Fecal Microbiota Transplantation Decreases Intestinal Loads of Multi-Drug Resistant Pseudomonas aeruginosa in Murine Carriers.

European Journal of Microbiology & Immunology Pub Date : 2019-03-04 eCollection Date: 2019-03-18 DOI:10.1556/1886.2019.00002
Katharina Mrazek, Stefan Bereswill, Markus M Heimesaat
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引用次数: 5

Abstract

Intestinal carriage of multi-drug resistant (MDR) Gram-negative bacteria including Pseudomonas aeruginosa (Psae) constitutes a pivotal prerequisite for subsequent fatal endogenous infections in patients at risk. We here addressed whether fecal microbiota transplantation (FMT) could effectively combat MDR-Psae carriage. Therefore, secondary abiotic mice were challenged with MDR-Psae by gavage. One week later, mice were subjected to peroral FMT from either murine or human donors on 3 consecutive days. Irrespective of murine or human origin of fecal transplant, intestinal MDR-Psae loads decreased as early as 24 h after the initial FMT. Remarkably, the murine FMT could lower intestinal MDR-Psae burdens by approximately 4 log orders of magnitude within 1 week. In another intervention study, mice harboring a human gut microbiota were perorally challenged with MDR-Psae and subjected to murine FMT on 3 consecutive days, 1 week later. Strikingly, within 5 days, murine FMT resulted in lower loads and carrier rates of MDR-Psae in mice with a human gut microbiota. In conclusion, FMT might be a promising antibiotics-independent option to combat intestinal MDR-Psae carriage and thus prevent from future endogenous infections of patients at risk.

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粪便菌群移植降低小鼠多重耐药铜绿假单胞菌携带者肠道负荷。
包括铜绿假单胞菌(Psae)在内的多重耐药(MDR)革兰氏阴性细菌的肠道携带是高危患者随后发生致命内源性感染的关键先决条件。我们在这里讨论了粪便微生物群移植(FMT)是否可以有效地对抗耐多药psae的携带。因此,采用灌胃法对继发性非生物小鼠进行耐多药psae攻击。一周后,小鼠连续3天接受来自小鼠或人类供体的口腔FMT。无论粪便移植的来源是鼠还是人,肠道耐多药psae负荷早在首次FMT后24小时就下降了。值得注意的是,小鼠FMT可在1周内将肠道MDR-Psae负担降低约4个对数数量级。在另一项干预研究中,携带人类肠道微生物群的小鼠在1周后连续3天口服耐多药psae并接受小鼠FMT。引人注目的是,在5天内,小鼠FMT导致具有人类肠道微生物群的小鼠中耐多药psae的负荷和携带者率降低。总之,FMT可能是对抗肠道耐多药psae携带的一种有前景的不依赖抗生素的选择,从而防止未来有内源性感染风险的患者。
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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