Ishizawa Kota, Tamahara Toru, Suzuki Suguo, Hatayama Yutaka, Li Bin, Abe Michiaki, Aoki Yuichi, Arita Ryutaro, Saito Natsumi, Ohsawa Minoru, Kaneko Soichiro, Ono Rie, Takayama Shin, Shimada Muneaki, Kumada Kazuki, Koike Tomoyuki, Masamune Atsushi, Onodera Ko, Ishii Tadashi, Shimizu Ritsuko, Kanno Takeshi
Department of Education and Support for Regional Medicine, Tohoku University Hospital, Sendai 980-8574, Japan.
Tohoku Medical Megabank Organization, Tohoku University, Sendai 980-8573, Japan.
Microorganisms. 2024 Jun 28;12(7):1324. doi: 10.3390/microorganisms12071324.
The gastrointestinal (GI) tract harbors trillions of microorganisms known to influence human health and disease, and next-generation sequencing (NGS) now enables the in-depth analysis of their diversity and functions. Although a significant amount of research has been conducted on the GI microbiome, comprehensive metagenomic datasets covering the entire tract are scarce due to cost and technical challenges. Despite the widespread use of fecal samples, integrated datasets encompassing the entire digestive process, beginning at the mouth and ending with feces, are lacking. With this study, we aimed to fill this gap by analyzing the complete metagenome of the GI tract, providing insights into the dynamics of the microbiota and potential therapeutic avenues. In this study, we delved into the complex world of the GI microbiota, which we examined in five healthy Japanese subjects. While samples from the whole GI flora and fecal samples provided sufficient bacteria, samples obtained from the stomach and duodenum posed a challenge. Using a principal coordinate analysis (PCoA), clear clustering patterns were identified; these revealed significant diversity in the duodenum. Although this study was limited by its small sample size, the flora in the overall GI tract showed unwavering consistency, while the duodenum exhibited unprecedented phylogenetic diversity. A visual heat map illustrates the discrepancy in abundance, with Fusobacteria and dominating the upper GI tract and and dominating the fecal samples. and were found throughout the digestive tract. This study demonstrates that it is possible to continuously collect microbiome samples throughout the human digestive tract. These findings not only shed light on the complexity of GI microbiota but also provide a basis for future research.
胃肠道中栖息着数万亿微生物,已知这些微生物会影响人类健康和疾病,而新一代测序(NGS)技术如今能够对其多样性和功能进行深入分析。尽管已经对胃肠道微生物组进行了大量研究,但由于成本和技术挑战,涵盖整个胃肠道的全面宏基因组数据集仍然稀缺。尽管粪便样本被广泛使用,但缺乏从口腔开始到粪便结束涵盖整个消化过程的综合数据集。在本研究中,我们旨在通过分析胃肠道的完整宏基因组来填补这一空白,从而深入了解微生物群的动态变化以及潜在的治疗途径。在这项研究中,我们深入探究了胃肠道微生物群这个复杂的领域,对五名健康的日本受试者进行了检查。虽然来自整个胃肠道菌群的样本和粪便样本提供了足够的细菌,但从胃和十二指肠获取样本却面临挑战。通过主坐标分析(PCoA),我们识别出了清晰的聚类模式;这些模式揭示了十二指肠中存在显著的多样性。尽管这项研究受样本量小的限制,但整个胃肠道中的菌群表现出了稳定的一致性,而十二指肠则展现出了前所未有的系统发育多样性。一张直观的热图展示了丰度上的差异,其中梭杆菌在胃肠道上部占主导,而拟杆菌和厚壁菌在粪便样本中占主导。变形菌在整个消化道中都有发现。这项研究表明,有可能在整个人类消化道中持续收集微生物组样本。这些发现不仅揭示了胃肠道微生物群的复杂性,也为未来的研究提供了基础。