Staphylococcus aureus is a common cause of soft tissue infection, e.g. impe
tigo, cellulitis, or wound infection, and causes osteomyelitis, arthritis,
bacteremia with metastatic infection, and scalded skin and toxic shock synd
romes. Coagulase-negative staphylococci have become increasingly important
causes of nosocomial bacteremia associated with invasive monitoring, intrav
ascular catheters and prosthetic heart valves or joints. Most staphylococci
produce b-lactamase and are resistant to penicillin. An increasing proport
ion of S. aureus have intrinsic resistance to methicillin (MRSA) and presen
t major problems in hospitals for the control of cross infection. The glyco
peptides, teicoplanin and vancomycin, are the antibiotics of first choice f
or treatment of these infections.
After the first report describing a Japanese clinical isolate of vancomycin
-resistant S, aureus (VRSA), several papers have documented the emergence o
f these microorganisms, Since the development and spreading of this phenome
non which is perceived as a fearsome threat to the already difficult therap
y of nosocomial infections due to the prevalence of heterogeneous vancomyci
n resistance, we found the incidence of MRSA exceeds 35% in our hospital. O
ut of 179 methicillin-resistant S, aureus isolated during 1997-1998, two st
rains (1.1%) gave subclones with vancomycin MICs of 8 mg/L. PFGE showed ide
ntical restriction patterns for both isolates, suggesting transfer of a sin
gle clone between two different patients.