State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Centre for Infectious Diseases, Collaborative Innovation Centre for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital,Zhejiang University School of Medicine, Hangzhou, 310003, China.
Microb Biotechnol. 2022 Jan;15(1):262-275. doi: 10.1111/1751-7915.13761. Epub 2021 Feb 18.
Intestinal flora provides an important contribution to the development of pulmonary tuberculosis (PTB). We performed a cross-sectional study in 52 healthy controls (HCs) and 83 patients with untreated active PTB to assess the differences in their microbiomic and metabolic profiles in faeces via V3-V4 16S rRNA gene sequencing and gas chromatography-mass spectrometry. Patients with PTB had considerable reductions in phylogenetic alpha diversity and the production of short-chain fatty acids, dysbiosis of the intestinal flora and alterations in the faecal metabolomics composition compared with HCs. Significant alterations in faecal metabolites were associated with changes in the relative abundance of specific genera. Our study describes the imbalance of the gut microbiota and altered faecal metabolomics profiles in patients with PTB; the results indicate that the gut microbiota and faecal metabolomic profiles can be used as potential preventive and therapeutic targets for PTB.
肠道菌群对肺结核(PTB)的发展有重要贡献。我们对 52 名健康对照(HC)和 83 名未经治疗的活动性肺结核患者进行了一项横断面研究,通过 V3-V4 16S rRNA 基因测序和气相色谱-质谱联用技术评估粪便中微生物组和代谢组谱的差异。与 HCs 相比,PTB 患者的系统发育 alpha 多样性和短链脂肪酸的产生、肠道菌群失调以及粪便代谢组组成的改变都有明显的减少。粪便代谢物的显著变化与特定属的相对丰度的变化有关。本研究描述了肺结核患者肠道微生物群失衡和粪便代谢组学特征的改变;结果表明,肠道微生物群和粪便代谢组学特征可作为肺结核的潜在预防和治疗靶点。