Vancomycin-heteroresistant phenotype in invasive methicillin-resistant Staphylococcus aureus isolates belonging to spa type 041

被引:26
作者
Monaco, M. [1 ]
Sanchini, A. [1 ]
Grundmann, H. [2 ,3 ]
Pantosti, A. [1 ]
机构
[1] Ist Super Sanita, Dept Infect Parasit & Immune Mediated Dis, I-00161 Rome, Italy
[2] Natl Inst Publ Hlth & Environm, NL-93721 MA Bilthoven, Netherlands
[3] Univ Groningen, Univ Med Ctr Groningen, Dept Med Microbiol, NL-9713 GZ Groningen, Netherlands
关键词
CASSETTE CHROMOSOME MEC; REDUCED SUSCEPTIBILITY; ANTIBIOTIC-RESISTANCE; INFECTIONS; STRAINS; GLYCOPEPTIDES; CLONES; IDENTIFICATION; MULTICENTER; HOSPITALS;
D O I
10.1007/s10096-010-0922-2
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The aim of this study was to characterise invasive methicillin-susceptible Staphylococcus aureus (MSSA) and methicillin-resistant S. aureus (MRSA) strains from Italy and to investigate the presence of heteroresistant vancomycin-intermediate S. aureus (h-VISA). Eighty-two MSSA and 66 MRSA strains obtained from 19 laboratories were submitted to in vitro susceptibility testing; MRSA strains were also analysed by the macro Etest (MET) and vancomycin population analysis profiles (PAP) to detect the presence of h-VISA. Genotyping included the detection of agr locus, SCCmec typing, spa typing and multilocus sequence typing (MLST). By Etest, 66% of all isolates showed a minimum inhibitory concentration (MIC) a parts per thousand yen1.5 mu g/ml and two MRSA strains were categorised as VISA (MIC = 3 mu g/ml). Twelve MRSA strains were positive by MET; of these, 9 (14% of all MRSA) were confirmed as h-VISA by PAP. MRSA strains were assigned to 14 spa types, with t001, t008 and t041 including 77% of the isolates. The most common spa type, t041, characterised as ST228/273-MRSA-I (CC5) and comprising 24 isolates, included one VISA and eight h-VISA. This is the first description of a close association between h-VISA and t041, a spa type common in Italy and in other European countries, that highlights the importance of molecular typing to identify clones of special clinical relevance.
引用
收藏
页码:771 / 777
页数:7
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