Robicsek Ari, Jacoby George A, Hooper David C
Massachusetts General Hospital, Boston, MA 02114-2696, USA.
Lancet Infect Dis. 2006 Oct;6(10):629-40. doi: 10.1016/S1473-3099(06)70599-0.
Fluoroquinolone resistance is emerging in gram-negative pathogens worldwide. The traditional understanding that quinolone resistance is acquired only through mutation and transmitted only vertically does not entirely account for the relative ease with which resistance develops in exquisitely susceptible organisms, or for the very strong association between resistance to quinolones and to other agents. The recent discovery of plasmid-mediated horizontally transferable genes encoding quinolone resistance might shed light on these phenomena. The Qnr proteins, capable of protecting DNA gyrase from quinolones, have homologues in water-dwelling bacteria, and seem to have been in circulation for some time, having achieved global distribution in a variety of plasmid environments and bacterial genera. AAC(6')-Ib-cr, a variant aminoglycoside acetyltransferase capable of modifying ciprofloxacin and reducing its activity, seems to have emerged more recently, but might be even more prevalent than the Qnr proteins. Both mechanisms provide low-level quinolone resistance that facilitates the emergence of higher-level resistance in the presence of quinolones at therapeutic levels. Much remains to be understood about these genes, but their insidious promotion of substantial resistance, their horizontal spread, and their co-selection with other resistance elements indicate that a more cautious approach to quinolone use and a reconsideration of clinical breakpoints are needed.
全球范围内,革兰氏阴性病原体中氟喹诺酮耐药性正在出现。传统观点认为喹诺酮耐药性仅通过突变获得且仅垂直传播,这并不能完全解释极易感菌中耐药性相对容易产生的现象,也无法解释对喹诺酮类药物和其他药物耐药性之间的紧密关联。最近发现的编码喹诺酮耐药性的质粒介导水平转移基因可能有助于解释这些现象。Qnr蛋白能够保护DNA促旋酶免受喹诺酮类药物影响,在水生细菌中有同源物,似乎已经传播了一段时间,在各种质粒环境和细菌属中已实现全球分布。AAC(6')-Ib-cr是一种能够修饰环丙沙星并降低其活性的变异氨基糖苷乙酰转移酶,似乎是最近才出现的,但可能比Qnr蛋白更为普遍。这两种机制都提供低水平的喹诺酮耐药性,在治疗水平的喹诺酮类药物存在时促进更高水平耐药性的出现。关于这些基因仍有许多有待了解之处,但它们对大量耐药性的潜在促进作用、水平传播以及与其他耐药元件的共同选择表明,需要对喹诺酮类药物的使用采取更谨慎的方法,并重新考虑临床断点。