Yamada Youichi, Shiota Sumiko, Mizushima Tohru, Kuroda Teruo, Tsuchiya Tomofusa
Department of Molecular Microbiology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Tsushima, Japan.
Biol Pharm Bull. 2006 Apr;29(4):801-4. doi: 10.1248/bpb.29.801.
A DNA fragment conferring drug resistance was cloned from the chromosomal DNA of Staphylococcus aureus N315 using a drug hypersensitive Escherichia coli KAM32 as the host. Although E. coli KAM32 cells were sensitive to many antimicrobial agents, transformed cells harboring a recombinant plasmid carrying the DNA region became resistant to several structurally unrelated antimicrobial agents, such as tetraphenylphosphonium chloride, Hoechst 33342 and norfloxacin. These results suggest that the cloned DNA fragment carries a gene(s) encoding a multidrug efflux pump. We partially determined the nucleotide sequence of the cloned DNA and found the mdeA gene within it. The E. coli cells transformed with the mdeA gene showed efflux activity of Hoechst 33342. On the other hand, S. aureus cells transformed with mdeA showed elevated resistance to doxorubicin, daunorubicin, tetraphenylphosphonium chloride, Hoechst 33342, ethidium bromide and rhodamine 6G. Elevated energy-dependent efflux of ethidium was observed with transformed S. aureus. We found that the mdeA gene was expressed under normal growth conditions in S. aureus N315.
使用对药物敏感的大肠杆菌KAM32作为宿主,从金黄色葡萄球菌N315的染色体DNA中克隆出赋予耐药性的DNA片段。虽然大肠杆菌KAM32细胞对许多抗菌剂敏感,但携带含有该DNA区域的重组质粒的转化细胞对几种结构不相关的抗菌剂产生了抗性,如氯化四苯基鏻、Hoechst 33342和诺氟沙星。这些结果表明,克隆的DNA片段携带编码多药外排泵的基因。我们部分测定了克隆DNA的核苷酸序列,并在其中发现了mdeA基因。用mdeA基因转化的大肠杆菌细胞表现出Hoechst 33342的外排活性。另一方面,用mdeA转化的金黄色葡萄球菌细胞对阿霉素、柔红霉素、氯化四苯基鏻、Hoechst 33342、溴化乙锭和罗丹明6G的抗性增强。在转化的金黄色葡萄球菌中观察到溴化乙锭能量依赖性外排增加。我们发现mdeA基因在金黄色葡萄球菌N315的正常生长条件下表达。