BACKGROUND: Methicillin resistant strains of Staphylococcus aureus (MRSA) are an important cause of nosocomial infections. AIM: To determine the genotypes of MRSA strains. MATERIAL AND METHODS: Fifty five strains of MRSA, isolated from patients hospitalized in Hospital Base Valdivia, were studied. The phenotype was determined through MicroScan in all strains and by minimum inhibitory concentration (MIC) in 41. The genotype of the strains was analyzed by a duplex polymerase chain reaction (PCR) of the mecA gene, amplifying eight hypervariable DNA regions associated to such gene. RESULTS: According to MIC, 88% of strains had a pattern of resistance against multiple antimicrobial (penicillin, ampicillin, cephradine, gentamycin, ciprofloxacin, lincomycin and erythromycin). Vancomicin resistan strains were not detected. Only 53 strains (96%) had at least one of the eight hypervariable regions and were classified as MRSA. Genotypic patterns types 15 were the most commonly detected in 38% and 34% of strains, respectively. MicroScan erroneously classified five strains in an incorrect phenotype, according to results obtained with duplex PCR. MIC results did not differ from those of duplex PCR. CONCLUSIONS: Duplex- PCR is a useful tool to detect hyper variable regions associated to mecA gene.
BACKGROUND:Methicillin resistant strains of Staphylococcus aureus (MRSA) are an important cause of nosocomial infections. AIM: To determine the genotypes of MRSA strains. MATERIAL AND METHODS: Fifty five strains of MRSA, isolated from patients hospitalized in Hospital Base Valdivia, were studied. The phenotype was determined through MicroScan in all strains and by minimum inhibitory concentration (MIC) in 41. The genotype of the strains was analyzed by a duplex polymerase chain reaction (PCR) of the mecA gene, amplifying eight hypervariable DNA regions associated to such gene. RESULTS: According to MIC, 88% of strains had a pattern of resistance against multiple antimicrobial (penicillin, ampicillin, cephradine, gentamycin, ciprofloxacin, lincomycin and erythromycin). Vancomicin resistan strains were not detected. Only 53 strains (96%) had at least one of the eight hypervariable regions and were classified as MRSA. Genotypic patterns types 15 were the most commonly detected in 38% and 34% of strains, respectively. MicroScan erroneously classified five strains in an incorrect phenotype, according to results obtained with duplex PCR. MIC results did not differ from those of duplex PCR. CONCLUSIONS: Duplex- PCR is a useful tool to detect hyper variable regions associated to mecA gene.
Authors: G Medina; A L Egea; C Otth; L Otth; H Fernández; J L Bocco; M Wilson; C Sola Journal: Eur J Clin Microbiol Infect Dis Date: 2013-06-14 Impact factor: 3.267
Authors: Cristina Moran Toro; Jack Janvier; Kunyan Zhang; Kevin Fonseca; Dan Gregson; Deirdre Church; Kevin Laupland; Harvey Rabin; Sameer Elsayed; John Conly Journal: Can J Infect Dis Med Microbiol Date: 2014-05 Impact factor: 2.471