Browse AMR Genes
Explore antimicrobial resistance genes from the literature
Explore antimicrobial resistance genes from the literature
efflux pump component
Overview
| Protein Change | Nucleotide Change | Mechanism | Organism | Resistance To | Database | Validation Status |
|---|---|---|---|---|---|---|
| Q178R | - | multidrug efflux RND transporter permease subunit MexD | Pseudomonas aeruginosa | Ceftolozane/tazobactam|Ceftazidime-avibactamAVIBACTAM | Reference Gene CatalogReslit | Confirmed |
| S133G | - | multidrug efflux RND transporter permease subunit MexD | Pseudomonas aeruginosa | Ceftolozane/tazobactam|Ceftazidime-avibactamAVIBACTAM | Reference Gene CatalogReslit | Confirmed |
| T87S | - | - | Pseudomonas aeruginosa | Levofloxacin | Reslit | Candidate |
| F608C | - | - | Pseudomonas aeruginosa | Tigecycline | Reslit | Candidate |
| P809A | - | - | Pseudomonas aeruginosa | Ciprofloxacin|Norfloxacin|Imipenem|Meropenem | Reslit | Candidate |
| G195D | - | - | Pseudomonas aeruginosa | Piperacillin/tazobactam|Ceftazidime|Cefepime|Meropenem|Imipenem|Tobramycin|Ciprofloxacin | Reslit | Candidate |
Evolution of Pseudomonas aeruginosa Antimicrobial Resistance and Fitness under Low and High Mutation Rates.
Genomics and Susceptibility Profiles of Extensively Drug-Resistant Pseudomonas aeruginosa Isolates from Spain.
The study identified various AMR genes and mutations in extensively drug-resistant Pseudomonas aeruginosa isolates from Spain, including beta-lactamases, aminoglycoside-modifying enzymes, and mutations in genes such as ampC, oprD, gyrA, parC, mexZ, and glpT, which contribute to resistance against multiple antibiotics.
Application of six multiplex PCR's among 200 clinical isolates of Pseudomonas aeruginosa for the detection of 20 drug resistance encoding genes.
The study identified several beta-lactamase genes (blaTem, blaOXA, blaCTX-M-15, blaVim, blaGes, blaVeb, blaDIM, AmpC) and efflux pump genes (MexA, MexB, OprM, MexC, MexD, OprJ, MexX, MexY, OprN, nfxB, MexR, OprD) in Pseudomonas aeruginosa clinical isolates, highlighting their roles in mediating resistance to various antibiotics.
Transcriptome Analysis Reveals the Resistance Mechanism of Pseudomonas aeruginosa to Tachyplesin I.
The study identifies several efflux pump genes, including mexB, mexC, mexR, armR, and others, that are upregulated in tachyplesin I-resistant Pseudomonas aeruginosa strains, suggesting their role in resistance through increased efflux of the antimicrobial peptide.
Full pathogen characterisation: species identification including the detection of virulence factors and antibiotic resistance genes via multiplex DNA-assays.
The study presents a DNA microarray-based assay for the simultaneous detection of 44 sepsis-relevant bacterial pathogens, 360 virulence factors, and 409 antibiotic resistance genes. The assay was evaluated with 14 multidrug-resistant strains, including all ESKAPE pathogens.
Emergence of Resistance to Novel Cephalosporin–β-Lactamase Inhibitor Combinations through the Modification of the Pseudomonas aeruginosa MexCD-OprJ Efflux Pump.
The study identified mutations in the mexD gene of Pseudomonas aeruginosa that modify the substrate specificity of the MexCD-OprJ efflux pump, leading to resistance against ceftolozane-tazobactam and ceftazidime-avibactam.
Combination of phage therapy and cefiderocol to successfully treat Pseudomonas aeruginosa cranial osteomyelitis.
The study identifies the presence of the blaGES-1 gene and MDR efflux pumps MexD and MexX in multidrug-resistant P. aeruginosa isolates, which contribute to resistance against various β-lactam antibiotics. Phage therapy in combination with cefiderocol was successful in treating the infection.
Antibiotic resistance in plant growth promoting bacteria: A comprehensive review and future perspectives to mitigate potential gene invasion risks.
This review highlights the prevalence of antibiotic resistance genes (ARGs) in plant growth-promoting bacteria (PGPB) and emphasizes the potential risks of ARG dissemination through biofertilizers. Key findings include the identification of various ARGs such as bacA, fosB, ermD, bl2a, vanSA, cat, acrD, mexF, mexD, mexW, mexE, mexY, mexX, mexZ, mexR, mexA, mexB, mexC, mexD, mexE, and mexF, which confer resistance to multiple antibiotics.
Genomic analysis of multidrug-resistant Delftia tsuruhatensis isolated from raw bovine milk.
The study identifies multiple efflux pump genes and a genus-specific OXA-926-like beta-lactamase in the multidrug-resistant Delftia tsuruhatensis strain MR-6/3H, contributing to resistance against various antibiotics.
Bacterial diversity and resistome analysis of drinking water stored in cisterns from two First Nations communities in Manitoba, Canada.
The study identified a diverse array of antimicrobial resistance genes in drinking water stored in cisterns from two First Nations communities in Manitoba, Canada. Key findings include the presence of genes such as aac(3')-Ia, aac(6')-Iia, aac(6')-Iic, aph(3')-Ia, acrD, smeB, smeR, FEZ-1, rm3, SPG-1, OXA-21, OXA-119, OXA-205, dfrA14, dfrB6, acrB, acrF, adeF, ceoB, emrA, mexE, mexF, mexI, oprN, oqxB, BRP(MBL), vanSO, axyY, CRP, efrB, macB, mexB, mexC, mexD, mexK, mexQ, mexW, mexY, mtrA, muxB, muxC, oleB, oleC, ompB, oprM, smeD, smeE, golS, mdsB, PER-2, TEM-126, msbA, arnA, bacA, bcrA, MCR-5, rosA, rosB, rpoB2, ugd, mexN, taeA, efpA, rphA, rphB, otr(A), otrC, tetA(48 ), ompH, and triC, which confer resistance to various antibiotics including aminoglycosides, beta-lactams, cephalosporins, carbapenems, fluoroquinolones, macrolides, monobactams, nitroimidazoles, peptides, phenicols, pleuromutilins, rifamycins, tetracyclines, and triclosan.
The mobilome landscape of biocide-resistance in Brazilian ESKAPE isolates.
The study identified multiple biocide resistance genes in Brazilian ESKAPE isolates, highlighting the presence of resistance mechanisms against benzalkonium chloride, chlorhexidine, and triclosan. Key genes included efflux pumps (acrE/envC, acrF/envD, adeA, adeB, adeC, mexD, oqxA, oqxB, qacA, qacR, sdeB), enzyme modifiers (fabV, sh-fabI), and porins (kpnO).
From Proteome to Potential Drugs: Integration of Subtractive Proteomics and Ensemble Docking for Drug Repurposing against Pseudomonas aeruginosa RND Superfamily Proteins.
The study identifies and characterizes essential proteins in Pseudomonas aeruginosa, particularly RND efflux pumps, which are critical for antibiotic resistance. Computational methods and ensemble docking were used to find potential inhibitors like MK-3207, R-428, and Suramin, showing promise for drug repurposing.
Ciprofloxacin resistance rapidly declines in nfxB defective clinical strains of Pseudomonas aeruginosa.
The study demonstrates that ciprofloxacin resistance in nfxB-defective Pseudomonas aeruginosa clinical strains can rapidly decline in antibiotic-free environments due to compensatory mutations in the mexCD-oprJ operon, particularly in mexC and mexD genes.
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