Site-directed mutagenesis of Mycobacterium tuberculosis and functional validation to investigate potential bedaquiline resistance-causing mutations

• Published in: Scientific reports 2023-06, Vol.13 (1), p.9212-9212, Article 9212
• Main Authors: Otum, Christian C., Rivière, Emmanuel, Barnard, Monique, Loubser, Johannes, Williams, Monique J., Streicher, Elizabeth M., Van Rie, Annelies, Warren, Robin M., Klopper, Marisa
• Format: Article
• Language: English
• Subjects: 631/114; 631/1647; 631/326; 631/337; 692/699; 692/699/255; 692/699/255/1856; ATP synthase; Complementation; Genomes; Genotypes; Homologous recombination; Humanities and Social Sciences; Minimum inhibitory concentration; multidisciplinary; Mutation; Mycobacterium tuberculosis; Science; Science (multidisciplinary); Site-directed mutagenesis; Strains (organisms); Tuberculosis; Whole genome sequencing
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-023-35563-0

Molecular detection of bedaquiline resistant tuberculosis is challenging as only a small proportion of mutations in candidate bedaquiline resistance genes have been statistically associated with phenotypic resistance. We introduced two mutations, atpE Ile66Val and Rv0678 Thr33Ala, in the Mycobacterium tuberculosis H37Rv reference strain using homologous recombineering or recombination to investigate the phenotypic effect of these mutations. The genotype of the resulting strains was confirmed by Sanger- and whole genome sequencing, and bedaquiline susceptibility was assessed by minimal inhibitory concentration (MIC) assays. The impact of the mutations on protein stability and interactions was predicted using mutation Cutoff Scanning Matrix (mCSM) tools. The atpE Ile66Val mutation did not elevate the MIC above the critical concentration (MIC 0.25–0.5 µg/ml), while the MIC of the Rv0678 Thr33Ala mutant strains (> 1.0 µg/ml) classifies the strain as resistant, confirming clinical findings. In silico analyses confirmed that the atpE Ile66Val mutation minimally disrupts the bedaquiline-ATP synthase interaction, while the Rv0678 Thr33Ala mutation substantially affects the DNA binding affinity of the MmpR transcriptional repressor. Based on a combination of wet-lab and computational methods, our results suggest that the Rv0678 Thr33Ala mutation confers resistance to BDQ, while the atpE Ile66Val mutation does not, but definite proof can only be provided by complementation studies given the presence of secondary mutations.