Shaw K J, Rather P N, Hare R S, Miller G H
Schering-Plough Research Institute, Kenilworth, New Jersey 07033.
Microbiol Rev. 1993 Mar;57(1):138-63. doi: 10.1128/mr.57.1.138-163.1993.
The three classes of enzymes which inactivate aminoglycosides and lead to bacterial resistance are reviewed. DNA hybridization studies have shown that different genes can encode aminoglycoside-modifying enzymes with identical resistance profiles. Comparisons of the amino acid sequences of 49 aminoglycoside-modifying enzymes have revealed new insights into the evolution and relatedness of these proteins. A preliminary assessment of the amino acids which may be important in binding aminoglycosides was obtained from these data and from the results of mutational analysis of several of the genes encoding aminoglycoside-modifying enzymes. Recent studies have demonstrated that aminoglycoside resistance can emerge as a result of alterations in the regulation of normally quiescent cellular genes or as a result of acquiring genes which may have originated from aminoglycoside-producing organisms or from other resistant organisms. Dissemination of these genes is aided by a variety of genetic elements including integrons, transposons, and broad-host-range plasmids. As knowledge of the molecular structure of these enzymes increases, progress can be made in our understanding of how resistance to new aminoglycosides emerges.
本文综述了使氨基糖苷类药物失活并导致细菌耐药的三类酶。DNA杂交研究表明,不同的基因可编码具有相同耐药谱的氨基糖苷类修饰酶。对49种氨基糖苷类修饰酶的氨基酸序列进行比较,为深入了解这些蛋白质的进化和相关性提供了新线索。从这些数据以及对几个编码氨基糖苷类修饰酶的基因进行突变分析的结果中,初步评估了可能对结合氨基糖苷类药物起重要作用的氨基酸。最近的研究表明,氨基糖苷类耐药性可能源于正常静止的细胞基因调控的改变,或者是由于获得了可能源自产生氨基糖苷类药物的生物体或其他耐药生物体的基因。包括整合子、转座子和广宿主范围质粒在内的多种遗传元件促进了这些基因的传播。随着对这些酶分子结构的了解不断增加,我们对新氨基糖苷类药物耐药性产生机制的认识也将取得进展。