Reynolds Elinor, Ross Jeremy I, Cove Jonathan H
Division of Microbiology, School of Biochemistry and Molecular Biology, University of Leeds, Leeds LS2 9JT, UK.
Int J Antimicrob Agents. 2003 Sep;22(3):228-36. doi: 10.1016/s0924-8579(03)00218-8.
The gene msr(A) confers inducible resistance to 14-membered-ring macrolides and type B streptogramins (MS(B) resistance) in staphylococci. The encoded hydrophilic protein (Msr(A)) is 488 amino acids and contains two ATP-binding motifs characteristic of the ABC transporters. The classical organisation of ABC transporters requires interaction between the two cytoplasmically located ATP-binding domains with two hydrophobic domains positioned in the membrane. Msr(A) appears to mediate drug efflux and yet contains no hydrophobic membrane spanning domains. In addition, Msr(A) functions in previously sensitive heterologous hosts such as Staphylococcus aureus in the absence of other plasmid encoded products. Current research on Msr(A) and related determinants in Gram-positive cocci and in antibiotic producing organisms is reviewed. Alternative hypotheses for the mechanism of action of Msr(A) (i.e. active transport vs. ribosomal protection) are discussed. Evidence indicating Msr(A) may have a role in virulence in addition to conferring antibiotic resistance is also considered.
基因msr(A)赋予葡萄球菌对14元环大环内酯类抗生素和B型链阳菌素(MS(B)耐药性)的诱导抗性。编码的亲水性蛋白(Msr(A))有488个氨基酸,包含两个ABC转运蛋白特有的ATP结合基序。ABC转运蛋白的经典结构需要两个位于细胞质中的ATP结合结构域与两个位于膜中的疏水性结构域之间相互作用。Msr(A)似乎介导药物外排,但不包含疏水性跨膜结构域。此外,在没有其他质粒编码产物的情况下,Msr(A)在先前敏感的异源宿主如金黄色葡萄球菌中发挥作用。本文综述了目前关于革兰氏阳性球菌和抗生素产生菌中Msr(A)及相关决定因素的研究。讨论了Msr(A)作用机制的替代假说(即主动转运与核糖体保护)。还考虑了表明Msr(A)除赋予抗生素抗性外可能在毒力方面起作用的证据。