| Accession | ARO:3004993 |
| CARD Short Name | Mtub_Rv3169_PZA |
| Definition | Mutations in the Rv3169 gene that can contribute to or confer resistance to pyrazinamide resistance. |
| AMR Gene Family | pyrazinamide resistant Rv3169 |
| Drug Class | pyrazine antibiotic |
| Resistance Mechanism | antibiotic target alteration |
| Classification | 9 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 Rv3169 + pyrazine antibiotic [Drug Class] |
| Parent Term(s) | 2 ontology terms | Show + pyrazinamide resistant Rv3169 [AMR Gene Family] + confers_resistance_to_antibiotic pyrazinamide [Antibiotic] |
| Publications | Sheen P, et al. 2017. BMC Genomics 18(1):769 A multiple genome analysis of Mycobacterium tuberculosis reveals specific novel genes and mutations associated with pyrazinamide resistance. (PMID 29020922) |
Prevalence of Mycobacterium tuberculosis Rv3169 mutations confer resistance to pyrazinamide 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 |
|---|---|---|---|---|
| No prevalence data | ||||
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): 680
Legend:
Published Variants:
PMID in progress (TB): N56S W171R A190G A194P Y53STOP
ReSeqTB:
| High Confidence | W171R |
| Minimal Confidence | Y53STOP N56S A190G A194P |