全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

烟草暴露与人类肠道菌群相关性探究
Exploring the Correlation between Tobacco Exposure and Human Intestinal Flora

DOI: 10.12677/AMB.2023.122009, PP. 71-82

Keywords: 烟草暴露,肠道菌群,16S rDNA,Blautia菌属,Roseburia菌属
Tobacco Exposure
, Intestinal Flora, 16S rDNA, Blautia, Roseburia

Full-Text   Cite this paper   Add to My Lib

Abstract:

目的:探究不同烟草暴露程度健康人群的肠道菌群是否存在差异,挖掘烟草暴露对肠道菌群的影响。方法:收集符合纳入标准的各组人员的粪便样本,其中烟草暴露组(>400年支) (A组) 17例、烟草暴露组(<400年支) (B组) 16例、长期二手烟暴露组(C组) 16例、戒烟组(戒烟6月以上) (D组) 14例及无烟草暴露组(E组) 17例。对上述每份粪便样本进行16S rDNA高通量测序,随后进行OTU分析及物种注释、样本复杂度分析、多样本比较分析及组间群落结构差异显著性分析。结果:A组、B组、D组在菌种组成更为接近,而C组、E组在菌种组成上更为接近。但各组间菌群丰富度、多样性、群落分布无显著异常。在门水平上,部分组间在厚壁菌门(Firmicutes)及变形菌门(Proteobacteria)存在差异(p < 0.05)。在属水平上,Agathobacter属、Blautia属、f_Lachnospiraceae_Unclassified属、Roseburia属、Subdoligranulum属在不同组间存在统计学差异(p < 0.05)。结论:不同程度的烟草暴露人群的肠道菌群多样性未发现明确的差异,但Blautia菌属及Roseburia菌属与烟草暴露程度呈负相关性,值得进一步研究。
Objective: To investigate whether there are differences in the intestinal flora of healthy people with different levels of tobacco exposure, and explore the effects of tobacco exposure on the intestinal flora. Methods: Fecal samples were collected from 80 volunteers, including 17 cases in the tobacco exposure group (Smoking Index > 400) (group A), 16 cases in the tobacco exposure group (Smoking Index < 400) (group B), 16 cases in the long-term second-hand smoke exposure group (group C), 14 cases in the smoking cessation group (more than 6 months) (group D) and 17 cases in the non-tobacco exposure group (group E). Each of the above fecal samples was analyzed by 16SrDNA, and OTU analysis and species annotation, Alpha diversity, Beta diversity, significance analysis of community structure differences were performed between groups. Results: Groups A, B and D were closer in intestinal flora composition, while groups C and E were closer in composition. There were no significant abnormalities in the richness, diversity and community distribution of the intestinal flora between the groups. At the Phylum level,there were significantly differences between the some groups of Firmicutes and Proteobacteria (p < 0.05). At the Genus level, there were significantly differences between the different groups of Agathobacter, Blautia, f_Lachnospi- raceae_Unclassified, Roseburia, and Subdoligranulum (p < 0.05). Conclusions: Despite there were no clear differences were found in the diversity of intestinal flora in people with different levels of tobacco exposure so far, but the genus Blautia and Roseburia were inversely correlated with tobacco exposure, which is worth further exploring.

