Treatment of severe enterococcal infection requires combined therapy to achieve a synergistic bactericidal effect [35]. However, the results obtained in cases of severe infections associated with enterococci have shown that HLAR should not be treated with combined therapy (gentamicin/ampicillin) [35]. Therefore, the treatment of HLAR E. faecium is restricted [36]. The enterococcal surface protein Esp, which is encoded by genes that appear to have been acquired and localized within a pathogenicity island, is commonly found in clinical Dibutyryl-cAMP ic50 isolates and

anchors to the cell wall. This protein LY2874455 molecular weight also affects biofilm formation and plays a role in experimental UTI and/or endocarditis models [2]. The presence of the esp gene has been associated with hospital outbreaks, although this gene is not exclusively found in epidemic strains [19, 30, 37, 38]. The esp gene was detected in 83.3% of our VREF clinical isolates. In addition, the majority of esp + strains of E. faecium isolates were multidrug-resistant

NVP-BGJ398 to more than three antibiotics, in accord with data reported by other researchers [39–41]. On the other hand, the hyl gene was found in 50% of the VREF clinical isolates and displayed a higher prevalence compared to the prevalences of 29.8% (29/131) reported in isolates of E. faecium in the Picardy Region of France, 38% (83/220) in isolates from the US and 3% in European clinical isolates. However, in the United Kingdom, a hyl gene prevalence of 71% (20/28) was observed in E. faecium isolates [14, 42, 43]. We believe that the differences observed in the detection

rates of the hyl gene are due to the region in which the samples were isolated. The rates of the occurrence of esp +/hyl -, esp +/hyl + and esp -/hyl + isolates were found to be 50% (6/12), 33.3% (4/12) and 16.7% (2/12), respectively, which is in accord with the findings of Vankerckhoven et al. and Rice et al. [14, 42, 44]. The VREF clinical isolates of Mexican origin in which the esp Epothilone B (EPO906, Patupilone) and/or hyl gene was amplified (alone or together), were resistant to more than three antibiotics; in contrast, other studies have shown a significant correlation between the presence of the esp gene and resistance to ampicillin, imipenem and ciprofloxacin [40, 41]. PFGE and MLST analyses have been proposed as alternative methods for the molecular characterization of clinical isolates of E. faecium[45]. According to our PFGE analysis, the 12 VREF isolates showed a heterogeneous pattern associated with a profile of multidrug resistance to different antibiotics and the presence of the vanA gene. The data obtained through PFGE revealed four clusters (I-IV), with a low similarity of 44% being detected among the VREF isolates and therefore high diversity.