JMI Laboratories, 345 Beaver Kreek Center, Suite A, North Liberty, IA 52317, USA.
J Clin Microbiol. 2010 Feb;48(2):568-74. doi: 10.1128/JCM.01384-09. Epub 2009 Nov 25.
A total of 565 methicillin-resistant Staphylococcus aureus (MRSA) isolates were collected mostly from Europe and the Americas (2004 to 2007) during a phase IV clinical trial comparing linezolid with vancomycin for the treatment of complicated skin and skin structure infections proven to be due to MRSA. The isolates were tested for their susceptibilities by the broth microdilution method, they were tested for inducible clindamycin resistance by the D-test, and they were screened for heterogeneous resistance to vancomycin (heterogeneously vancomycin-intermediate S. aureus [hVISA]) by the Etest macromethod. The isolates were evaluated for the MRSA genotype by pulsed-field gel electrophoresis, staphylococcal protein A (spa) typing, multilocus sequence typing (MLST), and staphylococcal cassette chromosome mec (SCCmec) typing. All isolates were inhibited by 4 microg/ml of linezolid (MIC(50) and MIC(90), 2 and 4 microg/ml, respectively). The vast majority of isolates (92.4%) were resistant to erythromycin, and high clindamycin resistance rates were observed (28.5% constitutive and 16.3% inducible). Only 1.0% of the isolates were hVISA. Isolates from the United States were predominantly USA300 sequence type 8 (ST8)-SCCmec type IV (78.5%), followed by a lower prevalence of USA100 ST5-SCCmec type II isolates (14.2%). Strains belonging to the ST5 lineage were widely distributed in Portugal, South American countries, and Mexico. MRSA strains belonging to ST8-SCCmec type IV predominated in Russia (80.0%) and also emerged in Venezuela and Colombia. The epidemic MRSA type 15 clone predominated in the United Kingdom (55.6%) and Spain (100%). In addition, a new MLST profile (ST1071) was observed in South Africa. This study demonstrated the presence of major clones in particular regions (ST8 in the United States, ST5 in Latin America and Portugal, ST22 in Spain and the United Kingdom); however, emerging clones were identified, suggesting that the epidemiology of MRSA continues to evolve.
共收集了 565 株耐甲氧西林金黄色葡萄球菌(MRSA)分离株,主要来自欧洲和美洲(2004 年至 2007 年),这些分离株来自一项比较利奈唑胺与万古霉素治疗确诊为耐甲氧西林金黄色葡萄球菌引起的复杂性皮肤和皮肤结构感染的 IV 期临床试验。采用肉汤微量稀释法检测分离株的药敏性,D 试验检测诱导型克林霉素耐药性,Etest 宏法检测异质性万古霉素中介金黄色葡萄球菌(hVISA)。采用脉冲场凝胶电泳、葡萄球菌蛋白 A(spa)分型、多位点序列分型(MLST)和葡萄球菌盒式染色体 mec(SCCmec)分型对 MRSA 基因型进行评估。所有分离株均被 4μg/ml 的利奈唑胺抑制(MIC(50)和 MIC(90)分别为 2μg/ml 和 4μg/ml)。绝大多数分离株(92.4%)对红霉素耐药,克林霉素耐药率较高(28.5%为固有耐药,16.3%为诱导耐药)。仅 1.0%的分离株为 hVISA。来自美国的分离株主要为 USA300 序列型 8(ST8)-SCCmec 型 IV(78.5%),其次是 USA100 ST5-SCCmec 型 II 分离株的流行率较低(14.2%)。属于 ST5 谱系的菌株广泛分布于葡萄牙、南美国家和墨西哥。属于 ST8-SCCmec 型 IV 的 MRSA 菌株在俄罗斯(80.0%)流行,在委内瑞拉和哥伦比亚也有出现。流行的 MRSA 15 克隆在英国(55.6%)和西班牙(100%)占主导地位。此外,南非还发现了一种新的 MLST 谱型(ST1071)。本研究表明特定地区存在主要克隆(美国的 ST8、拉丁美洲和葡萄牙的 ST5、西班牙和英国的 ST22);然而,也发现了新兴克隆,表明 MRSA 的流行病学仍在不断演变。