Robillard N J, Scarpa A L
Department of Microbiology, Miles Pharmaceuticals, West Haven, Connecticut 06516.
Antimicrob Agents Chemother. 1988 Apr;32(4):535-9. doi: 10.1128/AAC.32.4.535.
Spontaneous ciprofloxacin-resistant mutants of Pseudomonas aeruginosa PAO2 were isolated on ML agar containing 0.5 microgram of ciprofloxacin per ml (2 times the MIC). The mutants were 8- to 64-fold more resistant to ciprofloxacin and showed complete cross resistance to nalidixic acid, ofloxacin, enoxacin, and norfloxacin. Two chromosomal resistance genes, cfxA and cfxB, were mapped between eda-9001 and phe-2 and near pyrB52 distal to proC130, respectively. The cfxB mutation was identical to a nalB mutation and conferred cross resistance to novobiocin, tetracycline, carbenicillin, and chloramphenicol, suggesting that there is an effect on permeability. DNA gyrase A and B subunits were purified from strain PAO2 (wild type), PAO236 nalA2, PAO4704 cfxA2, and PAO4700 cfxA1 cfxB1. Inhibition of gyrase-mediated DNA supercoiling by ciprofloxacin or nalidixic acid was greatly reduced in preparations derived from each of the mutants. Inhibition studies on reconstituted heterologous gyrase subunits showed that decreased inhibition was dependent on the mutant gyrase A subunit. We conclude that ciprofloxacin resistance in P. aeruginosa PAO2 can occur by mutation in the nalB gene or the gene for DNA gyrase A (formerly nalA).
在每毫升含0.5微克环丙沙星(最低抑菌浓度的2倍)的ML琼脂上分离出铜绿假单胞菌PAO2的自发环丙沙星耐药突变体。这些突变体对环丙沙星的耐药性提高了8至64倍,并对萘啶酸、氧氟沙星、依诺沙星和诺氟沙星表现出完全交叉耐药性。两个染色体耐药基因cfxA和cfxB分别定位于eda - 9001和phe - 2之间以及proC130远端的pyrB52附近。cfxB突变与nalB突变相同,并赋予对新生霉素、四环素、羧苄青霉素和氯霉素的交叉耐药性,这表明对通透性有影响。从菌株PAO2(野生型)、PAO236 nalA2、PAO4704 cfxA2和PAO4700 cfxA1 cfxB1中纯化了DNA促旋酶A和B亚基。环丙沙星或萘啶酸对促旋酶介导的DNA超螺旋的抑制作用在来自每个突变体的制剂中大大降低。对重组异源促旋酶亚基的抑制研究表明,抑制作用的降低取决于突变的促旋酶A亚基。我们得出结论,铜绿假单胞菌PAO2中的环丙沙星耐药性可通过nalB基因或DNA促旋酶A基因(以前的nalA)的突变产生。