首页> 外文期刊>The Journal of Antimicrobial Chemotherapy >In-vitro activity of moxifloxacin against fluoroquinolone-resistant strains of aerobic gram-negative bacilli and Enterococcus faecalis.
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In-vitro activity of moxifloxacin against fluoroquinolone-resistant strains of aerobic gram-negative bacilli and Enterococcus faecalis.

机译:莫西沙星对有氧革兰氏阴性杆菌和粪肠球菌的氟喹诺酮耐药菌株的体外活性。

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摘要

MICs of the new fluoroquinolone, moxifloxacin, and those of ciprofloxacin, ofloxacin and sparfloxacin for 19 genetically characterized fluoroquinolone-resistant strains were determined by the agar dilution method. The MICs of moxifloxacin for Escherichia isolates with one mutation in gyrA (corresponding to Ser83-->Leu or Asp87-->Gly substitution) were 0.25-0.5 mg/L, while those of ciprofloxacin, ofloxacin and sparfloxacin were 0.06-0.25, 1 and 0.12-0.5 mg/L, respectively. These values were four- to 16-fold higher than those of the same antibiotics for the wild-type strain, E. coli KL16. Similar results were observed with clinical isolates of Salmonella spp. harbouring one mutation in gyrA leading to the substitution of Ser83 by Phe or Tyr. In the presence of two mutations in the E. coli gyrA gene, the MICs of moxifloxacin ciprofloxacin, ofloxacin and sparfloxacin were 2, 0.5, 4 and 1 mg/L, respectively; these were 32 times higher than the MICs of these agents for E. coli KL16. The MICs of the four quinolones for triple mutants with two mutations in gyrA and one in parC were even higher, i.e. 8, 8, 16 and 8-16 mg/L, respectively. The MICs of moxifloxacin for Campylobacter coli and Campylobacter jejuni strains with a gyrA mutation leading to Thr86-->Ile substitution ranged from 1 to 2 mg/L, while the MICs of ciprofloxacin, ofloxacin and sparfloxacin were 16-32 mg/L, 8-16 and 4-8 mg/L, respectively. For high-level ciprofloxacin-resistant (MICs of 32 mg/L) clinical isolates of Enterococcus faecalis with one substitution at position 83 in GyrA (E. coli coordinates), the MICs of moxifloxacin, ofloxacin and sparfloxacin were 8-16, > or = 128 and 32 mg/L respectively. In conclusion, moxifloxacin and other fluoroquinolones exhibit cross-resistance against aerobic gram-negative bacilli and enterococci. The in-vitro activity of moxifloxacin was greater than that of ofloxacin and slightly less than that of ciprofloxacin and sparfloxacin against Enterobacteriaceae, but greater than those of the three other compounds tested against Campylobacter spp and E. faecalis.
机译:通过琼脂稀释法确定了新的氟喹诺酮,莫西沙星以及环丙沙星,氧氟沙星和司帕沙星对19种具有遗传特征的耐氟喹诺酮菌株的MIC。莫西沙星对gyrA有一个突变(对应于Ser83-> Leu或Asp87-> Gly取代)的大肠埃希菌分离株的MIC为0.25-0.5 mg / L,而环丙沙星,氧氟沙星和司帕沙星的MICs为0.06-0.25、1和0.12-0.5 mg / L。这些值比野生型大肠杆菌KL16的相同抗生素高4到16倍。用沙门氏菌属的临床分离株观察到相似的结果。在gyrA中带有一个突变,导致Phe或Tyr取代Ser83。在大肠杆菌gyrA基因中存在两个突变的情况下,莫西沙星环丙沙星,氧氟沙星和司帕沙星的MIC分别为2、0.5、4和1 mg / L。这些比这些试剂对大肠杆菌KL16的MIC高32倍。具有gyrA的两个突变和parC的一个突变的三重突变体的四个喹诺酮类药物的MIC甚至更高,分别为8、8、16和8-16 mg / L。导致gyrA突变导致Thr86→Ile取代的gyrA突变的莫西沙星的MIC范围为1-2 mg / L,环丙沙星,氧氟沙星和司帕沙星的MIC值为16-32 mg / L,8分别为-16和4-8 mg / L。对于高环丙沙星耐药性(MICs为32 mg / L)的粪肠球菌临床分离株,在GyrA(大肠杆菌坐标)的第83位有一个取代,莫西沙星,氧氟沙星和司帕沙星的MICs为8-16,>或分别为128和32 mg / L。总之,莫西沙星和其他氟喹诺酮类药物对需氧革兰氏阴性杆菌和肠球菌具有交叉耐药性。莫西沙星的体外活性大于氧氟沙星,但略低于环丙沙星和司帕沙星对肠杆菌的活性,但大于对弯曲杆菌属和屎肠球菌测试的其他三种化合物的体外活性。

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