The impact of genotype on the phenotype of Mycobacterium tuberculosis ΔsufR mutants

• Published in: Tuberculosis (Edinburgh, Scotland) Scotland), 2023-07, Vol.141, p.102360-102360, Article 102360
• Main Authors: Willemse, Danicke, Baatjies, Lucinda, Dippenaar, Anzaan, Warren, Robin M., Williams, Monique J.
• Format: Article
• Language: English
• Subjects: Bacterial Proteins - genetics; Bacterial Proteins - metabolism; Genotype; Iron-Sulfur Proteins - genetics; Iron-sulphur cluster; Mycobacterium tuberculosis; Phenotype; Regulation; rv1460; SufR
• ISSN: 1472-9792; 1873-281X
• DOI: 10.1016/j.tube.2023.102360

Iron-sulphur (FeS) cluster biogenesis is a tightly regulated process in vivo. In Mycobacterium tuberculosis (Mtb), SufR functions as a transcriptional repressor of the operon encoding the primary FeS cluster biogenesis system. Previously, three independently isolated mutants (ΔRv1460stop_1.19, ΔRv1460stop _5.19 and ΔRv1460stop _5.20) harbouring the same deletion in sufR, displayed different growth kinetics in OADC supplemented 7H9 media. To investigate this discrepancy, we performed whole genome sequencing of the 3 mutants and the wild-type progenitor. Single nucleotide polymorphisms (SNPs) were identified in 3 genes in the ΔRv1460stop_1.19 mutant and one gene in the ΔRv1460stop_5.20 mutant. Phenotyping of the ΔRv1460stop_5.19 mutant, which had no additional SNPs, revealed increased susceptibility to clofazimine, DMNQ and menadione, while uptake and survival in THP-1 cells were not significantly different from the wild-type strain. Given that these results differ from those reported for other sufR deletion mutants (ΔSufRMTB and MtbΔSufR), they suggest that the position of the sufR deletion and the genotype of the progenitor strain impact the resulting phenotype.