A novel VIM-type metallo-β-lactamase variant, VIM-60, was identified in multidrug-resistant clinical isolates in Japan. Compared with VIM-2, VIM-60 had two amino acid substitutions (Arg228Leu and His252Arg) and higher catalytic activities against fourth-generation cephalosporins. The genetic context for was - on the chromosome.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6535569PMC
http://dx.doi.org/10.1128/AAC.00124-19DOI Listing

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