Browse AMR Genes
Explore antimicrobial resistance genes from the literature
Explore antimicrobial resistance genes from the literature
glycosyltransferase
Overview
| Loss of function |
| Mycobacterium tuberculosis |
Ethionamide |
Reslit |
| Candidate |
| G356D | - | Loss of function | Mycobacterium tuberculosis | Ethionamide | Reslit | Candidate |
| R273C | - | Loss of function | Mycobacterium tuberculosis | Ethionamide | Reslit | Candidate |
| A422V | - | - | - | Ethionamide | Reslit | Candidate |
| V237L | - | - | - | Ethionamide | Reslit | Candidate |
| H178R | - | - | Mycobacterium tuberculosis | Ethionamide | Reslit | Candidate |
| Y155S | - | - | Mycobacterium tuberculosis | Ethionamide | Reslit | Candidate |
| V171G | - | - | Mycobacterium tuberculosis | Ethionamide | Reslit | Candidate |
| A35V | - | - | Mycobacterium tuberculosis | Isoniazid | Reslit | Candidate |
| F355S | - | single resistance variant | Mycobacterium tuberculosis | ProthionamideIsoniazid | Card Database | Established |
| - | Loss of function | Mycobacterium tuberculosis | Ethionamide | Reslit | Candidate |
Mycothiol biosynthesis is essential for ethionamide susceptibility in Mycobacterium tuberculosis.
Mutations in the mshA gene, which is involved in mycothiol biosynthesis, confer co-resistance to isoniazid and ethionamide in Mycobacterium tuberculosis.
Resistance to Isoniazid and Ethionamide in Mycobacterium tuberculosis: Genes, Mutations, and Causalities.
The study identifies key genes and mutations involved in resistance to isoniazid (INH) and ethionamide (ETH) in Mycobacterium tuberculosis, highlighting the role of katG, inhA, and ethA in resistance mechanisms.
Efficacy of β-lactam/β-lactamase inhibitor combination is linked to WhiB4-mediated changes in redox physiology of Mycobacterium tuberculosis.
The study identifies BlaC as a β-lactamase in Mycobacterium tuberculosis that contributes to β-lactam resistance, and shows that WhiB4 modulates its expression in a redox-dependent manner.
Investigating resistance in clinical Mycobacterium tuberculosis complex isolates with genomic and phenotypic antimicrobial susceptibility testing: a multicentre observational study.
The study identifies various AMR genes and mutations in Mycobacterium tuberculosis complex isolates, including rpoB, fabG1, inhA, ndh, katG, mshA, ahpC, gyrA, gyrB, rrs, eis, embCAB, pncA, and rpsA, which are associated with resistance to rifampicin, isoniazid, fluoroquinolones, aminoglycosides, ethambutol, and pyrazinamide.
The MAGMA pipeline for comprehensive genomic analyses of clinical Mycobacterium tuberculosis samples.
The MAGMA pipeline was developed for comprehensive genomic analyses of clinical Mycobacterium tuberculosis samples, demonstrating improved detection of drug resistance variants compared to existing pipelines like MTBseq. It successfully identified various AMR genes and mutations associated with resistance to multiple anti-TB drugs.
Leveraging large-scale Mycobacterium tuberculosis whole genome sequence data to characterise drug-resistant mutations using machine learning and statistical approaches.
The study identifies several genes and mutations associated with drug resistance in Mycobacterium tuberculosis, including pncA, ethA, ndh, mshA, embR, rpoB, inhA, gyrA, and Rv0678, along with their respective mutations that confer resistance to pyrazinamide, ethionamide, isoniazid, rifampicin, ethambutol, fluoroquinolones, bedaquiline, and clofazimine.
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