Department of Biotechnology, Institute of Natural and Applied Sciences, Çukurova University, 01330, Balcalı, Adana, Türkiye.
Biology Department, Faculty of Education and Arts, Sohar University, Sohar, 311, Sultanate of Oman.
Curr Mol Pharmacol. 2024;17:e18761429314641. doi: 10.2174/0118761429314641240815080447.
Reduced bedaquiline (BDQ) sensitivity to antimycobacterial drugs has been linked to mutations in the Rv0678, pepQ, and Rv1979c genes of Mycobacterium tuberculosis (MTB). Resistance-causing mutations in MTB strains under treatment may have an impact on novel BDQ-based medication regimens intended to reduce treatment time. Due to this, we investigated the genetic basis of BDQ resistance in Turkish TB patients with MTB clinical isolates. Furthermore, mutations in the genes linked to efflux pumps were examined as a backup resistance mechanism.
We scrutinized 100 MTB clinical isolates from TB patients using convenience sampling. Eighty MDR and twenty pan-drug susceptible MTB strains were among these isolates. Sequencing was performed on all strains, and genomic analyses were performed to find mutations in BDQ resistance-associated genes, including Rv0678 and pepQ(Rv2535c), which correspond to a putative Xaa-Pro aminopeptidase, and Rv1979c. Of the 74 isolates with PepQ (Rv2535c) mutations, four isolates (2.96%) exhibited MGIT-BDQ susceptibility.
Twenty-one (19.11%) of the ninety-one isolates carrying mutations, including Rv1979c, were MGIT-BDQ-sensitive. Nonetheless, out of the 39 isolates with Rv0678 mutations, four (2.96%) were sensitive to MGIT-BDQ. It was found that resistance-associated variants (RAVs) in Rv0678, pepQ, and Rv1979c are often linked to BDQ resistance.
In order to include variations in efflux pump genes in genome-based diagnostics for drug-resistant MTB, further evidence about their involvement in resistance is needed.
结核分枝杆菌(MTB)中 Rv0678、pepQ 和 Rv1979c 基因的突变与 bedaquiline(BDQ)对抗结核药物的敏感性降低有关。治疗中耐药 MTB 菌株的耐药突变可能会影响旨在缩短治疗时间的新型 BDQ 为基础的药物治疗方案。因此,我们研究了土耳其结核患者 MTB 临床分离株中 BDQ 耐药的遗传基础。此外,还检查了与外排泵相关的基因中的突变作为备用耐药机制。
我们使用便利抽样法检查了 100 株来自结核患者的 MTB 临床分离株。这些分离株中包括 80 株 MDR 和 20 株泛耐药 MTB 株。对所有菌株进行测序,并进行基因组分析,以寻找与 BDQ 耐药相关的基因(包括 Rv0678 和 pepQ[Rv2535c])中的突变,该基因对应于一个假定的 Xaa-Pro 氨肽酶,以及 Rv1979c。在携带 PepQ(Rv2535c)突变的 74 株分离株中,有 4 株(2.96%)对 MGIT-BDQ 具有敏感性。
携带包括 Rv1979c 在内的突变的 91 株分离株中的 21 株(19.11%)对 MGIT-BDQ 敏感。然而,在 39 株 Rv0678 突变的分离株中,有 4 株(2.96%)对 MGIT-BDQ 敏感。发现 Rv0678、pepQ 和 Rv1979c 中的耐药相关变异(RAVs)通常与 BDQ 耐药相关。
为了将外排泵基因的变异纳入基于基因组的耐药 MTB 诊断,需要进一步证明它们与耐药性有关。