dWidespread infections with community-associated (CA) methicillin-resistant Staphylococcus aureus (MRSA) have occurred in the United States with the dissemination of the USA300 strain beginning in 2000. We examined 105 isolates obtained from children treated at the University of Chicago from 1994 to 1997 (75 methicillin-susceptible S. aureus [MSSA] and 30 MRSA isolates) in order to investigate for possible evidence of USA300 during this period. Infections were defined epidemiologically based on medical record review. The isolates underwent multilocus sequence typing (MLST), as well as assays for the Panton-Valentine leukocidin (PVL) genes, the protein A gene (spa), and arcA and opp3, proxy markers for the arginine catabolic mobile element (ACME), characteristic of USA300 MRSA. MRSA isolates also underwent staphylococcal cassette chromosome mec (SCCmec) typing and pulsed-field gel electrophoresis (PFGE) subtyping. MSSA isolates belonged to 17 sequence type (ST) groups. The 12 epidemiologically defined CA-MRSA infection isolates were either ST1 (n ؍ 4) or ST8 (n ؍ 8). They belonged to 3 different PFGE types: USA100 (n ؍ 1), USA400 (n ؍ 5), and USA500 (n ؍ 6). Among the CA-MRSA infection isolates, 8 (67%) were PVL ؉ . None of the MRSA or MSSA isolates contained arcA or opp3. Only one MRSA isolate was USA300 by PFGE. This was a health care-associated (HA) MRSA isolate, negative for PVL, that carried SCCmec type II. USA300 with its characteristic features was not identified in the collection from the years 1994 to 1997.
In the mid-1990s, there was a major shift in the clinical and molecular epidemiology of methicillin-resistant Staphylococcus aureus (MRSA) infections in the United States. One of the first reports of a different epidemiology for MRSA infections was from the children's hospital at the University of Chicago Medical Center (UCMC), in which previously healthy children were found to have MRSA infections (1). Notably, the incidence of MRSA infections among children having no previous exposure to the health care system increased significantly from 1988 -1990 to 1993-1995 at the UCMC. Another report documented rapidly fatal infections in four children in North Dakota and Minnesota from 1997 to 1999 (2). A further rapid increase in the incidence of MRSA disease among previously healthy people was documented at the UCMC in 1998UCMC in to 1999UCMC in (3) and 2004UCMC in to 2005, and in other geographic areas in the United States (5-16). These infections were caused by newly emergent strains of MRSA. Because these infections occurred in community settings, the new strains of MRSA causing these infections were called community-associated (CA) MRSA strains, and the infections, as defined by epidemiologic criteria (4, 6), have been called CA-MRSA infections.CA-MRSA strains have been studied extensively. Pulsed-field gel electrophoresis (PFGE) revealed that the initial strains found in the Midwest, Alaska, and New York belonged to a single clonal group classified as USA400 (17). Since 2000, however...