References

[1]  DeCarlo, P.F., Avery, A.M. and Waring, M.S. (2018) Thirdhand Smoke Uptake to Aerosol Particles in the Indoor Environment. Science Advances, 4, eaap8368.
https://doi.org/10.1126/sciadv.aap8368
[2]  Georgiopoulos, G., Oikonomou, D., Pateras, K., et al. (2021) A Bayesian Meta-Analysis on Early Tobacco Exposure and Vascular Health: From Childhood to Early Adulthood. European Journal of Preventive Cardiology, 28, 1315-1322.
https://doi.org/10.1177/2047487319883557
[3]  Office on Smoking and Health (US) (2006) The Health Consequences of Involuntary Exposure to Tobacco Smoke: A Report of the Surgeon General. Centers for Disease Control and Prevention (US), Atlanta.
[4]  Zhang, K., Tartarone, A., Pérez-Ríos, M., et al. (2022) Smoking Burden, MPOWER, Future Tobacco Control and Real-World Challenges in China: Reflections on the WHO Report on the Global Tobacco Epidemic 2021. Translational Lung Cancer Research, 11, 117-121.
https://doi.org/10.21037/tlcr-22-27
[5]  Lv, L.-J., Li, S.-H., Li, S.-C., et al. (2019) Early-Onset Preeclampsia Is Associated with Gut Microbial Alterations in Antepartum and Postpartum Women. Frontiers in Cellular and Infection Microbiology, 9, Article 224.
https://doi.org/10.3389/fcimb.2019.00224
[6]  Nakashima, K., Kimura, S., Ogawa, Y., et al. (2018) Chitin-Based Barrier Immunity and Its Loss Predated Mucus- Colonization by Indigenous Gut Microbiota. Nature Communications, 9, Article No. 3402.
https://doi.org/10.1038/s41467-018-05884-0
[7]  Lee, S.H., Yun, Y., Kim, S.J., et al. (2018) Association between Cigarette Smoking Status and Composition of Gut Microbiota: Population-Based Cross-Sectional Study. Journal of Clinical Medicine, 7, Article No. 282.
https://doi.org/10.3390/jcm7090282
[8]  Shanahan, E.R., Shah, A., Koloski, N., et al. (2018) Influence of Cigarette Smoking on the Human Duodenal Mucosa-Associated Microbiota. Microbiome, 6, Article No. 150.
https://doi.org/10.1186/s40168-018-0531-3
[9]  Kalyana Chakravarthy, S., Jayasudha, R., Sai Prashanthi, G., et al. (2018) Dysbiosis in the Gut Bacterial Microbiome of Patients with Uveitis, an Inflammatory Disease of the Eye. Indian Journal of Microbiology, 58, 457-469.
https://doi.org/10.1007/s12088-018-0746-9
[10]  Liu, X., Mao, B., Gu, J., et al. (2021) Blautia—A New Functional Genus with Potential Probiotic Properties? Gut Microbes, 13, Article 1875796.
https://doi.org/10.1080/19490976.2021.1875796
[11]  Kim, M., Kim, N. and Han, J. (2014) Metabolism of Kaempferia parviflora Polymethoxyflavones by Human Intestinal bacterium Bautia sp. MRG-PMF1. Journal of Agricultural and Food Chemistry, 62, 12377-12383.
https://doi.org/10.1021/jf504074n
[12]  Burapan, S., Kim, M. and Han, J. (2017) Curcuminoid Demethylation as an Alternative Metabolism by Human Intestinal Microbiota. Journal of Agricultural and Food Chemistry, 65, 3305-3310.
https://doi.org/10.1021/acs.jafc.7b00943
[13]  Liu, M.-Y., Li, M., Wang, X.-L., et al. (2013) Study on Human Intestinal Bacterium Blautia sp. AUH-JLD56 for the Conversion of Arctigenin to (-)-3’-Desmethylarctigenin. Journal of Agricultural and Food Chemistry, 61, 12060- 12065.
https://doi.org/10.1021/jf403924c
[14]  Vaughn, B.P., Kaiser, T., Staley, C., et al. (2019) A Pilot Study of Fecal Bile Acid and Microbiota Profiles in Inflammatory Bowel Disease and Primary Sclerosing Cholangitis. Clinical and Experimental Gastroenterology, 12, 9-19.
https://doi.org/10.2147/CEG.S186097
[15]  Ozato, N., Saito, S., Yamaguchi, T., et al. (2019) Blautia Genus Associated with Visceral Fat Accumulation in Adults 20-76 Years of Age. NPJ Biofilms and Microbiomes, 5, Article No. 28.
https://doi.org/10.1038/s41522-019-0101-x
[16]  Pataky, Z., Genton, L., Spahr, L., et al. (2016) Impact of Hypocaloric Hyperproteic Diet on Gut Microbiota in Overweight or Obese Patients with Nonalcoholic Fatty Liver Disease: A Pilot Study. Digestive Diseases and Sciences, 61, 2721-2731.
https://doi.org/10.1007/s10620-016-4179-1
[17]  Iida, N., Mizukoshi, E., Yamashita, T., et al. (2019) Overuse of Antianaerobic Drug Is Associated with Poor Postchemotherapy Prognosis of Patients with Hepatocellular Carcinoma. International Journal of Cancer, 145, 2701-2711.
https://doi.org/10.1002/ijc.32339
[18]  Kimura, I., Ozawa, K., Inoue, D., et al. (2013) The Gut Microbiota Suppresses Insulin-Mediated Fat Accumulation via the Short-Chain Fatty Acid Receptor GPR43. Nature Communications, 4, Article No. 1829.
https://doi.org/10.1038/ncomms2852
[19]  Zhernakova, D.V., Le, T.H., Kurilshikov, A., et al. (2018) Individual Variations in Cardiovascular-Disease-Related Protein Levels Are Driven by Genetics and Gut Microbiome. Nature Genetics, 50, 1524-1532.
