Jones Ronald N, Kohno Shigeru, Ono Yasuo, Ross James E, Yanagihara Katsunori
JMI Laboratories, North Liberty, IA 52317, USA.
Diagn Microbiol Infect Dis. 2009 Jun;64(2):191-201. doi: 10.1016/j.diagmicrobio.2009.03.001.
The 2007 ZAAPS Program reports the results from the 6th year of oxazolidinone (linezolid) resistance surveillance among Gram-positive pathogens from 23 nations. For 2007, a total of 5591 organisms were systematically sampled from Asia, Australia, Canada, Europe, and Latin America including Staphylococcus aureus (3000 isolates, 38.2% methicillin resistant), coagulase-negative staphylococci (CoNS, 716 isolates), enterococci (906 isolates), Streptococcus pneumoniae (452 isolates), viridans group streptococci (155 isolates), and beta-hemolytic streptococci (362 isolates). The overall linezolid MIC distribution (MIC(50) and MIC(90) at 1 and 2 microg/mL, respectively) was unchanged since 2002. At published linezolid breakpoints (, or = 2 microg/mL), all streptococci were susceptible; however, resistance was observed very rarely among S. aureus (0.03%), CoNS (0.28%), and the enterococci (0.11%, 0.55% intermediate). These oxazolidinone-nonsusceptible isolates occurred in Ireland, Italy, China, and Brazil (9 strains), and the rate was not increased since 2006. The detected mechanism of resistance was G2576 target mutations; no cfr-mediated patterns were observed. Clonal outbreaks with patient-to-patient dissemination were documented in 1 Italian site. Linezolid appears to retain excellent activity against monitored Gram-positive pathogens at a level of >99.8%.
2007年ZAAPS项目报告了来自23个国家的革兰氏阳性病原体对恶唑烷酮类(利奈唑胺)耐药性监测第6年的结果。2007年,共从亚洲、澳大利亚、加拿大、欧洲和拉丁美洲系统采集了5591株微生物,包括金黄色葡萄球菌(3000株分离株,38.2%耐甲氧西林)、凝固酶阴性葡萄球菌(CoNS,716株分离株)、肠球菌(906株分离株)、肺炎链球菌(452株分离株)、草绿色链球菌(155株分离株)和β溶血性链球菌(362株分离株)。自2002年以来,利奈唑胺的总体最低抑菌浓度分布(MIC50和MIC90分别为1和2μg/mL)未发生变化。按照已公布的利奈唑胺断点(≤1μg/mL敏感,≥2μg/mL耐药),所有链球菌均敏感;然而,在金黄色葡萄球菌(0.03%)、CoNS(0.28%)和肠球菌(0.11%,0.55%为中介)中很少观察到耐药情况。这些对恶唑烷酮不敏感的分离株出现在爱尔兰、意大利、中国和巴西(9株),自2006年以来发生率未增加。检测到的耐药机制为G2576靶点突变;未观察到cfr介导的模式。在意大利的1个地点记录到了患者间传播的克隆性暴发。利奈唑胺对监测的革兰氏阳性病原体似乎保持着>99.8%的优异活性。