bla OXA-23 was not detected in most (17/21) isolates of the novel STs. This phenomenon was also present in this study as all the local carbapenem-resistant isolates Rigosertib purchase carrying bla OXA-23 belonged to CC92. It has been suggested that among carbapenem-resistant isolates some belonging to certain clonal complexes appeared to be more successful [12–14]. The diversity of A. Selinexor in vivo baumannii isolates in our settings could provide useful information for infection control. The clonal diversity of A. baumannii

and the fact that carbapenem resistance could be transmitted horizontally highlight that “horizontal” infection control measures such as environmental cleaning and hand hygiene should be reinforced to reduce the further spread of A. baumannii. Person-to-person transmission of carbapenem-non-susceptible A. baumannii carrying bla OXA-23 was indeed identified for several cases as evidenced by the fact that isolates recovered from different patients belonged to the same pulsotype (Table 1

and Figure 1). This suggests that effective infection control measures might need to include rapid identification of bla OXA-23 by molecular methods and also justifies contact precautions for patients with carbapenem-resistant isolates. Conclusions This study provided a snapshot of A. baumannii population in clinical samples in our local settings. Significantly diverse clonal origins were identified but most isolates belonged to the globally-distributed CC92. Among CC92, ST75, ST92 and ST208 were the most common types in our region. The high prevalence of ST208 carrying bla OXA-23 suggests that ST208 selleck chemicals llc appears to be an emerging lineage mediating the spread of carbapenem resistance. The diversity of A. baumannii suggested that the current MLST scheme might need to be further optimized and in particular the gpi gene might not be an ideal target for Acinetobacter MLST. Methods Strains The study included Anidulafungin (LY303366) all non-repetitive isolates (n = 82) that were recovered from clinical specimens from June 22 to June 25, 2011 in 13 hospitals in Sichuan, southwest China and were putatively

identified as A. baumannii or belonging to the Acinetobacter calcoaceticus-baumannii complex using the Vitek II, MicroScan and Phoenix automated systems. The clinical samples were taken as part of standard patient care and therefore no ethical approval was applied for their use. The 13 hospitals are all tertiary with 19,051 beds in total (ranged from 800 to 4,300) including 3 university hospitals and 10 municipal ones. For each patient, only one isolate was collected. Genomic species identification was established by partially sequencing the recA gene as described previously [15]. In vitro susceptibility test MICs of meropenem, imipenem, ceftazidime, sulbactam, minocycline, polymyxin, ciprofloxacin, rifampicin and cotrimoxazole against A.