Section of Infectious Diseases, Boston University School of Medicine, Boston, Massachusetts, USA.
Center for Communicable Disease Dynamics, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.
Clin Infect Dis. 2024 Feb 17;78(2):269-276. doi: 10.1093/cid/ciad596.
Emerging resistance to bedaquiline (BDQ) threatens to undermine advances in the treatment of drug-resistant tuberculosis (DRTB). Characterizing serial Mycobacterium tuberculosis (Mtb) isolates collected during BDQ-based treatment can provide insights into the etiologies of BDQ resistance in this important group of DRTB patients.
We measured mycobacteria growth indicator tube (MGIT)-based BDQ minimum inhibitory concentrations (MICs) of Mtb isolates collected from 195 individuals with no prior BDQ exposure who were receiving BDQ-based treatment for DRTB. We conducted whole-genome sequencing on serial Mtb isolates from all participants who had any isolate with a BDQ MIC >1 collected before or after starting treatment (95 total Mtb isolates from 24 participants).
Sixteen of 24 participants had BDQ-resistant TB (MGIT MIC ≥4 µg/mL) and 8 had BDQ-intermediate infections (MGIT MIC = 2 µg/mL). Participants with pre-existing resistance outnumbered those with resistance acquired during treatment, and 8 of 24 participants had polyclonal infections. BDQ resistance was observed across multiple Mtb strain types and involved a diverse catalog of mmpR5 (Rv0678) mutations, but no mutations in atpE or pepQ. Nine pairs of participants shared genetically similar isolates separated by <5 single nucleotide polymorphisms, concerning for potential transmitted BDQ resistance.
BDQ-resistant TB can arise via multiple, overlapping processes, including transmission of strains with pre-existing resistance. Capturing the within-host diversity of these infections could potentially improve clinical diagnosis, population-level surveillance, and molecular diagnostic test development.
贝达喹啉(BDQ)耐药性的出现威胁到耐药结核病(DRTB)治疗方面的进展。对基于 BDQ 治疗期间收集的连续结核分枝杆菌(Mtb)分离株进行特征分析,可以深入了解这组重要的 DRTB 患者中 BDQ 耐药的病因。
我们测量了 195 名无 BDQ 既往暴露的 DRTB 患者在接受基于 BDQ 的治疗期间收集的结核分枝杆菌生长指示管(MGIT)基于 BDQ 的最小抑菌浓度(MIC)。我们对所有在治疗前或治疗后任何分离株的 BDQ MIC>1 的参与者的连续 Mtb 分离株进行全基因组测序(共来自 24 名参与者的 95 个 Mtb 分离株)。
24 名参与者中有 16 名患有 BDQ 耐药性结核病(MGIT MIC≥4μg/mL),8 名患有 BDQ 中介感染(MGIT MIC=2μg/mL)。有预先存在耐药性的参与者多于在治疗过程中获得耐药性的参与者,24 名参与者中有 8 名患有多克隆感染。BDQ 耐药性发生在多个 Mtb 菌株类型中,涉及到多种 mmpR5(Rv0678)突变,但没有 atpE 或 pepQ 突变。9 对参与者共享了遗传上相似的分离株,它们之间的差异<5 个单核苷酸多态性,令人担忧潜在的传播性 BDQ 耐药性。
BDQ 耐药性结核病可以通过多种重叠的过程出现,包括传播预先存在耐药性的菌株。捕获这些感染的宿主内多样性可能有助于改善临床诊断、人群监测和分子诊断测试的开发。