Browse AMR Genes
Explore antimicrobial resistance genes from the literature
Explore antimicrobial resistance genes from the literature
Murein recycling transporter
Overview
| Protein Change | Nucleotide Change | Mechanism | Organism | Resistance To | Database | Validation Status |
|---|---|---|---|---|---|---|
| Q131P | - | loss of function | Pseudomonas aeruginosa, Escherichia coli, Vibrio cholerae, Acinetobacter baumannii | Ampicillin | Reslit | Candidate |
| Q131R | - | loss of function | Escherichia coli, Vibrio cholerae, Pseudomonas aeruginosa, Acinetobacter baumannii | Ampicillin | Reslit | Candidate |
| Q131H | - | loss of function | Pseudomonas aeruginosa, Escherichia coli, Vibrio cholerae, Acinetobacter baumannii |
Reslit |
| Candidate |
| A197S | - | loss of function | Pseudomonas aeruginosa, Escherichia coli, Vibrio cholerae, Acinetobacter baumannii | Ampicillin | Reslit | Candidate |
| A197D | - | loss of function | Pseudomonas aeruginosa, Escherichia coli, Vibrio cholerae, Acinetobacter baumannii | Ampicillin | Reslit | Candidate |
| G29V | - | loss of function | Pseudomonas aeruginosa, Escherichia coli, Vibrio cholerae, Acinetobacter baumannii | Ampicillin | Reslit | Candidate |
| A129T | - | loss of function | Escherichia coli, Vibrio cholerae, Acinetobacter baumannii, Pseudomonas aeruginosa | Ampicillin | Reslit | Candidate |
| A129V | - | loss of function | Vibrio cholerae, Acinetobacter baumannii, Pseudomonas aeruginosa, Escherichia coli | Ampicillin | Reslit | Candidate |
| A129D | - | loss of function | Acinetobacter baumannii, Pseudomonas aeruginosa, Escherichia coli, Vibrio cholerae | Ampicillin | Reslit | Candidate |
| G29A | - | loss of function | Pseudomonas aeruginosa, Escherichia coli, Vibrio cholerae, Acinetobacter baumannii | Ampicillin | Reslit | Candidate |
| Q131E | - | loss of function | Pseudomonas aeruginosa, Escherichia coli, Vibrio cholerae, Acinetobacter baumannii | Ampicillin | Reslit | Candidate |
| I53T | - | drastically lowered | Pseudomonas aeruginosa | Ampicillin | Reslit | Candidate |
| W90R | - | no significant change | Pseudomonas aeruginosa | Ampicillin | Reslit | Candidate |
| I53S | - | drastically lowered | Pseudomonas aeruginosa | Ampicillin | Reslit | Candidate |
| W90S | - | no significant change | Pseudomonas aeruginosa | Ampicillin | Reslit | Candidate |
| A583T | - | - | Pseudomonas aeruginosa | Ceftazidime/avibactam | Reslit | Candidate |
Genetic architecture of intrinsic antibiotic susceptibility.
The study identifies multiple genes and mutations that contribute to antibiotic tolerance in E. coli, revealing a large mutational target size for increasing drug resistance. Key findings include the role of genes involved in electron transport, flagella synthesis, and efflux pumps in modulating susceptibility to various antibiotics.
The regulatory repertoire of Pseudomonas aeruginosa AmpC ß-lactamase regulator AmpR includes virulence genes.
AmpR is a global regulator in P. aeruginosa that influences the expression of over 500 genes, including those involved in β-lactam resistance, virulence, and biofilm formation.
Effect of β-lactam antibiotic resistance gene expression on the radio-resistance profile of E. coli O157:H7.
The study shows that the expression of ampC and ampG genes in E. coli O157:H7 contributes to radioresistance, particularly when the bacteria are adapted to carbenicillin. Mutants lacking these genes showed increased sensitivity to irradiation.
Synergism of imipenem with fosfomycin associated with the active cell wall recycling and heteroresistance in Acinetobacter calcoaceticus-baumannii complex.
The study identifies carbapenemase genes blaOXA-24, blaOXA-23, and blaOXA-58 along with blaIMP in various Acinetobacter isolates, contributing to carbapenem resistance. It also highlights the role of cell wall recycling pathways and heteroresistance in modulating the effectiveness of imipenem-fosfomycin synergy.
Mucilaginibacter sp. Strain Metal(loid) and Antibiotic Resistance Isolated from Estuarine Soil Contaminated Mine Tailing from the Fundão Dam.
The study identifies multiple AMR genes in Mucilaginibacter sp. 21p, including genes for resistance to quinolones, aminoglycosides, beta-lactamases, sulfonamides, tetracyclines, daptomycin, arsenic, zinc, manganese, cobalt, and cadmium. These genes are part of efflux pumps and other resistance mechanisms, indicating the strain's adaptability to metal(loid) and antibiotic stressors in contaminated environments.
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