抗生素治疗后牦牛地衣芽孢杆菌对小鼠模型的影响。

IF 3.9 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Applied Microbiology and Biotechnology Pub Date : 2024-12-01 Epub Date: 2024-01-16 DOI:10.1007/s00253-023-12866-w
Zhibo Zeng, Saisai Gong, Chuxian Quan, Shimeng Zhou, Muhammad Fakhar-E-Alam Kulyar, Mudassar Iqbal, Yan Li, Xiang Li, Jiakui Li
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The result showed that A group (antibiotic treatment) significantly reduced body weight and decreased the length of jejunal intestinal villi and the villi to crypt (V/C) value, which also caused structural damage to the jejunal mucosa. Meanwhile, antibiotic treatment suppressed the mRNA expression of tight junction proteins ZO-1, claudin, occludin, and Ki67 and elevated MUC2 expression more than the other Groups (P < 0.05 and P < 0.01). However, T group (B. licheniformis supplements after antibiotic treatment) restored the expression of the above genes, and there was no statistically significant difference compared to the control group (P > 0.05). Moreover, the antibiotic treatment increased the relative abundance of 4 bacterial phyla affiliated with 16 bacterial genera in the jejunum community, including the dominant Firmicutes, Proteobacteria, and Cyanobacteria in the jejunum. 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引用次数: 0

摘要

肠道微生物(GM)是宿主微生物组和健康系统不可或缺的组成部分。滥用抗生素会破坏微生物组的平衡,影响环境病原体和宿主相关细菌。然而,有关地衣芽孢杆菌减轻抗生素不良影响的研究相对较少。为了测试地衣芽孢杆菌作为益生菌补充剂对抗生素影响的作用,研究人员应用头孢氨苄,通过病理学、实时 PCR(RT-PCR)和高通量测序(HTS)研究了头孢氨苄引起的空肠群落紊乱和肠屏障损伤的恢复情况。结果表明,A组(抗生素治疗)体重明显降低,空肠绒毛长度和绒毛与隐窝比值(V/C)明显降低,空肠黏膜结构也受到破坏;B组(抗生素治疗)体重明显降低,空肠绒毛长度和绒毛与隐窝比值(V/C)明显降低,空肠黏膜结构也受到破坏。同时,与其他组相比,抗生素治疗抑制了紧密连接蛋白 ZO-1、claudin、occludin 和 Ki67 的 mRNA 表达,并升高了 MUC2 的表达(P < 0.05 和 P < 0.01)。然而,T 组(抗生素治疗后补充地衣芽孢杆菌)恢复了上述基因的表达,与对照组相比无统计学差异(P > 0.05)。此外,抗生素处理增加了空肠群落中 4 个细菌门、16 个细菌属的相对丰度,包括空肠中占优势的固缩菌、变形菌和蓝细菌。抗生素治疗后补充地衣芽孢杆菌会降低类杆菌和变形菌的相对丰度,增加固缩菌、Epsilonbacteraeota、乳酸杆菌和Candidatus Stoquefichus的相对丰度。这项研究通过考虑与环境抗生素污染水平相关的暴露浓度和持续时间,模拟了真实世界的暴露情景。我们描述了使用地衣芽孢杆菌进行抗生素治疗后可恢复肠道微生物群紊乱并修复肠道屏障。要点:地衣芽孢杆菌抗生素后治疗- 地衣芽孢杆菌抗生素后可恢复肠道平衡、修复肠道屏障并有助于健康 - 抗生素会损害肠道屏障、改变结构并增加疾病风险 - 长期服用抗生素会影响肠道并增加疾病易感性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Impact of Bacillus licheniformis from yaks following antibiotic therapy in mouse model.

Impact of Bacillus licheniformis from yaks following antibiotic therapy in mouse model.

Gut microorganism (GM) is an integral component of the host microbiome and health system. Abuse of antibiotics disrupts the equilibrium of the microbiome, affecting environmental pathogens and host-associated bacteria alike. However, relatively little research on Bacillus licheniformis alleviates the adverse effects of antibiotics. To test the effect of B. licheniformis as a probiotic supplement against the effects of antibiotics, cefalexin was applied, and the recovery from cefalexin-induced jejunal community disorder and intestinal barrier damage was investigated by pathology, real-time PCR (RT-PCR), and high-throughput sequencing (HTS). The result showed that A group (antibiotic treatment) significantly reduced body weight and decreased the length of jejunal intestinal villi and the villi to crypt (V/C) value, which also caused structural damage to the jejunal mucosa. Meanwhile, antibiotic treatment suppressed the mRNA expression of tight junction proteins ZO-1, claudin, occludin, and Ki67 and elevated MUC2 expression more than the other Groups (P < 0.05 and P < 0.01). However, T group (B. licheniformis supplements after antibiotic treatment) restored the expression of the above genes, and there was no statistically significant difference compared to the control group (P > 0.05). Moreover, the antibiotic treatment increased the relative abundance of 4 bacterial phyla affiliated with 16 bacterial genera in the jejunum community, including the dominant Firmicutes, Proteobacteria, and Cyanobacteria in the jejunum. B. licheniformis supplements after antibiotic treatment reduced the relative abundance of Bacteroidetes and Proteobacteria and increased the relative abundance of Firmicutes, Epsilonbacteraeota, Lactobacillus, and Candidatus Stoquefichus. This study uses mimic real-world exposure scenarios by considering the concentration and duration of exposure relevant to environmental antibiotic contamination levels. We described the post-antibiotic treatment with B. licheniformis could restore intestinal microbiome disorders and repair the intestinal barrier. KEY POINTS: • B. licheniformis post-antibiotics restore gut balance, repair barrier, and aid health • Antibiotics harm the gut barrier, alter structure, and raise disease risk • Long-term antibiotics affect the gut and increase disease susceptibility.

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来源期刊
Applied Microbiology and Biotechnology
Applied Microbiology and Biotechnology 工程技术-生物工程与应用微生物
CiteScore
10.00
自引率
4.00%
发文量
535
审稿时长
2 months
期刊介绍: Applied Microbiology and Biotechnology focusses on prokaryotic or eukaryotic cells, relevant enzymes and proteins; applied genetics and molecular biotechnology; genomics and proteomics; applied microbial and cell physiology; environmental biotechnology; process and products and more. The journal welcomes full-length papers and mini-reviews of new and emerging products, processes and technologies.
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