TY - JOUR
T1 - Dissemination of methicillin-resistant staphylococcus aureus USA300 sequence type 8 lineage in Latin America
AU - Reyes, Jinnethe
AU - Rincón, Sandra
AU - Diaz, Lorena
AU - Panesso, Diana
AU - Contreras, Germán A.
AU - Zurita, Jeannete
AU - Carrillo, Carlos
AU - Rizzi, Adele
AU - Guzman, Manuel
AU - Adachi, Javier
AU - Chowdhury, Shahreen
AU - Murray, Barbara E.
AU - Arias, Cesar A.
PY - 2009/12
Y1 - 2009/12
N2 - Background. Methicillin-resistant Staphylococus aureus (MRSA) is an important nosocomial and communityassociated (CA) pathogen. Recently, a variant of the MRSA USA300 clone emerged and disseminated in South America, causing important clinical problems. Methods. S. aureus isolates were prospectively collected (2006-2008) from 32 tertiary hospitals in Colombia, Ecuador, Peru, and Venezuela. MRSA isolates were subjected to antimicrobial susceptibility testing and pulsedfield gel electrophoresis and were categorized as health care-associated (HA)-like or CA-like clones on the basis of genotypic characteristics and detection of genes encoding Panton-Valentine leukocidin and staphylococcal cassette chromosome (SCC) mec IV. In addition, multilocus sequence typing of representative isolates of each major CAMRSA pulsotype was performed, and the presence of USA300-associated toxins and the arcA gene was investigated for all isolates categorized as CA-MRSA. Results. A total of 1570 S. aureus were included; 651 were MRSA (41%)-with the highest rate of MRSA isolation in Peru (62%) and the lowest in Venezuela (26%)-and 71%, 27%, and 2% were classified as HA-like, CA-like, and non-CA/HA-like clones, respectively. Only 9 MRSA isolates were confirmed to have reduced susceptibility to glycopeptides (glycopeptide-intermediate S. aureus phenotype). The most common pulsotype (designated ComA) among the CA-like MRSA strains was found in 96% of isolates, with the majority (81%) having a ≤S6-band difference with the USA300-0114 strain. Representative isolates of this clone were sequence type 8; however, unlike the USA300-0114 strain, they harbored a different SCCmec IV subtype and lacked arcA (an indicator of the arginine catabolic mobile element). Conclusion. A variant CA-MRSA USA300 clone has become established in South America and, in some countries, is endemic in hospital settings.
AB - Background. Methicillin-resistant Staphylococus aureus (MRSA) is an important nosocomial and communityassociated (CA) pathogen. Recently, a variant of the MRSA USA300 clone emerged and disseminated in South America, causing important clinical problems. Methods. S. aureus isolates were prospectively collected (2006-2008) from 32 tertiary hospitals in Colombia, Ecuador, Peru, and Venezuela. MRSA isolates were subjected to antimicrobial susceptibility testing and pulsedfield gel electrophoresis and were categorized as health care-associated (HA)-like or CA-like clones on the basis of genotypic characteristics and detection of genes encoding Panton-Valentine leukocidin and staphylococcal cassette chromosome (SCC) mec IV. In addition, multilocus sequence typing of representative isolates of each major CAMRSA pulsotype was performed, and the presence of USA300-associated toxins and the arcA gene was investigated for all isolates categorized as CA-MRSA. Results. A total of 1570 S. aureus were included; 651 were MRSA (41%)-with the highest rate of MRSA isolation in Peru (62%) and the lowest in Venezuela (26%)-and 71%, 27%, and 2% were classified as HA-like, CA-like, and non-CA/HA-like clones, respectively. Only 9 MRSA isolates were confirmed to have reduced susceptibility to glycopeptides (glycopeptide-intermediate S. aureus phenotype). The most common pulsotype (designated ComA) among the CA-like MRSA strains was found in 96% of isolates, with the majority (81%) having a ≤S6-band difference with the USA300-0114 strain. Representative isolates of this clone were sequence type 8; however, unlike the USA300-0114 strain, they harbored a different SCCmec IV subtype and lacked arcA (an indicator of the arginine catabolic mobile element). Conclusion. A variant CA-MRSA USA300 clone has become established in South America and, in some countries, is endemic in hospital settings.
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U2 - 10.1086/648426
DO - 10.1086/648426
M3 - Article
C2 - 19911971
AN - SCOPUS:72049116026
SN - 1058-4838
VL - 49
SP - 1861
EP - 1867
JO - Clinical Infectious Diseases
JF - Clinical Infectious Diseases
IS - 12
ER -