| Accession | ARO:3003301 |
| CARD Short Name | Saur_gyrB_AMU |
| Definition | Point mutation in Staphylococcus aureus resulting in aminocoumarin resistance. |
| AMR Gene Family | aminocoumarin resistant gyrB |
| Drug Class | aminocoumarin antibiotic |
| Resistance Mechanism | antibiotic target alteration |
| Resistomes with Sequence Variants | Staphylococcus aureuswgs, Staphylococcus capitisg+wgs, Staphylococcus epidermidisg+p+wgs, Staphylococcus pasteurig+wgs, Staphylococcus warnerig+wgs |
| Classification | 10 ontology terms | Show + process or component of antibiotic biology or chemistry + mechanism of antibiotic resistance + antibiotic target alteration [Resistance Mechanism] + mutation conferring antibiotic resistance + determinant of antibiotic resistance + antibiotic resistant gene variant or mutant + antibiotic molecule + antibiotic resistant DNA topoisomerase subunit + antibiotic resistant DNA topoisomerase subunit gyrB + aminocoumarin antibiotic [Drug Class] |
| Parent Term(s) | 4 ontology terms | Show + aminocoumarin resistant gyrB [AMR Gene Family] + confers_resistance_to_antibiotic novobiocin [Antibiotic] + confers_resistance_to_antibiotic clorobiocin [Antibiotic] + confers_resistance_to_antibiotic coumermycin A1 [Antibiotic] |
| Publications | Fujimoto-Nakamura M, et al. 2005. Antimicrob Agents Chemother 49(9): 3810-3815. Accumulation of mutations in both gyrB and parE genes is associated with high-level resistance to novobiocin in Staphylococcus aureus. (PMID 16127057) |
Prevalence of Staphylococcus aureus gyrB conferring resistance to aminocoumarin 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 |
|---|---|---|---|---|
| Staphylococcus aureus | 0% | 0% | 0.02% | 0% |
| Staphylococcus capitis | 100% | 0% | 68.99% | 0% |
| Staphylococcus epidermidis | 88.39% | 0.29% | 68.03% | 0% |
| Staphylococcus pasteuri | 12.5% | 0% | 3.85% | 0% |
| Staphylococcus warneri | 100% | 0% | 73.77% | 0% |
Model Type: protein variant model
Model Definition: Protein Variant Models (PVM) perform a similar search as Protein Homolog Models (PHM), i.e. detect protein sequences based on their similarity to a curated reference sequence, but secondarily screen query sequences for curated sets of mutations to differentiate them from antibiotic susceptible wild-type alleles. PVMs are designed to detect AMR acquired via mutation of house-keeping genes or antibiotic targets, e.g. a mutated gyrase resistant to aminocoumarin antibiotics. PVMs include a protein reference sequence (often from antibiotic susceptible wild-type alleles), a curated bit-score cut-off, and mapped resistance variants. Mapped resistance variants may include any or all of single point mutations, insertions, or deletions curated from the scientific literature. A Strict RGI match has a BLASTP bit-score above the curated BLASTP cutoff value and contains at least one curated mutation from amongst the mapped resistance variants, while a Loose RGI match has a bit-score less than the curated BLASTP bit-score cut-off but still contains at least one curated mutation from amongst the mapped resistance variants.
Bit-score Cut-off (blastP): 1200
Legend:
Published Variants:
| PMID: 16127057 | I56S G85S I102S S128L R144S R144I T173A |