| Accession | ARO:3002272 |
| CARD Short Name | VIM-2 |
| Definition | VIM-2 is a beta-lactamase found in Pseudomonas spp. |
| AMR Gene Family | VIM beta-lactamase |
| Drug Class | penem, penam, cephamycin, cephalosporin, carbapenem |
| Resistance Mechanism | antibiotic inactivation |
| Resistomes with Perfect Matches | Acinetobacter pittiip, Alcaligenes faecaliswgs, Citrobacter freundiiwgs, Enterobacter asburiaewgs, Enterobacter hormaecheiwgs, Escherichia coliwgs, Klebsiella pneumoniaewgs, Providencia rettgeriwgs, Pseudomonas aeruginosag+p+wgs+gi, Pseudomonas chlororaphiswgs, Pseudomonas monteiliig+wgs, Pseudomonas putidag+p+wgs, Pseudomonas stutzerig+p+wgs, Serratia marcescenswgs |
| Resistomes with Sequence Variants | Acinetobacter pittiip, Alcaligenes faecaliswgs, Citrobacter freundiiwgs, Enterobacter asburiaewgs, Enterobacter hormaecheiwgs, Escherichia coliwgs, Klebsiella pneumoniaewgs, Providencia rettgeriwgs, Pseudomonas aeruginosag+p+wgs+gi, Pseudomonas chlororaphiswgs, Pseudomonas monteiliig+wgs, Pseudomonas putidag+p+wgs, Pseudomonas stutzerig+p+wgs, Serratia marcescenswgs |
| Classification | 18 ontology terms | Show + process or component of antibiotic biology or chemistry + mechanism of antibiotic resistance + determinant of antibiotic resistance + antibiotic inactivation [Resistance Mechanism] + antibiotic inactivation enzyme + hydrolysis of antibiotic conferring resistance + antibiotic molecule + hydrolysis of beta-lactam antibiotic by metallo-beta-lactamase + beta-lactam antibiotic + beta-lactamase + cephem + class B (metallo-) beta-lactamase + penem [Drug Class] + subclass B1 (metallo-) beta-lactamase + penam [Drug Class] + cephamycin [Drug Class] + cephalosporin [Drug Class] + carbapenem [Drug Class] |
| Parent Term(s) | 1 ontology terms | Show + VIM beta-lactamase [AMR Gene Family] |
| Sub-Term(s) | 8 ontology terms | Show + taniborbactam [Adjuvant] is_small_molecule_inhibitor + bispicen [Adjuvant] is_small_molecule_inhibitor + trispicen [Adjuvant] is_small_molecule_inhibitor + trispicen A [Adjuvant] is_small_molecule_inhibitor + aspergillomarasmine A [Adjuvant] is_small_molecule_inhibitor + unithiol [Adjuvant] is_small_molecule_inhibitor + ANT-431 [Adjuvant] is_small_molecule_inhibitor + ME1071 [Adjuvant] is_small_molecule_inhibitor |
| Publications | Poirel L, et al. 2000. Antimicrob Agents Chemother 44(4): 891-897. Characterization of VIM-2, a carbapenem-hydrolyzing metallo-beta-lactamase and its plasmid- and integron-borne gene from a Pseudomonas aeruginosa clinical isolate in France. (PMID 10722487) |
Prevalence of VIM-2 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 |
|---|---|---|---|---|
| Acinetobacter pittii | 0% | 0.99% | 0% | 0% |
| Alcaligenes faecalis | 0% | 0% | 8.82% | 0% |
| Citrobacter freundii | 0% | 0% | 0.58% | 0% |
| Enterobacter asburiae | 0% | 0% | 0.79% | 0% |
| Enterobacter hormaechei | 0% | 0% | 0.04% | 0% |
| Escherichia coli | 0% | 0% | 0.01% | 0% |
| Klebsiella pneumoniae | 0% | 0% | 0.02% | 0% |
| Providencia rettgeri | 0% | 0% | 1.27% | 0% |
| Pseudomonas aeruginosa | 3.22% | 1.17% | 3.5% | 9.72% |
| Pseudomonas chlororaphis | 0% | 0% | 1.61% | 0% |
| Pseudomonas monteilii | 22.22% | 0% | 7.14% | 0% |
| Pseudomonas putida | 1.41% | 4% | 3.74% | 0% |
| Pseudomonas stutzeri | 3.57% | 9.09% | 5.34% | 0% |
| Serratia marcescens | 0% | 0% | 0.52% | 0% |
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): 400
