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微生物群的空间变异:驴不同肠道段和粪便中微生物组成及预测功能的比较分析

Spatial variations in the microbiota: comparative analysis of microbial composition and predicted functions across different intestinal segments and feces in donkeys.

作者信息

Wang Yanwei, Hu Tong, Liang Kaixuan, Li Shinuo, Zhang Qiyue, Li Wenqiang, Qu Honglei, Dong Boying, Zhang Haihua, Ma Qiugang, Jia Ru, Huang Shimeng

机构信息

Food Processing and Safety, College of Life Sciences, Shanxi University, Taiyuan, China.

National Key Laboratory of Livestock and Poultry Nutrition and Feeding, College of Animal Science and Technology, China Agricultural University, Beijing, China.

出版信息

Front Microbiol. 2025 Jan 17;15:1494926. doi: 10.3389/fmicb.2024.1494926. eCollection 2024.

DOI:10.3389/fmicb.2024.1494926
PMID:39895934
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11782143/
Abstract

Donkeys, as single-stomach herbivores, have a complex and diverse microbial community in their digestive tracts. The intestinal bacterial community is crucial for maintaining intestinal homeostasis, as well as the host's overall nutrition and health. However, research on donkey gut microbes is relatively limited, particularly regarding the microbial colonization patterns in different intestinal segments of adult donkeys. Therefore, this study examined the abundance and function of microbiota across various sites of the intestinal tract (duodenum, jejunum, ileum, cecum, colon) and feces of healthy adult Dezhou male donkeys using 16S rRNA gene sequencing and PICRUSt analysis. The results indicate that donkeys have a rich gut microbial diversity and a large microbial population. No significant differences in the indices of alpha diversity were observed among the donkey's duodenum, jejunum, ileum, cecum, colon, and feces. A Venn diagram analysis revealed the presence of both unique (Duodenum: 4645; Jejunum: 3586; Ileum: 4904; Cecum: 4253; Colon: 6135; Feces: 4885) and shared (339) ASVs among the different sections. A principal coordinate analysis (PCoA) revealed significant differences (R = 0.2076,  < 0.007) across the six intestinal segments of the donkeys. At the phylum level, Firmicutes (63.64%), Bacteroidetes (20.72%), Verrucomicrobiota (9.16%), Patescibacteria (1.95%), Spirochaetota (1.87%), Actinobacteriota (1.13%), and Proteobacteria (0.42%) were the dominant bacteria in all samples. The Wilcoxon rank-sum test revealed significant differences in the proportions of genera among different intestinal segments. Specific genera were significantly enriched in various segments: and in the duodenum; and in the jejunum; and in the ileum; and in the cecum; and in the colon; and and in the feces. A PICRUSt2 functional prediction analysis indicated that carbohydrate metabolism, prokaryotic cellular communities, antimicrobial drug resistance, immune diseases, membrane transport, signal transduction, and transcription exhibited significant differences among the different intestinal segments. This study provided critical primary data on the differences in donkey gut microbiota and the synergistic effects between gut microbiota and host functions. These findings can be used to assess donkey health status, improve breeding, and develop microbial additives.

摘要

驴作为单胃草食动物,其消化道中存在复杂多样的微生物群落。肠道细菌群落对于维持肠道内环境稳定以及宿主的整体营养和健康至关重要。然而,关于驴肠道微生物的研究相对有限,尤其是成年驴不同肠道段的微生物定植模式。因此,本研究采用16S rRNA基因测序和PICRUSt分析,检测了健康成年德州雄性驴肠道各部位(十二指肠、空肠、回肠、盲肠、结肠)和粪便中微生物群的丰度和功能。结果表明,驴具有丰富的肠道微生物多样性和庞大的微生物种群。在驴的十二指肠、空肠、回肠、盲肠、结肠和粪便中,α多样性指数未观察到显著差异。Venn图分析显示不同肠段中存在独特的(十二指肠:4645;空肠:3586;回肠:4904;盲肠:4253;结肠:6135;粪便:4885)和共享的(339)可操作分类单元(ASVs)。主坐标分析(PCoA)显示驴的六个肠道段之间存在显著差异(R = 0.2076, < 0.007)。在门水平上,厚壁菌门(63.64%)、拟杆菌门(20.72%)、疣微菌门(9.16%)、Patescibacteria(1.95%)、螺旋体门(1.87%)、放线菌门(1.13%)和变形菌门(0.42%)是所有样本中的优势菌。Wilcoxon秩和检验显示不同肠道段中属的比例存在显著差异。特定的属在不同肠段中显著富集:十二指肠中为 和 ;空肠中为 和 ;回肠中为 和 ;盲肠中为 和 ;结肠中为 和 ;粪便中为 和 。PICRUSt2功能预测分析表明,碳水化合物代谢、原核细胞群落、抗菌药物抗性、免疫疾病、膜转运、信号转导和转录在不同肠道段之间存在显著差异。本研究提供了关于驴肠道微生物群差异以及肠道微生物群与宿主功能之间协同作用的关键基础数据。这些发现可用于评估驴的健康状况、改善养殖以及开发微生物添加剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fdf/11782143/86931392f4c3/fmicb-15-1494926-g009.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fdf/11782143/86931392f4c3/fmicb-15-1494926-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fdf/11782143/b924c8306e19/fmicb-15-1494926-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fdf/11782143/5a101b59f336/fmicb-15-1494926-g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fdf/11782143/181320e162e0/fmicb-15-1494926-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fdf/11782143/bb70fd9e8a3c/fmicb-15-1494926-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fdf/11782143/e48d74415f05/fmicb-15-1494926-g007.jpg
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