Infectious Disease Research Collaboration, Kampala, Uganda.
Department of Biochemistry, Makerere University, Kampala, Uganda.
Microbiol Spectr. 2021 Oct 31;9(2):e0048121. doi: 10.1128/Spectrum.00481-21. Epub 2021 Sep 8.
There is a critical need for improved pharmacodynamic markers for use in human tuberculosis (TB) drug trials. Pharmacodynamic monitoring in TB has conventionally used culture or molecular methods to enumerate the burden of Mycobacterium tuberculosis organisms in sputum. A recently proposed assay called the rRNA synthesis (RS) ratio measures a fundamentally novel property, how drugs impact ongoing bacterial rRNA synthesis. Here, we evaluated RS ratio as a potential pharmacodynamic monitoring tool by testing pretreatment sputa from 38 Ugandan adults with drug-susceptible pulmonary TB. We quantified the RS ratio in paired pretreatment sputa and evaluated the relationship between the RS ratio and microbiologic and molecular markers of M. tuberculosis burden. We found that the RS ratio was highly repeatable and reproducible in sputum samples. The RS ratio was independent of M. tuberculosis burden, confirming that it measures a distinct new property. In contrast, markers of M. tuberculosis burden were strongly associated with each other. These results indicate that the RS ratio is repeatable and reproducible and provides a distinct type of information from markers of M. tuberculosis burden. This study takes a major next step toward practical application of a novel pharmacodynamic marker that we believe will have transformative implications for tuberculosis. This article follows our recent report in that an assay called the rRNA synthesis (RS) ratio indicates the treatment-shortening of drugs and regimens. Distinct from traditional measures of bacterial burden, the RS ratio measures a fundamentally novel property, how drugs impact ongoing bacterial rRNA synthesis.
迫切需要改进用于人类结核病 (TB) 药物试验的药效动力学标志物。TB 的药效动力学监测传统上使用培养或分子方法来计算痰中结核分枝杆菌的负担。最近提出的一种称为 rRNA 合成 (RS) 比的测定方法测量了一个全新的特性,即药物如何影响正在进行的细菌 rRNA 合成。在这里,我们通过测试来自 38 名乌干达药物敏感型肺结核成年人的预处理痰液来评估 RS 比作为潜在的药效动力学监测工具。我们在配对的预处理痰液中定量了 RS 比,并评估了 RS 比与结核分枝杆菌负担的微生物学和分子标志物之间的关系。我们发现 RS 比在痰液样本中具有高度可重复性和重现性。RS 比与结核分枝杆菌负担无关,这证实了它测量了一个全新的特性。相比之下,结核分枝杆菌负担的标志物彼此之间存在强烈的相关性。这些结果表明,RS 比具有可重复性和重现性,并提供了与结核分枝杆菌负担标志物不同的信息类型。本研究朝着实用新型药效动力学标志物迈出了重要的下一步,我们相信这将对结核病产生变革性的影响。这篇文章延续了我们最近在 中的报告,该报告表明一种称为 rRNA 合成 (RS) 比的测定方法可以指示药物和方案的缩短治疗时间。与传统的细菌负担测量方法不同,RS 比测量了一个全新的特性,即药物如何影响正在进行的细菌 rRNA 合成。