Effects of Bifidobacterium animalis subsp. lactis BB-12 and yogurt on mice during oral antibiotic administration

IF 6.1 1区 生物学 Q1 MICROBIOLOGY Microbiological research Pub Date : 2024-05-31 DOI:10.1016/j.micres.2024.127794
Ruchita G. Uttarwar , Solomon A. Mekonnen , Wannes Van Beeck , Aidong Wang , Peter Finnegan , Robert F. Roberts , Daniel Merenstein , Carolyn M. Slupsky , Maria L. Marco
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Abstract

Probiotics have the potential to prevent disruptions to normal gastrointestinal function caused by oral antibiotic use. In this study, we examined the capacity of Bifidobacterium animalis subspecies lactis BB-12 (BB-12) and yogurt, separately and combined, to mitigate the effects of the antibiotic amoxicillin-clavulanate (AMC) on the gut microbiota and metabolomes of C57BL/6 J mice. Male and female mice were administered either BB-12, yogurt, BB-12 in yogurt, or saline for 10 days concurrent with the inclusion of AMC in the drinking water. Male mice exposed to AMC exhibited significant reductions (p<0.05) in body weight over the course of the study compared to sham (no AMC) controls whereas no such effects were observed for female mice. AMC administration resulted in rapid alterations to the intestinal microbiota in both sexes irrespective of BB-12 or yogurt treatment, including significant (p<0.05) losses in bacterial cell numbers and changes in microbial alpha-diversity and beta-diversity in the feces and cecal contents. The effects of AMC on the gut microbiota were observed within one day of administration and the bacterial contents continued to change over time, showing a succession marked by rapid reductions in Muribaculaceae and Lachnospiraceae and temporal increases in proportions of Acholeplasmataceae (day 1) and Streptococcaceae and Leuconostocaceae (day 5). By day 10 of AMC intake, high proportions of Gammaproteobacteria assigned as Erwiniaceae or Enterobacteriaceae (average of 63 %), were contained in the stools and were similarly enriched in the cecum. The cecal contents of mice given AMC harbored significantly reduced concentrations of (branched) short-chain fatty acids (SCFA), aspartate, and other compounds, whereas numerous metabolites, including formate, lactate, and several amino acids and amino acid derivatives were significantly enriched. Despite the extensive impact of AMC, starting at day 7 of the study, the body weights of male mice given yogurt or BB-12 (in saline) with AMC were similar to the healthy controls. BB-12 (in saline) and yogurt intake was associated with increased Streptococcaceae and both yogurt and BB-12 resulted in lower proportions of Erwiniaceae in the fecal and cecal contents. The cecal contents of mice fed BB-12 in yogurt contained levels of formate, glycine, and glutamine that were equivalent to the sham controls. These findings highlight the potential of BB-12 and yogurt to mitigate antibiotic-induced gut dysbiosis.

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口服抗生素期间动物双歧杆菌亚种 BB-12 和酸奶对小鼠的影响
益生菌具有防止口服抗生素对正常胃肠功能造成破坏的潜力。在这项研究中,我们检测了动物双歧杆菌亚种乳杆菌 BB-12(BB-12)和酸奶单独或联合使用对减轻抗生素阿莫西林-克拉维酸(AMC)对 C57BL/6 J 小鼠肠道微生物群和代谢组影响的能力。在饮用水中加入 AMC 的同时,雄性和雌性小鼠分别服用 BB-12、酸奶、酸奶中的 BB-12 或生理盐水 10 天。在研究过程中,与假对照组(不含 AMC)相比,暴露于 AMC 的雄性小鼠体重显著下降(p<0.05),而雌性小鼠则没有观察到这种影响。无论BB-12或酸奶处理与否,给雌雄小鼠服用AMC都会导致肠道微生物群迅速发生变化,包括细菌细胞数量的显著减少(p<0.05)以及粪便和盲肠内容物中微生物α-多样性和β-多样性的变化。AMC对肠道微生物群的影响在给药后一天内就可观察到,随着时间的推移,细菌含量持续发生变化,表现出一种连续性,其特点是Muribaculaceae和Lachnospiraceae迅速减少,Acholeplasmataceae(第1天)和Streptococcaceae和Leuconostocaceae(第5天)的比例随时间增加。到摄入 AMC 的第 10 天,粪便中含有大量被归类为 Erwiniaceae 或 Enterobacteriaceae 的 Gammaproteobacteria(平均为 63%),盲肠中的含量也同样丰富。服用 AMC 的小鼠盲肠内容物中的(支链)短链脂肪酸 (SCFA)、天门冬氨酸和其他化合物的浓度明显降低,而包括甲酸盐、乳酸盐、多种氨基酸和氨基酸衍生物在内的多种代谢物的浓度则明显增高。尽管 AMC 产生了广泛的影响,但从研究的第 7 天开始,雄性小鼠饮用酸奶或 BB-12(生理盐水)后的体重与健康对照组相似。BB-12(生理盐水)和酸奶的摄入量与链球菌的增加有关,而酸奶和BB-12都会导致粪便和盲肠内容物中的埃文菌科比例降低。在酸奶中添加 BB-12 的小鼠盲肠内容物中甲酸盐、甘氨酸和谷氨酰胺的含量与假对照组相当。这些发现凸显了 BB-12 和酸奶缓解抗生素引起的肠道菌群失调的潜力。
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来源期刊
Microbiological research
Microbiological research 生物-微生物学
CiteScore
10.90
自引率
6.00%
发文量
249
审稿时长
29 days
期刊介绍: Microbiological Research is devoted to publishing reports on prokaryotic and eukaryotic microorganisms such as yeasts, fungi, bacteria, archaea, and protozoa. Research on interactions between pathogenic microorganisms and their environment or hosts are also covered.
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