Coagulase-negative staphylococci (CoNS) (accuracy of 96.8 vs 78.8%, respectively); isolates from the following species had no precise identification: Staphylococcus haemolyticus, S. simulans, and S. capitis. Both systems were similar in the characterization of methicillin resistance. The higher discrepancies for gene mec detection were observed among species other than S. epidermidis (S. hominis, S. saprophyticus, S. sciuri, S. haemolyticus, S. warneri, S. cohnii), and those with borderline MICs.Key words: coagulase-negative staphylococci -methicillin -automated systems Coagulase-negative staphylococci (CoNS) become important nosocomial pathogens, being, in many institutions, among the main etiological agents of nosocomial bacteremias (Cockerill et al. 1997, Hussain et al. 1998, Petinaki et al. 2001. Many clinical laboratories do not identify CoNS in species level when these microrganisms are detected in blood or in cerebrospinal fluid. However, as the significance of CoNS as pathogens has been increased, it has become more important to know the epidemiology and the pathogenic potential of species, individually. This might be particularly important considering blood culture isolates, since it is often difficult to determine the clinical significance of an individual isolate. There are numerous commercial systems and kits available nowadays for the identification of CoNS species (Kloos & Bannerman 1999).Resistance to methicillin among these microrganisms is a matter of concern because of the high and increasing levels detected. In Brazil, a multicenter study showed that methicillin resistance was observed in 87.7% of CoNS isolated from bloodstream infections (Sader et al. 1999). The accurate detection of methicillin resistance among CoNS isolates in the clinical laboratory is important to guide therapy and to promote the correct use of glycopeptides (Hussain et al. 1998, Yamazumi et al. 2001.This work was performed to evaluate the accuracy of two automated systems in the identification of species and determination of methicillin resistance, considering as gold standard the conventional biochemical tests and the characterization of mecA gene by polymerase chain reaction (PCR), respectively.
MATERIALS AND METHODSBacterial samples -Ninety-four consecutive CoNS isolates were included in the study, coming from blood cultures of patients hospitalized in the Complexo Hospitalar Irmandade Santa Casa de Misericórdia in Porto Alegre. The isolates were kept at -20 o C in skim milk (Difco), plus 20% glycerol. The quality control of the tests was done using the Staphylococcus hominis ATCC 27844, S. epidermidis ATCC 12228, S. saprophyticus CCM 883, S. haemolyticus CCM 2737, and S. aureus ATCC 33591.
Identification of bacterial isolates by conventional biochemical tests -The isolates were identified by conventional biochemical tests based on Manual for Clinical Microbiology (Bannerman 2003). The following test were used: catalase test, coagulase test, clumping factor, urease activity, ornitine decarboxilation, PYRase activi...