)00518-2
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A restriction map was made and the DNA sequence was determined for a plasmid, pMC38, derived from the inducible macrolide resistance plasmid pEP2104, that showed constitutive resistance to PMS: antibiotics (partial macrolide and streptogramin B antibiotics). A 5.04 kb SalI-PstI fragment (fragment C) of pMC38, which encoded PMS resistance, was cloned into a shuttle vector, pRIT5, to yield pMR504. The transformant Staphylococcus aureus 4220 (pMR504) exhibited constitutive PMS resistance. Fragment C was subcloned to pUC19 in order to determine the DNA sequence. This sequence was consequently found to contain three open reading frames (ORF1-3), of which ORF3 corresponded to the 63 kDa membrane protein (MsrSA) that expressed PMS resistance. According to DNA sequence comparison of the control region of ORF3 in pMC38 and pEP2104, 44 nucleolides including RBSI and the leader peptide (MTASMRLK) were deleted on plasmid pMC38, This suggests that the leader peptide is essential for the inducible expression of PMS resistance. (C) 1999 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:91 / 100
页数:10
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