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HNU082对大肠和小肠中微生物单核苷酸变异的不同影响。

Distinct Effects of HNU082 on Microbial Single-Nucleotide Variants in Large Intestine and Small Intestine.

作者信息

Ma Wenyao, Han Zhe, Liu Xinlei, Cui Weipeng, Zhen Dongyu, Zhou Xiaolu, Song Yuan, Jiang Shuaiming

机构信息

Key Laboratory of Food Nutrition and Functional Food of Hainan Province, School of Food Science and Engineering, Hainan University, Haikou 570228, China.

出版信息

Microorganisms. 2025 Mar 25;13(4):731. doi: 10.3390/microorganisms13040731.

DOI:10.3390/microorganisms13040731
PMID:40284568
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12029867/
Abstract

The intestinal tract extends several times the length of bodies, with varying environmental conditions across different segments (small intestinal and large intestinal), thereby harboring distinct gut microbiota. Most studies focused on the quantitative responses of gut microbiota upon probiotics entering the gut, without an in-depth analysis of how the genetic change in local gut microbiota. Therefore, in this experiment, C57BL/6J male mice were once administered HNU082 (Lp082). Then, the mice were euthanized on the 1st, 3rd, and 7th days after gavage, and the contents of the small and large intestines of the mice were scraped for metagenomic analysis. Based on the characterization of large intestine and small intestine bacteria, changes in the diversity and abundance of single-nucleotide variants (SNVs) of microbiota were analyzed. There were observable distinct responses at the genetic level. A significant number of SNVs were identified in in the large intestine. These SNVs may impact the utilization of carbohydrates in . Ingested probiotics traversed the entire gut and interacted with the indigenous microbiota, driving the evolution of the indigenous gut microbiota in the different intestinal segments, thereby influencing microbial growth and metabolism. This study investigates the role of probiotics in the evolution of gut microbiota. It offers new probiotic insights and a basis for targeted interventions.

摘要

肠道的长度是身体长度的数倍,不同节段(小肠和大肠)的环境条件各异,因而拥有不同的肠道微生物群。大多数研究聚焦于益生菌进入肠道后肠道微生物群的定量反应,而未深入分析局部肠道微生物群的基因变化情况。因此,在本实验中,对C57BL/6J雄性小鼠一次性给予HNU082(Lp082)。然后,在灌胃后的第1天、第3天和第7天对小鼠实施安乐死,并刮取小鼠小肠和大肠内容物进行宏基因组分析。基于大肠和小肠细菌的特征,分析了微生物群单核苷酸变异(SNV)的多样性和丰度变化。在基因水平上观察到了明显不同的反应。在大肠中鉴定出了大量的SNV。这些SNV可能会影响[此处原文缺失相关内容]中碳水化合物的利用。摄入的益生菌穿过整个肠道并与本土微生物群相互作用,推动不同肠道节段中本土肠道微生物群的进化,从而影响微生物的生长和代谢。本研究探讨了益生菌在肠道微生物群进化中的作用。它为靶向干预提供了新的益生菌见解和依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39cb/12029867/0db0abda4888/microorganisms-13-00731-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39cb/12029867/a3b008ad7a55/microorganisms-13-00731-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39cb/12029867/205ed3b3dad4/microorganisms-13-00731-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39cb/12029867/f3f4d4b4eb90/microorganisms-13-00731-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39cb/12029867/e4f0018a3cf9/microorganisms-13-00731-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39cb/12029867/d4deacf45548/microorganisms-13-00731-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39cb/12029867/a5a428c49456/microorganisms-13-00731-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39cb/12029867/0db0abda4888/microorganisms-13-00731-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39cb/12029867/a3b008ad7a55/microorganisms-13-00731-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39cb/12029867/205ed3b3dad4/microorganisms-13-00731-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39cb/12029867/f3f4d4b4eb90/microorganisms-13-00731-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39cb/12029867/e4f0018a3cf9/microorganisms-13-00731-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39cb/12029867/d4deacf45548/microorganisms-13-00731-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39cb/12029867/a5a428c49456/microorganisms-13-00731-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39cb/12029867/0db0abda4888/microorganisms-13-00731-g007.jpg

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本文引用的文献

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Establishing a novel inflammatory bowel disease prediction model based on gene markers identified from single nucleotide variants of the intestinal microbiota.基于从肠道微生物群单核苷酸变异中鉴定出的基因标记建立一种新型炎症性肠病预测模型。
Imeta. 2022 Jul 24;1(3):e40. doi: 10.1002/imt2.40. eCollection 2022 Sep.
2
Microbiota metabolism of intestinal amino acids impacts host nutrient homeostasis and physiology.肠道氨基酸的微生物代谢影响宿主营养稳态和生理机能。
Cell Host Microbe. 2024 May 8;32(5):661-675.e10. doi: 10.1016/j.chom.2024.04.004. Epub 2024 Apr 23.
3
A theory-informed emotion regulation variability index: Bray-Curtis dissimilarity.
一个基于理论的情绪调节变异性指数:布雷-柯蒂斯差异度
Emotion. 2024 Aug;24(5):1273-1285. doi: 10.1037/emo0001344. Epub 2024 Feb 15.
4
Microbial-derived imidazole propionate links the heart failure-associated microbiome alterations to disease severity.微生物衍生的咪唑丙酸将与心力衰竭相关的微生物组改变与疾病严重程度联系起来。
Genome Med. 2024 Feb 8;16(1):27. doi: 10.1186/s13073-024-01296-6.
5
Cross-cohort single-nucleotide-variant profiling of gut microbiota suggests a novel gut-health assessment approach.跨队列单核苷酸变异体分析肠道微生物群提示了一种新的肠道健康评估方法。
mSystems. 2023 Dec 21;8(6):e0082823. doi: 10.1128/msystems.00828-23. Epub 2023 Oct 31.
6
Native microbiome dominates over host factors in shaping the probiotic genetic evolution in the gut.本土微生物组在塑造肠道益生菌遗传进化方面占据主导地位,超过宿主因素的影响。
NPJ Biofilms Microbiomes. 2023 Oct 14;9(1):80. doi: 10.1038/s41522-023-00447-8.
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Multimodal metagenomic analysis reveals microbial single nucleotide variants as superior biomarkers for early detection of colorectal cancer.多模态宏基因组分析显示微生物单核苷酸变异作为结直肠癌早期检测的优异生物标志物。
Gut Microbes. 2023 Dec;15(2):2245562. doi: 10.1080/19490976.2023.2245562.
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The gut microbes in inflammatory bowel disease: Future novel target option for pharmacotherapy.炎症性肠病中的肠道微生物:药物治疗的未来新型靶向选择。
Biomed Pharmacother. 2023 Sep;165:114893. doi: 10.1016/j.biopha.2023.114893. Epub 2023 Jun 21.
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Single nucleotide variants in populations from sputum correlate with baseline lung function and predict disease progression in individuals with cystic fibrosis.人群中的单核苷酸变异与基线肺功能相关,并可预测囊性纤维化患者的疾病进展。
Microb Genom. 2023 Apr;9(4). doi: 10.1099/mgen.0.000981.
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The Interplay of Dietary Fibers and Intestinal Microbiota Affects Type 2 Diabetes by Generating Short-Chain Fatty Acids.膳食纤维与肠道微生物群的相互作用通过产生短链脂肪酸影响2型糖尿病。
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