Faculty of Life Sciences, Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.
National Institute for Infectious Diseases "L. Spallanzani"-IRCCS, Rome, Italy.
PLoS One. 2020 Oct 12;15(10):e0240250. doi: 10.1371/journal.pone.0240250. eCollection 2020.
The impact of tuberculosis and of anti-tuberculosis therapy on composition and modification of human lung microbiota has been the object of several investigations. However, no clear outcome has been presented so far and the relationship between M. tuberculosis pulmonary infection and the resident lung microbiota remains vague. In this work we describe the results obtained from a multicenter study of the microbiota of sputum samples from patients with tuberculosis or unrelated lung diseases and healthy donors recruited in Switzerland, Italy and Bangladesh, with the ultimate goal of discovering a microbiota-based biomarker associated with tuberculosis. Bacterial 16S rDNA amplification, high-throughput sequencing and extensive bioinformatic analyses revealed patient-specific flora and high variability in taxon abundance. No common signature could be identified among the individuals enrolled except for minor differences which were not consistent among the different geographical settings. Moreover, anti-tuberculosis therapy did not cause any important variation in microbiota diversity, thus precluding its exploitation as a biomarker for the follow up of tuberculosis patients undergoing treatment.
结核病和抗结核治疗对人肺微生物组的组成和修饰的影响已经成为了几个研究的对象。然而,到目前为止,还没有提出明确的结果,结核分枝杆菌肺部感染与常驻肺微生物组之间的关系仍然不清楚。在这项工作中,我们描述了一项来自瑞士、意大利和孟加拉国的结核病或非相关肺部疾病患者和健康供体的痰样本的多中心研究中获得的结果,其最终目标是发现与结核病相关的基于微生物组的生物标志物。细菌 16S rDNA 扩增、高通量测序和广泛的生物信息学分析揭示了患者特有的菌群和分类群丰度的高度可变性。除了在不同地理环境中不一致的微小差异外,无法在入组个体中确定共同的特征。此外,抗结核治疗并没有导致微生物组多样性的任何重要变化,因此排除了将其作为治疗中结核病患者随访的生物标志物的可能性。