Accession | ARO:3004083 |
CARD Short Name | AcrEF_TolC_CIP |
Definition | AcrEF-TolC efflux pump system of E. coli confers resistance to fluoroquinolones (ciprofloxacin). |
AMR Gene Family | resistance-nodulation-cell division (RND) antibiotic efflux pump |
Drug Class | penam, cephamycin, cephalosporin, fluoroquinolone antibiotic |
Resistance Mechanism | antibiotic efflux |
Efflux Component | efflux pump complex or subunit conferring antibiotic resistance |
Classification | 13 ontology terms | Show + process or component of antibiotic biology or chemistry + antibiotic molecule + mechanism of antibiotic resistance + beta-lactam antibiotic + determinant of antibiotic resistance + antibiotic efflux [Resistance Mechanism] + cephem + efflux pump complex or subunit conferring antibiotic resistance [Efflux Component] + penam [Drug Class] + resistance-nodulation-cell division (RND) antibiotic efflux pump [AMR Gene Family] + cephamycin [Drug Class] + cephalosporin [Drug Class] + fluoroquinolone antibiotic [Drug Class] |
Parent Term(s) | 2 ontology terms | Show |
Sub-Term(s) | 5 ontology terms | Show |
Publications | Lau SY and Zgurskaya HI. 2005. J Bacteriol 187(22): 7815-7825. Cell division defects in Escherichia coli deficient in the multidrug efflux transporter AcrEF-TolC. (PMID 16267305) Poole K, et al. 2000. Antimicrob. Agents Chemother. 44(9):2233-41 Efflux-mediated resistance to fluoroquinolones in gram-negative bacteria. (PMID 10952561) |
Prevalence of AcrEF-TolC confers resistance to ciprofloxacin among the sequenced genomes, plasmids, and whole-genome shotgun assemblies available at NCBI or IslandViewer for 413 important pathogens (see methodological details and complete list of analyzed pathogens). Values reflect percentage of genomes, plasmids, genome islands, or whole-genome shotgun assemblies that have at least one hit to the AMR detection model. Default view includes percentages calculated based on Perfect plus Strict RGI hits. Select the checkbox to view percentages based on only Perfect matches to AMR reference sequences curated in CARD (note: this excludes resistance via mutation as references in protein variant models are often wild-type, sensitive sequences).
Species | NCBI Chromosome | NCBI Plasmid | NCBI WGS | NCBI GI |
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No prevalence data | ||||