A total of 87 Acinetobacter baumannii nonrepetitive consecutive clinical isolates were tested for the presence of metallo--lactamases (MBLs). Results of phenotypic assays (MBL Etest, imipenem/imipenem-EDTA combined-disk test, and imipenem/EDTA double-disk synergy test) were negative in all cases, but molecular testing revealed the presence of two bla VIM-1 -carrying isolates. One isolate had bla VIM-1 preceded by a weak P1 promoter, and both had inactivated P2 promoters and reduced bla VIM-1 expression, partially justifying the results revealing hidden MBL phenotypes.Carbapenem-resistant Acinetobacter baumannii strains are increasingly recovered from hospitalized patients worldwide and in some cases are associated with high morbidity and mortality rates (5). Mechanisms of resistance in such strains have been associated with decreased permeability, efflux pump overexpression, and, more lately, production of carbapenemases (10). Metallo--lactamases (MBLs), mainly of types IMP and VIM, are increasingly associated with the reduced susceptibility to carbapenems seen in several gram-negative species (15). However, despite the worldwide occurrence of epidemic carbapenem-resistant strains, MBL-producing A. baumannii isolates have been found to be disseminated only in specific geographic areas (8, 10). In Greek hospitals high rates of carbapenem-resistant A. baumannii clinical isolates are also detected, but MBL producers have been recognized in only a few instances (12). Therefore, the detection of these enzymes is of major importance in the control of A. baumannii hospital infections.Several schemes have been proposed for the phenotypic detection of MBL-producing gram-negative species, including A. baumannii. These tests take advantage of the zinc dependence of MBLs by using chelating agents, such as EDTA, to inhibit enzyme activity (8). However, the phenotypic appearance of MBL-carrying organisms seems to depend on the nature of the bacterial host, since carbapenem-susceptible Enterobacteriaceae organisms may carry MBL genes not readily detectable by conventional assays (15). A recent study introduced a more sensitive procedure for MBL detection in a broad range of host organisms, including carbapenem-susceptible isolates (3). This prompted us to test a series of Greek A. baumannii clinical isolates which appeared to be MBL negative in routine clinical testing.The study included 87 A. baumannii clinical isolates consecutively recovered from separate patients during October 2006 to March 2007 at the University Hospital of Larissa, Larissa, Greece. Species identification was performed by use of an API 20NE system (bioMerieux, Marcy l'Etoile, France) and PCR amplification of the intrinsic bla OXA-51 allele (13). Imipenem and meropenem MICs were tested by the agar dilution method according to CLSI recommendations and interpretive criteria (1), while status of susceptibility to other -lactams, as well as to aminoglycosides, quinolones, and colistin, was investigated by disk diffusion testing. Pseudomonas aeruginosa A...