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加替沙星(BMS 284756)对1999年至2001年亚太地区SENTRY项目临床分离株的抗菌活性。

Antimicrobial activities of garenoxacin (BMS 284756) against Asia-Pacific region clinical isolates from the SENTRY program, 1999 to 2001.

作者信息

Christiansen K J, Bell J M, Turnidge J D, Jones R N

机构信息

Royal Perth Hospital, Australia.

出版信息

Antimicrob Agents Chemother. 2004 Jun;48(6):2049-55. doi: 10.1128/AAC.48.6.2049-2055.2004.

Abstract

Between 1999 and 2001, 16,731 isolates from the Asia-Pacific Region were tested in the SENTRY Program for susceptibility to six fluoroquinolones including garenoxacin. Garenoxacin was four- to eightfold less active against Enterobacteriaceae than ciprofloxacin, although both drugs inhibited similar percentages at 1 microg/ml. Garenoxacin was more active against gram-positive species than all other fluoroquinolones except gemifloxacin. For Staphylococcus aureus, oxacillin resistance was high in many participating countries (Japan, 67%; Taiwan, 60%; Hong Kong, 55%; Singapore, 52%), with corresponding high levels of ciprofloxacin resistance (57 to 99%) in oxacillin-resistant S. aureus (ORSA). Of the ciprofloxacin-resistant ORSA isolates, the garenoxacin MIC was >4 microg/ml for only 9% of them. For Streptococcus pneumoniae, penicillin nonsusceptibility and macrolide resistance were high in many countries. No relationship was seen between penicillin and garenoxacin susceptibility, with all isolates being susceptible at <2 microg/ml. There was, however, a partial correlation between ciprofloxacin and garenoxacin MICs. For ciprofloxacin-resistant isolates for which garenoxacin MICs were 0.25 to 1 microg/liter, mutations in both the ParC and GyrA regions of the quinolone resistance-determining region could be demonstrated. No mutations conferring high-level resistance were detected. Garenoxacin shows useful activity against a wide range of organisms from the Asia-Pacific region. In particular, it has good activity against S. aureus and S. pneumoniae, although there is evidence that low-level resistance is present in those organisms with ciprofloxacin resistance.

摘要

1999年至2001年期间,亚太地区的16731株分离菌在SENTRY项目中接受了对包括加替沙星在内的六种氟喹诺酮类药物的敏感性测试。加替沙星对肠杆菌科细菌的活性比环丙沙星低4至8倍,尽管两种药物在1微克/毫升时抑制的百分比相似。除吉米沙星外,加替沙星对革兰氏阳性菌的活性高于所有其他氟喹诺酮类药物。对于金黄色葡萄球菌,许多参与国家(日本,67%;台湾,60%;香港,55%;新加坡,52%)的苯唑西林耐药率很高,耐苯唑西林金黄色葡萄球菌(ORSA)中环丙沙星耐药率相应较高(57%至99%)。在环丙沙星耐药的ORSA分离株中,加替沙星的最低抑菌浓度(MIC)>4微克/毫升的仅占9%。对于肺炎链球菌,许多国家的青霉素不敏感性和大环内酯类耐药率很高。未发现青霉素与加替沙星敏感性之间的关系,所有分离株在<2微克/毫升时均敏感。然而,环丙沙星和加替沙星的MIC之间存在部分相关性。对于环丙沙星耐药且加替沙星MIC为0.25至1微克/升的分离株,可证明喹诺酮耐药决定区的ParC和GyrA区域均发生了突变。未检测到导致高水平耐药的突变。加替沙星对亚太地区的多种微生物显示出有效的活性。特别是,它对金黄色葡萄球菌和肺炎链球菌具有良好的活性,尽管有证据表明对环丙沙星耐药的这些微生物中存在低水平耐药。

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本文引用的文献

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