SNPs in genes related to the repair of damage to DNA in clinical isolates of M. tuberculosis: A transversal and longitudinal approach.
Damián Eduardo Pérez-MartínezRoberto Zenteno-CuevasPublished in: PloS one (2024)
The presence of SNPs in genes related to DNA damage repair in M. tuberculosis can trigger hypermutagenic phenotypes with a higher probability of generating drug resistance. The aim of this research was to compare the presence of SNPs in genes related to DNA damage repair between sensitive and DR isolates, as well as to describe the dynamics in the presence of SNPs in M. tuberculosis isolated from recently diagnosed TB patients of the state of Veracruz, Mexico. The presence of SNPs in the coding regions of 65 genes related to DNA damage repair was analyzed. Eighty-six isolates from 67 patients from central Veracruz state, Mexico, were sequenced. The results showed several SNPs in 14 genes that were only present in drug-resistant genomes. In addition, by following of 15 patients, it was possible to describe three different dynamics of appearance and evolution of non-synonymous SNPs in genes related to DNA damage repair: 1) constant fixed SNPs, 2) population substitution, and 3) gain of fixed SNPs. Further research is required to discern the biological significance of each of these pathways and their utility as markers of DR or for treatment prognosis.
Keyphrases
- genome wide
- dna damage
- drug resistant
- end stage renal disease
- oxidative stress
- newly diagnosed
- mycobacterium tuberculosis
- ejection fraction
- dna repair
- peritoneal dialysis
- emergency department
- bioinformatics analysis
- gene expression
- hiv aids
- cross sectional
- pseudomonas aeruginosa
- hepatitis c virus
- cystic fibrosis
- smoking cessation
- acinetobacter baumannii
- patient reported
- genetic diversity