CDA-1

Accession ARO:3007650
CARD Short NameCDA-1
DefinitionCDA-1 was recovered from a urine sample and is intermediate or resistant to third-generation cephalosporins and carbapenems. Susceptibility testing, isoelectric focusing, and analysis of outer membrane proteins showed that AmpC beta-lactamase expression combined with porin deficiency accounted for the carbapenem resistance.
AMR Gene FamilyCDA beta-lactamase
Drug Classpenicillin beta-lactam, cephalosporin, carbapenem
Resistance Mechanismantibiotic inactivation
Classification25 ontology terms | Show
Parent Term(s)6 ontology terms | Show
+ confers_resistance_to_antibiotic cefoxitin [Antibiotic]
+ confers_resistance_to_antibiotic cefalotin [Antibiotic]
+ confers_resistance_to_antibiotic ticarcillin [Antibiotic]
+ confers_resistance_to_antibiotic ticarcillin-clavulanic acid [Antibiotic+Adjuvant]
+ confers_resistance_to_antibiotic cephaloridine [Antibiotic]
+ CDA beta-lactamase [AMR Gene Family]
Publications

Ammenouche N, et al. 2014. Antimicrob Agents Chemother 58(11):6942-5 Characterization of a novel AmpC β-lactamase produced by a carbapenem-resistant Cedecea davisae clinical isolate. (PMID 25136020)

Resistomes

Prevalence of CDA-1 among the sequenced genomes, plasmids, and whole-genome shotgun assemblies available at NCBI or IslandViewer for 414 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).

Prevalence: protein homolog model

SpeciesNCBI ChromosomeNCBI PlasmidNCBI WGSNCBI GIGRDI-AMR2
No prevalence data


Detection Models

Model Type: protein homolog model

Model Definition: Protein Homolog Models (PHM) detect protein sequences based on their similarity to a curated reference sequence, using curated BLASTP bitscore cut-offs. Protein Homolog Models apply to all genes that confer resistance through their presence in an organism, such as the presence of a beta-lactamase gene on a plasmid. PHMs include a reference sequence and a bitscore cut-off for detection using BLASTP. A Perfect RGI match is 100% identical to the reference protein sequence along its entire length, a Strict RGI match is not identical but the bit-score of the matched sequence is greater than the curated BLASTP bit-score cutoff, Loose RGI matches have a bit-score less than the curated BLASTP bit-score cut-off.

Bit-score Cut-off (blastP): 700


>gb|AID52933.1|+|CDA-1 [Cedecea davisae]
MKKSLCLTLLLAASCSTFAAPKQLTAQQIEKIVNRTISPLLKEQAIPGMAVAVIYKGYPLYFTWGKADVQHNEPVTRQTLFELGSVSKTF
TGVLGGDTLARGEISLSDPAQKYWPELTGSQWKGITLLQLATYTAGGLPLQVPDEVTDSASLLNFYQSWQPQWAPGSKRLYANASIGLFG
ALMVKPSGMGFEQAMTTRVLEPLKLAHTWITVPPAEESHYAWGYRNDKAVRVSPGMLDAEAYGVKSSIEDMAHWVQANMVPERVEDQNLQ
QGIKLAQSRYWRIGSMYQGLGWEMLNWPLKGKVIIDGSDNKVALAPQTAVAIDPPAPLVKASWVHKTGSTGGFGSYVAFIPEKQLGIVML
ANKSYPNPERVKAAYAILEALQ


>gb|KJ650399.1|+|1-1149|CDA-1 [Cedecea davisae]
ATGAAAAAATCCCTCTGCCTGACGCTGCTGCTCGCCGCCTCATGCTCTACTTTTGCCGCGCCAAAGCAGCTTACCGCGCAGCAGATCGAA
AAAATCGTTAATCGCACGATTTCGCCGCTGCTGAAAGAGCAGGCGATCCCGGGTATGGCAGTCGCCGTTATCTATAAAGGCTACCCGCTG
TATTTCACCTGGGGCAAAGCCGACGTGCAGCATAACGAACCGGTAACCCGGCAAACTCTGTTCGAGCTTGGTTCTGTAAGTAAAACATTT
ACCGGCGTGCTGGGCGGGGATACGCTGGCTCGCGGCGAGATAAGCCTTAGCGATCCGGCGCAAAAATATTGGCCAGAGCTAACCGGCAGC
CAGTGGAAAGGAATAACGCTATTGCAACTGGCAACCTATACAGCAGGCGGGTTGCCGCTACAGGTGCCTGATGAAGTTACCGACAGCGCC
TCGCTGCTCAACTTTTACCAGTCATGGCAGCCGCAGTGGGCACCAGGCAGCAAAAGGCTCTATGCCAACGCCAGCATTGGGTTGTTTGGG
GCGTTGATGGTTAAGCCTTCAGGAATGGGCTTCGAGCAGGCGATGACAACGCGAGTGCTGGAACCATTGAAGCTGGCTCATACCTGGATA
ACCGTTCCTCCCGCTGAAGAGAGCCATTACGCCTGGGGCTACCGCAACGACAAAGCGGTACGCGTTTCACCGGGCATGCTGGATGCAGAA
GCCTACGGCGTTAAGTCCAGCATCGAAGATATGGCGCACTGGGTGCAGGCGAATATGGTGCCGGAGCGGGTGGAAGACCAAAATCTGCAA
CAGGGGATCAAACTTGCTCAGTCTCGCTACTGGCGGATTGGCAGCATGTATCAGGGTCTGGGCTGGGAAATGCTGAACTGGCCGCTGAAG
GGCAAAGTGATTATCGACGGCAGCGATAATAAAGTCGCCCTTGCCCCGCAGACCGCGGTCGCTATTGACCCACCGGCCCCGCTAGTGAAG
GCATCCTGGGTACACAAAACTGGCTCAACCGGCGGCTTCGGTAGCTATGTGGCCTTTATTCCCGAAAAGCAGTTGGGCATCGTGATGCTG
GCGAACAAAAGCTACCCGAATCCTGAGCGGGTAAAAGCCGCCTACGCTATTCTCGAAGCGCTGCAATAA

Curator Acknowledgements
Curator Description Most Recent Edit