Li Jingjing, Yang Zhongli, Yuan Wenji, Bao Zhiwei, Li Ming D
State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Institute of Biomedical Big Data, School of Ophthalmology and Optometry and Eye Hospital, School of Biomedical Engineering, Wenzhou Medical University, Wenzhou, China.
Nicotine Tob Res. 2024 May 22;26(6):742-751. doi: 10.1093/ntr/ntad209.
The number of smokers worldwide increased greatly during the past decades and reached 1.14 billion in 2019, becoming a leading risk factor for human health. Tobacco smoking has wide effects on human genetics, epigenetics, transcriptome, and gut microbiome. Although many studies have revealed effects of smoking on host transcriptome, research on the relationship between smoking, host gene expression, and the gut microbiome is limited.
We first explored transcriptome and metagenome profile differences between smokers and nonsmokers. To evaluate the relationship between host gene expression and gut microbiome, we then applied bidirectional mediation analysis to infer causal relationships between smoking, gene expression, and gut microbes.
Metagenome and transcriptome analyses revealed 71 differential species and 324 differential expressed genes between smokers and nonsmokers. With smoking as an exposure variable, we identified 272 significant causal relationships between gene expression and gut microbes, among which there were 247 genes that mediate the effect of smoking on gut microbes. Pathway-based enrichment analysis showed that these genes were significantly enriched in heme metabolic pathway, which mainly mediated the changes of Bacteroides finegoldii and Lachnospiraceae bacterium 9_1_43BFAA. Additionally, by performing metabolome data analysis in the Integrated Human Microbiome Project (iHMP) database, we verified the correlation between the intermediate products of the heme metabolism pathway (porphobilinogen, bilirubin, and biliverdin) and gut microbiome.
By investigating the bidirectional interaction between smoking-related host gene expression and gut microbes, this study provided evidence for the mediation of smoking on gut microbes through co-involvement or interaction of heme metabolism.
By comparing the metagenome and transcriptome sequencing profiles between 34 smokers and 33 age- and gender-matched nonsmokers, we are the first to reveal causal relationships among tobacco smoking, host gene expression, and gut microbes. These findings offer insight into how smoking affects gut microbes through host gene expression and metabolism, which highlights the importance of heme metabolism in modulating the effects of smoking on gut microbiome.
在过去几十年中,全球吸烟者数量大幅增加,2019年达到11.4亿,成为人类健康的主要风险因素。吸烟对人类遗传学、表观遗传学、转录组和肠道微生物群有广泛影响。尽管许多研究揭示了吸烟对宿主转录组的影响,但关于吸烟、宿主基因表达和肠道微生物群之间关系的研究仍然有限。
我们首先探究吸烟者和非吸烟者之间的转录组和宏基因组特征差异。为了评估宿主基因表达与肠道微生物群之间的关系,我们随后应用双向中介分析来推断吸烟、基因表达和肠道微生物之间的因果关系。
宏基因组和转录组分析揭示了吸烟者和非吸烟者之间71种差异物种和324个差异表达基因。以吸烟作为暴露变量,我们确定了基因表达与肠道微生物之间272个显著的因果关系,其中有247个基因介导吸烟对肠道微生物的影响。基于通路的富集分析表明,这些基因在血红素代谢通路中显著富集,该通路主要介导了纤细拟杆菌和9_1_43BFAA科梭菌的变化。此外,通过在综合人类微生物组计划(iHMP)数据库中进行代谢组数据分析,我们验证了血红素代谢通路中间产物(胆色素原、胆红素和胆绿素)与肠道微生物群之间的相关性。
通过研究吸烟相关的宿主基因表达与肠道微生物之间的双向相互作用,本研究为吸烟通过血红素代谢的共同参与或相互作用对肠道微生物的介导作用提供了证据。
通过比较34名吸烟者和33名年龄及性别匹配的非吸烟者之间的宏基因组和转录组测序图谱,我们首次揭示了吸烟、宿主基因表达和肠道微生物之间的因果关系。这些发现为吸烟如何通过宿主基因表达和代谢影响肠道微生物提供了见解,突出了血红素代谢在调节吸烟对肠道微生物群影响方面的重要性。