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Class A carbapenemase FPH-1 from Francisella philomiragia.


ABSTRACT: FPH-1 is a new class A carbapenemase from Francisella philomiragia. It produces high-level resistance to penicillins and the narrow-spectrum cephalosporin cephalothin and hydrolyzes these ?-lactam antibiotics with catalytic efficiencies of 10(6) to 10(7) M(-1) s(-1). When expressed in Escherichia coli, the enzyme confers resistance to clavulanic acid, tazobactam, and sulbactam and has K(i) values of 7.5, 4, and 220 ?M, respectively, against these inhibitors. FPH-1 increases the MIC of the monobactam aztreonam 256-fold and the MIC of the broad-spectrum cephalosporin ceftazidime 128-fold, while the MIC of cefoxitin remains unchanged. MICs of the carbapenem antibiotics imipenem, meropenem, doripenem, and ertapenem are elevated 8-, 8-, 16-, and 64-fold, respectively, against an E. coli JM83 strain producing the FPH-1 carbapenemase. The catalytic efficiencies of the enzyme against carbapenems are in the range of 10(4) to 10(5) M(-1) s(-1). FPH-1 is 77% identical to the FTU-1 ?-lactamase from Francisella tularensis and has low amino acid sequence identity with other class A ?-lactamases. Together with FTU-1, FPH-1 constitutes a new branch of the prolific and ever-expanding class A ?-lactamase tree.

SUBMITTER: Toth M 

PROVIDER: S-EPMC3370778 | biostudies-literature | 2012 Jun

REPOSITORIES: biostudies-literature

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Class A carbapenemase FPH-1 from Francisella philomiragia.

Toth Marta M   Vakulenko Viktoria V   Antunes Nuno T NT   Frase Hilary H   Vakulenko Sergei B SB  

Antimicrobial agents and chemotherapy 20120326 6


FPH-1 is a new class A carbapenemase from Francisella philomiragia. It produces high-level resistance to penicillins and the narrow-spectrum cephalosporin cephalothin and hydrolyzes these β-lactam antibiotics with catalytic efficiencies of 10(6) to 10(7) M(-1) s(-1). When expressed in Escherichia coli, the enzyme confers resistance to clavulanic acid, tazobactam, and sulbactam and has K(i) values of 7.5, 4, and 220 μM, respectively, against these inhibitors. FPH-1 increases the MIC of the monoba  ...[more]

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