抗生素对小鼠结肠粘液层影响的可视化。

Ci ji yi xue za zhi = Tzu-chi medical journal Pub Date : 2019-08-20 eCollection Date: 2020-04-01 DOI:10.4103/tcmj.tcmj_70_19
Chun-Yao Chen, Kai-Chieh Hsu, Hsuan-Yu Yeh, Han-Chen Ho
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引用次数: 0

摘要

目的粘液是一道保护屏障,将敏感的上皮表面与外界隔开。小鼠结肠粘液分为无菌内层和有菌外层。众所周知,抗生素治疗会扰乱肠道微生物群,但其对粘膜屏障的影响却很少被讨论。本研究旨在评估和观察抗生素对结肠粘液和微生物群落的影响:进行了两组实验。在抗生素实验中,小鼠连续 7 天口服链霉素和杆菌肽。在恢复实验中,小鼠在接受 7 天抗生素治疗后,在不使用抗生素的情况下恢复 7 天。分离小鼠结肠并将其分为近端、中间和远端部分。在透射电子显微镜下检查标本,以确定形态变化。通过分析从小鼠结肠不同部位分离出的 16S rDNA 序列,对肠道微生物群落进行了评估:结果:经抗生素治疗的小鼠生理正常。结果:经抗生素处理的小鼠生理正常,但观察到结肠近端和中部的内粘液层明显增加,外粘液层的细菌数量急剧减少。16S rDNA 组成显示,不同结肠切片的优势类群具有相似性。对照组小鼠的微生物群多种多样,而抗生素治疗则有效地消灭了大部分细菌,因此群落中只有一种属(Toricibacter 或 Staphylococcus)占主导地位。此外,治疗后的小鼠停用抗生素后,粘液内层的厚度恢复到对照组水平,微生物群落也恢复了更复杂的结构,以固着菌、类杆菌和变形菌为主:我们的研究结果表明,抗生素治疗不仅干扰了微生物群,还改变了粘液层的结构。停用抗生素后,粘液层在几天内迅速再生,这可能是微生物生长的结果。具有不同生态作用的肠道居民(如粘蛋白降解者和发酵者)的重新定殖表明,肠道生态系统功能健全,具有很强的恢复能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Visualizing the effects of antibiotics on the mouse colonic mucus layer.

Objective: Mucus provides a protective barrier separating sensitive epithelial surfaces from the outside world. The mouse colonic mucus is organized as a bacteria-free inner layer and a bacteria-colonized outer layer. Antibiotic treatments are known to disturb gut microbiota, but their effect on the mucosal barrier is rarely discussed. The aim was to evaluate and visualize the impact of antibiotics on the colonic mucus and the microbial community.

Materials and methods: Two sets of experiments were conducted. In the antibiotic experiment, mice orally ingested both streptomycin and bacitracin for 7 days. In the recovery experiment, mice were allowed to recover for 7 days without antibiotics after having received the 7-day antibiotic treatment. Mouse colons were isolated and divided into proximal, middle, and distal parts. Specimens were examined under a transmission electron microscope to identify morphological changes. The gut microbial community was evaluated by analyzing 16S rDNA sequences isolated from the different parts of the mouse colon.

Results: The antibiotic-treated mice were physiologically normal. However, a significantly increased inner mucus layer in the proximal and middle colon and a dramatic decrease in bacterial numbers in the outer mucus layers were observed. The 16S rDNA compositions showed a similarity in the dominant taxa among different colon sections. While control mice had a diverse microbiota, antibiotic treatments effectively eliminated most of the bacteria, such that the community was dominated by only one genus (Turicibacter or Staphylococcus). Furthermore, following antibiotic withdrawal in treated mice, the thickness of the inner mucus layer returned to control levels, and the microbial community regained a more complex structure, dominated by Firmicutes, Bacteroidetes, and Proteobacteria.

Conclusions: Our results indicated that antibiotic treatments not only disturbed the microbiota but also altered the structure of the mucus layer. After the withdrawal of antibiotics, the mucus layer was quickly regenerated within days, probably in response to microbial growth. The recolonization by gut inhabitants with diverse ecological roles, such as mucin-degraders and fermenters indicate that the gut ecosystem is functionally sound and highly resilient.

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