Publications


Epidemic Methicillin-Resistant Staphylococcus aureus (MRSA): from Buenos Aires, Argentina to Ontario, Canada

B. M. WILLEY, G. RUZO, B. SHOPSIN, B. N. KREISWIRTH, A. FAMIGLIETTI, C. VAY, A. McGEER, D. E. LOW.

Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada; Nuestra Senora De Lujan and Hospital de Clinicas, Buenos Aires, Argentina; and PHRI, New York, New York, US.

Background: MRSA rates in the province of Ontario (ON) increased from <500 cases/year prior to 1995 to 8610 in 1998. In 1996, Argentina reported 65% of hospital/clinical S. aureus to be MRSA. This study determined the genetic relationship between MRSA identified in the two countries.

Methods: 56 MRSA from Buenos Aires (BA) (14/1995, 2/1996, 21/1997, 19/1998) were compared to 1083 ON strains (289/1996, 557/1997, 237/1998) using SmaI pulsed field typing (PFGE). All BA and 92 ON MRSA were sub-typed by computerized alignment of proteinA gene repeat sequences (SPA).

Results: PFGE identified 4 major clones: 160 isolates of clone A (143 ON, 17 BA), 142 clone B (109 ON, 33 BA), 784 clone C (all ON), 35 clone D (32 ON, 3 BA), and 18 of other/uncertain clonality (15 ON, 3 BA). The 92 ON MRSA SPA typed included 12/clone A, 25/B, 69/C, 12/D, and 7 of uncertain type. SPA confirmed the PFGE clonal delineation and further divided these clones. PFGE clone A was divisible into 8 SPA types (4 ON, 5 BA); B into 10 types (7 ON, 5 BA); C into 4 types (4 ON only), D into 7 types (4 ON, 3 BA). SPA types 2 (PFGE clone A), 3 and 33 (both clone B) were found among ON and BA MRSA. These SPA types predominated among clones A and B in both countries, and were observed at a constant rate between 1995 and 1998. SPA typing confirmed clone C to be newly emergent in ON and associated with the provinces dramatic increase in MRSA cases. This clone was not found among BA MRSA.

Conclusions: Characterization of MRSA from ON and BA using two validated molecular methods has elucidated the global nature of their dissemination and demonstrated the existence of only a limited number of distinct epidemic clones.

Presented at:

Abstract submitted to the 9th International Congress on Infectious Diseases, Buenos Aires, Argentina, April 10-13, 2000




©Copyright 1999 Last Modified