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. 1999 Mar;37(3):664–674. doi: 10.1128/jcm.37.3.664-674.1999

TABLE 1.

Characterization of the S. aureus collections used in this study

Collection Collection code(s)a Geographic originb No. of strains Original purpose for strain collection in this study Description of collections Reference(s) or source
1 United States (CDC)a 59 Multicenter collection of MRSA (63%) and MSSA (37%) strains 35
2 Portugal 184 Nationwide disseminated MRSA strains from hospitals 1
3 Worldwide 66 Generation of strain-specific DNA probes Worldwide collection of MRSA strains 20
4 Italy 49 Genetically unrelated MRSA strains (determined by PFGE), isolated from hospitalized patients (five centers), Sicily, Italy 41
5 Australia 18 Genetically unrelated MRSA strains (determined by PFGE), obtained from four different hospitals 41
6 K2 United States 26 Determination of discriminatory power of the genotyping methods (see Table 4) Community-acquired MRSA strains 46
7 SA, SB, SC United States (CDC) 14 Selection of geographically diverse strains from collection 1 35
8 NC The Netherlands 10 Stability experiment for binary typing probes (see Table 3) Strains isolated from persistant nasal carriers 43
9 RIVM The Netherlands 2 Selection of 1 MRSA strain (Va) and 1 MSSA strain (Ia), from collection no. 10
10 RIVM The Netherlands 49 Epidemiological applications of the diverse genotyping systems (see Table 5) MRSA and MSSA strains from 10 outbreaks in 10 Dutch hospitals This study
11 United Kingdom (NCTC) 2 Mapping of the strain-specific DNA probes (see Fig. 1) S. aureus NCTC 8325 and 8325-4 27, 29
a

K2, community-acquired MRSA strains from a New York City hospital; SA, SB, SC, S. aureus strains from the CDC collection; NC, nasal carrier; RIVM, National Institute of Public Health and the Environment (Bilthoven, The Netherlands). 

b

CDC, Centers for Disease Control and Prevention; NCTC, National Collection of Type Cultures (Central Public Health Laboratory, London, United Kingdom).