Abstract
To characterize the relationship between penicillin-binding protein 2 (PBP2/penA) and susceptibility to extended-spectrum cephalosporins (ESCs) and carbapenem antibiotics, we compared 17 PBP2 variants in Neisseria gonorrhoeae. Nonmosaic and mosaic variants of PBP2 caused decreased susceptibility to ESCs and, to a lesser extent, to carbapenems. An A501P substitution in mosaic XXXIV_A501P conferred decreased susceptibility to ESCs but restored carbapenem susceptibility to wild-type levels. These results could aid the molecular surveillance of antimicrobial resistance to these agents.
Copyright © 2015, American Society for Microbiology. All Rights Reserved.
MeSH terms
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Anti-Bacterial Agents / pharmacology
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Carbapenems / pharmacology*
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Carrier Proteins / genetics*
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Cephalosporins / pharmacology*
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Drug Resistance, Multiple, Bacterial / genetics
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Genetic Variation
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Gonorrhea / drug therapy
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Humans
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Microbial Sensitivity Tests
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Molecular Sequence Data
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Neisseria gonorrhoeae / drug effects*
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Neisseria gonorrhoeae / genetics*
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Neisseria gonorrhoeae / isolation & purification
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Serine-Type D-Ala-D-Ala Carboxypeptidase
Substances
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Anti-Bacterial Agents
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Carbapenems
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Carrier Proteins
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Cephalosporins
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Serine-Type D-Ala-D-Ala Carboxypeptidase
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penicillin-binding protein 2, Neisseria gonorrhoeae
Associated data
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GENBANK/KP721215
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GENBANK/KP721216
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GENBANK/KP721217
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GENBANK/KP721218
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GENBANK/KP721219