The Celiac Center, Division of Gastroenterology; Beth Israel Deaconess Medical Center; Harvard Medical School; Boston, MA USA.
Molecular Research LP; Shallowater, TX USA.
Gut Microbes. 2014 Jul 1;5(4):458-67. doi: 10.4161/gmic.29558. Epub 2014 Jul 9.
Interactions between the microbial flora of the intestine and the human host play a critical role inmaintaining intestinal health and in the pathophysiology of a wide variety of disorders such as antibiotic associated diarrhea, Clostridium difficile infection, and inflammatory bowel disease. Prebiotics can confer health benefits by beneficial effects on the intestinal microbiome, whereas antibiotics can disrupt the microbiome leading to diarrhea andother side effects.
To compare the effects of the prebiotic, polysaccharopeptide from Trametes versicolor, to those of the antibiotic,amoxicillin, on the human gut microbiome
Twenty-four healthy volunteers were randomized to receive PSP, amoxicillin, or no treatment (control).Stool specimens were analyzed using bTEFAP microbial ecology methods on seven occasions over 8 weeks from each participant in the active treatment groups and on three occasions for the controls.
Twenty-two of 24 participants completed the protocol. PSP led to clear and consistent microbiome changes consistent with its activity as a prebiotic. Despite the diversity of the human microbiome we noted strong microbiome clustering among subjects. Baseline microbiomes tended to remain stable and to overshadow the treatment effects.Amoxicillin treatment caused substantial microbiome changes most notably an increase in Escherichia/Shigella. Antibiotic associated changes persisted to the end of the study, 42 days after antibiotic therapy ended.
The microbiomes of healthy individuals show substantial diversity but remain stable over time.The antibiotic amoxicillin alters the microbiome and recovery from this disruption can take several weeks. PSP from T. versicolor acts as a prebiotic to modulate human intestinal microbiome composition.
肠道微生物群与人类宿主之间的相互作用在维持肠道健康以及多种疾病的病理生理学方面发挥着关键作用,如抗生素相关性腹泻、艰难梭菌感染和炎症性肠病。益生元可以通过对肠道微生物组的有益影响来带来健康益处,而抗生素会破坏微生物组,导致腹泻和其他副作用。
比较真菌云芝多糖(PSP)作为一种益生元与抗生素阿莫西林对人类肠道微生物组的影响。
将 24 名健康志愿者随机分为 PSP、阿莫西林或不治疗(对照)组。在 8 周的时间内,对活性治疗组的每位参与者进行了 7 次,对对照组进行了 3 次粪便样本分析,使用 bTEFAP 微生物生态学方法。
24 名参与者中的 22 名完成了方案。PSP 导致了明显且一致的微生物组变化,这与它作为益生元的作用一致。尽管人类微生物组具有多样性,但我们注意到受试者之间存在强烈的微生物组聚类。基线微生物组趋于稳定,并掩盖了治疗效果。阿莫西林治疗导致了显著的微生物组变化,特别是大肠杆菌/志贺氏菌的增加。抗生素相关的变化持续到研究结束,即抗生素治疗结束后 42 天。
健康个体的微生物组显示出很大的多样性,但随着时间的推移保持稳定。抗生素阿莫西林改变了微生物组,从这种破坏中恢复可能需要数周时间。云芝真菌多糖(T. versicolor)作为一种益生元,可以调节人类肠道微生物组的组成。