https://doi.org/10.1038/s41588-018-0224-7
[20]  Grases-Pintó, B., Abril-Gil, M., Castell, M., et al. (2019) Influence of Leptin and Adiponectin Supplementation on Intraepithelial Lymphocyte and Microbiota Composition in Suckling Rats. Frontiers in Immunology, 10, Article 2369.
https://doi.org/10.3389/fimmu.2019.02369
[21]  Liu, F., Li, J., Guan, Y., et al. (2019) Dysbiosis of the Gut Microbiome Is Associated with Tumor Biomarkers in Lung Cancer. International Journal of Biological Sciences, 15, 2381-2392.
https://doi.org/10.7150/ijbs.35980
[22]  Chauhan, N.S., Pandey, R., Mondal, A.K., et al. (2018) Western Indian Rural Gut Microbial Diversity in Extreme Prakriti Endo-Phenotypes Reveals Signature Microbes. Frontiers in Microbiology, 9, Article 118.
https://doi.org/10.3389/fmicb.2018.00118
[23]  Nishino, K., Nishida, A., Inoue, R., et al. (2018) Analysis of Endoscopic Brush Samples Identified Mucosa-Associated Dysbiosis in Inflammatory Bowel Disease. Journal of Gastroenterology, 53, 95-106.
https://doi.org/10.1007/s00535-017-1384-4
[24]  Wang, J., Zhang, C., Guo, C. and Li, X. (2019) Chitosan Ameliorates DSS-Induced Ulcerative Colitis Mice by Enhancing Intestinal Barrier Function and Improving Microflora. International Journal of Molecular Sciences, 20, Article No. 5751.
https://doi.org/10.3390/ijms20225751
[25]  Jost, T., Lacroix, C., Braegger, C.P., Rochat, F. and Chassard, C. (2014) Vertical Mother-Neonate Transfer of Maternal Gut Bacteria via Breastfeeding. Environmental Microbiology, 16, 2891-2904.
https://doi.org/10.1111/1462-2920.12238
[26]  Liu, T., Liang, X., Lei, C., et al. (2020) High-Fat Diet Affects Heavy Metal Accumulation and Toxicity to Mice Liver and Kidney Probably via Gut Microbiota. Frontiers in Microbiology, 11, Article 1604.
https://doi.org/10.3389/fmicb.2020.01604
[27]  Lachmandas, E., van den Heuvel, C.N., Damen, M.S., et al. (2016) Diabetes Mellitus and Increased Tuberculosis Susceptibility: The Role of Short-Chain Fatty Acids. Journal of Diabetes Research, 2016, Article ID: 6014631.
https://doi.org/10.1155/2016/6014631
[28]  Nguyen, T.D., Prykhodko, O., F?k H?llenius, F. and Nyman, M. (2019) Monovalerin and Trivalerin Increase Brain Acetic Acid, Decrease Liver Succinic Acid, and Alter Gut Microbiota in Rats Fed High-Fat Diets. European Journal of Nutrition, 58, 1545-1560.
https://doi.org/10.1007/s00394-018-1688-z
[29]  Faas, M.M., Liu, Y., Borghuis, T., et al. (2019) Microbiota Induced Changes in the Immune Response in Pregnant Mice. Frontiers in Immunology, 10, Article 2976.
https://doi.org/10.3389/fimmu.2019.02976
[30]  Schirmer, M., Franzosa, E.A., Lloyd-Price, J., et al. (2018) Dynamics of Metatranscription in the Inflammatory Bowel Disease Gut Microbiome. Nature Microbiology, 3, 337-346.
https://doi.org/10.1038/s41564-017-0089-z
[31]  Dong, R., Bai, M., Zhao, J., et al. (2020) A Comparative Study of the Gut Microbiota Associated with Immunoglobulin a Nephropathy and Membranous Nephropathy. Frontiers in Cellular and Infection Microbiology, 10, Article 557368.
https://doi.org/10.3389/fcimb.2020.557368
[32]  Harrison, C.A., Laubitz, D., Ohland, C.L., et al. (2018) Microbial Dysbiosis Associated with Impaired Intestinal Na+/H+ Exchange Accelerates and Exacerbates colitis in Ex-Germ Free Mice. Mucosal Immunology, 11, 1329-1341.
https://doi.org/10.1038/s41385-018-0035-2
[33]  Strati, F., Cavalieri, D., Albanese, D., et al. (2017) New Evidences on the Altered Gut Microbiota in Autism Spectrum Disorders. Microbiome, 5, Article No. 24.
https://doi.org/10.1186/s40168-017-0242-1
[34]  Gibson, G.R. (2022) Commentary on: Prebiotic Effects: Metabolic and Health Benefits. British Journal of Nutrition, 127, 554-555.
https://doi.org/10.1017/S0007114521004608
[35]  Thomas, A.M., Jesus, E.C., Lopes, A., et al. (2016) Tissue-Associated Bacterial Alterations in Rectal Carcinoma Patients Revealed by 16S rRNA Community Profiling. Frontiers in Cellular and Infection Microbiology, 6, Article 179.
https://doi.org/10.3389/fcimb.2016.00179
[36]  Hu, S., Liu, L., Chang, E.B., Wang, J.-Y. and Raufman, J.-P. (2015) Butyrate Inhibits Pro-Proliferative miR-92a by Diminishing c-Myc-Induced miR-17-92a Cluster Transcription in Human Colon Cancer Cells. Molecular Cancer, 14, Article No. 180.
https://doi.org/10.1186/s12943-015-0450-x
[37]  Bai, X., Wei, H., Liu, W., et al. (2022) Cigarette Smoke Promotes Colorectal Cancer through Modulation of Gut Microbiota and Related Metabolites. Gut, 71, 2439-2450.
https://doi.org/10.1136/gutjnl-2021-325021

Full-Text

comments powered by Disqus

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133