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从痰标本中 DNA 清除情况的纵向分析看,是否真的需要一种新的治疗模式来发现可培养的差异结核分枝杆菌?

Does discovery of differentially culturable M tuberculosis really demand a new treatment paradigm? Longitudinal analysis of DNA clearance from sputum.

机构信息

Pulmonary Section, Denver VA Medical Center, Denver, CO, USA.

Division of Pulmonary Sciences and Critical Care Medicine, University of Colorado Denver, Aurora, CO, USA.

出版信息

BMC Infect Dis. 2018 Jul 3;18(1):293. doi: 10.1186/s12879-018-3213-7.

Abstract

BACKGROUND

According to the traditional tuberculosis (TB) treatment paradigm, the initial doses of treatment rapidly kill most Mycobacterium tuberculosis (Mtb) bacilli in sputum, yet many more months of daily treatment are required to eliminate a small, residual subpopulation of drug-tolerant bacilli. This paradigm has recently been challenged following the discovery that up to 90% of Mtb bacilli in sputum are culturable only with growth-factor supplementation. These "differentially culturable" bacilli are hypothesized to be more drug-tolerant than routinely culturable bacilli. This hypothesis implies an alternative paradigm in which TB treatment does not rapidly reduce the total Mtb population but only the small, routinely culturable subpopulation. To evaluate these competing paradigms, we developed a culture-independent method for quantifying the viable fraction of Mtb bacilli in sputum during treatment.

METHODS

We used GeneXpert MTB/RIF to quantify Mtb DNA in sputa collected longitudinally from Ugandan adults taking standard 4-drug treatment for drug-susceptible pulmonary TB. We modeled GeneXpert cycle thresholds over time using nonlinear mixed-effects regression. We adjusted these models for clearance of DNA from killed-but-not-yet-degraded bacilli, assuming clearance half-lives ranging from 0 to 1.25 days. We used a convolution integral to quantify DNA from viable bacilli only, and converted cycle thresholds to Mtb genomic equivalents. We replicated our results in a South African cohort.

RESULTS

We enrolled 41 TB patients in Uganda. Assuming a DNA-clearance half-life of 0 days, genomic equivalents of viable sputum bacilli decreased by 0.22 log/day until 8.8 days, then by 0.07 log/day afterwards. Assuming a DNA-clearance half-life of 1.25 days, genomic equivalents of viable bacilli decreased by 0.36 log/day until 5.0 days, then by 0.06 log/day afterwards. By day 7, viable Mtb had decreased by 97.2-98.8%. We found similar results for 19 TB patients in South Africa.

DISCUSSION

Using a culture-independent method, we found that TB treatment rapidly eliminates most viable Mtb in sputum. These findings are incompatible with the hypothesis that differentially culturable bacilli are drug-tolerant.

CONCLUSIONS

A culture-independent method for measuring viable Mtb in sputum during treatment corroborates the traditional TB treatment paradigm in which a rapid bactericidal phase precedes slow, elimination of a small, residual bacillary subpopulation.

摘要

背景

根据传统的结核病(TB)治疗模式,治疗的初始剂量会迅速杀死痰液中大多数结核分枝杆菌(Mtb)杆菌,但仍需要数月的每日治疗才能消除一小部分耐药杆菌的残余亚群。这一模式在发现痰液中多达 90%的 Mtb 杆菌仅在添加生长因子时才能培养后受到了挑战。这些“差异可培养”的杆菌被假设比常规可培养的杆菌更具耐药性。这一假设意味着,在替代的 TB 治疗模式中,治疗不会迅速降低总 Mtb 种群,而只是降低小的、常规可培养的亚群。为了评估这两种相互竞争的模式,我们开发了一种在治疗过程中定量检测痰液中 Mtb 杆菌存活分数的无培养方法。

方法

我们使用 GeneXpert MTB/RIF 定量检测来自接受标准 4 种药物治疗的耐药性肺结核的乌干达成年人的痰液中 Mtb DNA。我们使用非线性混合效应回归模型来模拟 GeneXpert 循环阈值随时间的变化。我们对这些模型进行了调整,以清除从已杀死但尚未降解的杆菌中清除 DNA,假设清除半衰期范围为 0 至 1.25 天。我们使用卷积积分仅定量活杆菌的 DNA,并将循环阈值转换为 Mtb 基因组当量。我们在南非队列中复制了我们的结果。

结果

我们在乌干达招募了 41 名结核病患者。假设 DNA 清除半衰期为 0 天,活痰杆菌的基因组当量在 8.8 天前每天减少 0.22 对数,之后每天减少 0.07 对数。假设 DNA 清除半衰期为 1.25 天,活杆菌的基因组当量在 5.0 天前每天减少 0.36 对数,之后每天减少 0.06 对数。到第 7 天,活 Mtb 减少了 97.2-98.8%。我们在南非的 19 名结核病患者中也发现了类似的结果。

讨论

使用无培养方法,我们发现治疗迅速消除了痰液中大多数活 Mtb。这些发现与差异可培养杆菌具有耐药性的假设不符。

结论

一种用于测量治疗过程中痰液中活 Mtb 的无培养方法证实了传统的 TB 治疗模式,即快速杀菌阶段之后是缓慢消除一小部分残留的杆菌亚群。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6920/6029172/c63e2a178b00/12879_2018_3213_Fig1_HTML.jpg

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