Critchley Ian A, Blosser-Middleton Renée S, Jones Mark E, Thornsberry Clyde, Sahm Daniel F, Karlowsky James A
Focus Technologies, Inc., Herndon, Virginia, USA.
Antimicrob Agents Chemother. 2003 May;47(5):1689-93. doi: 10.1128/AAC.47.5.1689-1693.2003.
The activity of daptomycin was assessed by using 6,973 gram-positive bacteria isolated at 50 United States hospitals in 2000 and 2001. Among the isolates of Streptococcus pneumoniae (n = 1,163) collected, the rate of penicillin resistance was 16.1%; rates of oxacillin resistance among Staphylococcus aureus isolates (n = 1,018) and vancomycin resistance among Enterococcus faecium isolates (n = 368) were 30.0 and 59.5%, respectively. Multidrug-resistant (MDR) phenotypes (isolates resistant to three or more different chemical classes of antimicrobial agents) accounted for 14.2% of S. pneumoniae isolates, 27.1% of S. aureus isolates, and 58.4% of E. faecium isolates. For all gram-positive species tested, MICs at which 90% of the isolates tested were inhibited (MIC(90)s) and MIC ranges for directed-spectrum agents (daptomycin, quinupristin-dalfopristin, and linezolid) were identical or highly similar for isolates susceptible or resistant to other agents or MDR. Daptomycin had a MIC(90) of 0.12 micro g/ml for both penicillin-susceptible and -resistant isolates of S. pneumoniae. Against oxacillin-resistant S. aureus daptomycin had a MIC(90) of 0.5 micro g/ml, and it had a MIC(90) of 4 micro g/ml against both vancomycin-susceptible and -resistant E. faecium. The MIC(90)s for daptomycin and other directed-spectrum agents were unaffected by the regional or anatomical origin of isolates or patient demographic parameters (patient age, gender, and inpatient or outpatient care). Our results confirm the gram-positive spectrum of activity of daptomycin and that its activity is independent of susceptibility or resistance to commonly prescribed and tested antimicrobial agents. This study may serve as a baseline to monitor future changes in the susceptibility of gram-positive species to daptomycin following its introduction into clinical use.
采用2000年和2001年在美国50家医院分离出的6973株革兰氏阳性菌评估达托霉素的活性。在所收集的肺炎链球菌分离株(n = 1163)中,青霉素耐药率为16.1%;金黄色葡萄球菌分离株(n = 1018)中的苯唑西林耐药率和粪肠球菌分离株(n = 368)中的万古霉素耐药率分别为30.0%和59.5%。多重耐药(MDR)表型(对三种或更多不同化学类别的抗菌药物耐药的分离株)在肺炎链球菌分离株中占14.2%,在金黄色葡萄球菌分离株中占27.1%,在粪肠球菌分离株中占58.4%。对于所有测试的革兰氏阳性菌,对90%测试分离株有抑制作用的最低抑菌浓度(MIC90)以及针对窄谱抗菌药物(达托霉素、奎奴普丁 - 达福普汀和利奈唑胺)的MIC范围,对于对其他药物敏感或耐药或多重耐药的分离株而言是相同的或高度相似的。达托霉素对青霉素敏感和耐药肺炎链球菌分离株的MIC90均为0.12μg/ml。对于苯唑西林耐药的金黄色葡萄球菌,达托霉素的MIC90为0.5μg/ml,对于万古霉素敏感和耐药的粪肠球菌,其MIC90均为4μg/ml。达托霉素和其他窄谱抗菌药物的MIC90不受分离株的地区或解剖学来源或患者人口统计学参数(患者年龄、性别以及住院或门诊治疗)的影响。我们的结果证实了达托霉素的革兰氏阳性菌活性谱,并且其活性与对常用处方和测试抗菌药物的敏感性或耐药性无关。本研究可作为一个基线,用于监测革兰氏阳性菌在达托霉素引入临床使用后对其敏感性的未来变化。