Abstract
ABSTRACTThere 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.IMPORTANCE 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 Nature Communications 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.
Highlights
IMPORTANCE This study takes a major step toward practical application of a novel pharmacodynamic marker that we believe will have transformative implications for tuberculosis
In the paired pretreatment sputa, the rRNA synthesis (RS) ratio was quantifiable in 97% of first sputum samples (SS1) and 92% of second sputum samples (SS2)
We found that the RS ratio was highly repeatable in technical replicates and had high interobserver reproducibility
Summary
IMPORTANCE This study takes a major step toward practical application of a novel pharmacodynamic marker that we believe will have transformative implications for tuberculosis. Key insights from in vitro and murine studies are (i) drugs often affect the RS ratio and CFU burden differently and (ii) the RS ratio appears to indicate the sterilizing activity of drugs and regimens [9]. This novel molecular approach has yet to be extensively investigated as a marker in humans. We tested the repeatability and reproducibility of the RS ratio in paired pretreatment sputa and evaluated the association of the RS ratio with conventional and investigational PD markers that enumerate M. tuberculosis burden. Our results suggest that the RS ratio is repeatable and reproducible and provide a distinct new type of information
Published Version (Free)
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have