Target intelligence / Profile preview

Antibiotic resistance gene (ARG)

Target
ARG
Molecular classification
Other, Nucleic acid, Genetic element
01

Overview

Antibiotic resistance genes (ARGs) are specific genetic sequences within bacteria that encode mechanisms to survive exposure to antimicrobial agents (NIH, 2023). These genes function by producing proteins that enzymatically degrade antibiotics (such as beta-lactamases), actively pump drugs out of the cell via efflux systems, or alter the antibiotic's cellular target to prevent binding (Nature Reviews Microbiology, 2021). ARGs are frequently located on mobile genetic elements like plasmids and transposons, facilitating their rapid dissemination across different bacterial species through horizontal gene transfer (Wikipedia, 2024). This genetic mobility is a primary driver of the global antimicrobial resistance crisis, rendering standard-of-care treatments ineffective for common infections (WHO, 2023). While traditional drugs target the protein products of these genes, emerging biotech strategies utilize CRISPR-Cas9, antisense oligonucleotides, and peptide nucleic acids to target the ARGs themselves. By silencing or deleting these sequences, these therapies aim to restore the efficacy of existing antibiotics or selectively eliminate multi-drug resistant pathogens from a population (Science Translational Medicine, 2017).

Other names
Antimicrobial resistance geneDrug resistance geneResistome (collective)R-plasmid genes
02

Mechanism of action

Gene silencing or site-specific genomic cleavage to eliminate the genetic determinants of resistance, thereby restoring antibiotic susceptibility or selectively killing resistant bacteria (Nature Biotechnology, 2014; Cell, 2020).

03

Biological functions

Enzymatic inactivationEfflux pump regulationTarget modificationHorizontal gene transferMetabolic bypass
04

Disease associations

InfectionSepsisMultidrug-resistant infectionPneumoniaUrinary tract infection
05

Safety considerations

Off-target effects on host genomic DNADisruption of the beneficial commensal microbiomeHorizontal gene transfer of modified genetic elementsRapid evolution of compensatory resistance mutationsDelivery vehicle immunogenicity (e.g., phage or nanoparticle vectors)
06

Interacting drugs

Antisense oligonucleotides

3 more in the full profile.

07

Biomarkers

mecA (Methicillin resistance)vanA/vanB (Vancomycin resistance)blaKPC (Carbapenem resistance)blaNDM-1 (New Delhi metallo-beta-lactamase)mcr-1 (Colistin resistance)

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