Browse AMR Genes
Explore antimicrobial resistance genes from the literature
Explore antimicrobial resistance genes from the literature
DNA repair enzyme
Overview
| Protein Change | Nucleotide Change | Mechanism | Organism | Resistance To | Database | Validation Status |
|---|---|---|---|---|---|---|
| A422S | - | - | E. coli | ciprofloxacinfluoroquinolones | Reslit | Candidate |
Antibiotic resistance in Pseudomonas aeruginosa strains with increased mutation frequency due to inactivation of the DNA oxidative repair system.
Inactivation of the DNA oxidative repair system genes mutT, mutY, and mutM in Pseudomonas aeruginosa leads to increased mutation frequency and antibiotic resistance, primarily through increased β-lactamase production and overexpression of the MexCD-OprJ efflux pump.
Novel Conserved Genotypes Correspond to Antibiotic Resistance Phenotypes of E. coli Clinical Isolates.
The study identifies novel SNPs in gyrA, mutM, ligB, and recG genes associated with fluoroquinolone resistance in E. coli clinical isolates, demonstrating their role in resistance mechanisms through experimental validation.
Pseudomonas aeruginosa heteroresistance to levofloxacin caused by upregulated expression of essential genes for DNA replication and repair.
The study identifies that upregulated expression of genes involved in DNA replication and repair, such as recA, uvrD, xseB, ssb, mutM, and crc, contributes to levofloxacin heteroresistance in Pseudomonas aeruginosa strains PAS71 and PAS81. Additionally, the expression of genes related to bacterial secretion systems, such as gspD, vgrG1, hcpC, clpV1, and ppkA, is increased in PAS81 under LVX stress.
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