We describe here a non-O1/non-O139 Vibrio cholerae isolate producing both VIM-1 and VIM-4 carbapenemases. It was isolated from a yellow-legged gull in southern France. The bla VIM genes were part of a class 1 integron structure located in an IncA/C plasmid. This study emphasizes the presence of carbapenemase genes in wildlife microbiota.
Multidrug-resistant Vibrio cholerae strains have been increasingly reported worldwide (1). However, data on resistance to third-generation cephalosporins, mostly via genes encoding extended-spectrum -lactamase (ESBL) (2, 3) or cephalosporinase determinants (4) are limited. Carbapenemase-mediated resistance in Vibrio spp. has been reported only in India, where clinical and environmental V. cholerae isolates carrying the NDM-1 metalloenzyme were described in several studies (4-6). We describe here an avian strain of V. cholerae that was isolated in southern France and that coharbors the bla VIM-1 and bla VIM-4 carbapenemase genes.In April 2013, 93 cloacal swab samples from juvenile unfledged yellow-legged gulls (Larus michahellis) breeding on the island of Carteau, Port-Saint-Louis, France, were screened for bacteria resistant to broad-spectrum -lactam antibiotics. Briefly, swab samples were inoculated in Trypticase soy broth (Thermo Fisher Scientific) and grown at 37°C for 24 h. Samples were then subcultured in ESBL agar plates (bioMérieux, Marcy l'Etoile, France) and were examined after 24 and 48 h of incubation. Enterobacteriaceae resistant to multiple drugs via different resistance mechanisms (e.g., third-generation cephalosporin-resistant Escherichia coli and Proteus mirabilis harboring plasmid-mediated cephalosporinase genes or ESBL genes) were recovered (7; our unpublished data). In addition, a V. cholerae strain showing resistance to third-generation cephalosporins was detected. No other multidrug-resistant V. cholerae strain was recovered. Species identification was performed by matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) mass spectrometry (Bruker Daltonics, Bremen, Germany). Moreover, PCR analysis of the rfb gene cluster (8), the cholera toxin ctxA gene (9), and the colonization factor tcpA gene (9) revealed a nontoxigenic, non-O1/non-O139 isolate.Susceptibility testing was performed using the disk diffusion method on Mueller-Hinton agar and was interpreted according to the European Committee on Antimicrobial Susceptibility Testing (EUCAST) clinical breakpoints (version 5.0) (http://www.eucast .org/clinical_breakpoints/) (10). The strain was intermediate or resistant to most -lactam antibiotics, except aztreonam. The MICs for amoxicillin, cefotaxime, ceftazidime, imipenem, ertapenem, doripenem, and meropenem were determined in the parental strain and the transconjugant with the Etest method (bioMérieux, Marcy l'Etoile, France) ( Table 1). Metallo--lactamase production was observed by using the carbapenemase/metallo--lactamase confirmative identification pack (Rosco Diagnostica NeoSensitabs, Eurobio, Courtaboeuf, France). Specifically, redu...