评估抗生素对人类胃肠道微生物群临床前模型的影响

IF 4.6 3区 生物学 Q2 MICROBIOLOGY
Thomas A. Auchtung, Armando I. Lerma, Keegan Schuchart, Jennifer M. Auchtung
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引用次数: 0

摘要

虽然抗生素在治疗感染方面发挥着重要作用,但抗生素治疗期间胃肠道微生物群的破坏可能导致负面的健康后果。然而,对于许多抗生素来说,其活性谱是针对特定的分离物确定的,而不是针对胃肠道微生物的范围确定的。在这里,我们使用两种不同的模型系统,人类粪便微型生物反应器和人类微生物群相关小鼠,研究了胃肠道微生物群落对抗生素的反应。在使用12种不同粪便供体的微型生物反应器中建立的群落暴露于12种不同种类的抗生素。来自三个粪便供体的样本被用于定植来自三个不同遗传背景的无菌小鼠;然后将子代小鼠暴露于微型生物反应器中测试的12种抗生素中的6种。最初的细菌群落多样性取决于粪便供体和模型系统。抗生素在整个系统发育谱系中影响了广泛的类群,许多类群在不同类别的抗生素治疗中受到相似的影响。万古霉素通常用于治疗革兰氏阳性细菌感染,减少了不同分类群的丰度,包括革兰氏阴性拟杆菌群。对某些类群的影响受到模型系统的限制,表明环境背景对抗生素敏感性的重要性。总之,这些结果表明了微生物群组成和环境背景对抗生素敏感性之间的复杂相互关系,并表明了每种临床前模型系统在评估新抗生素和其他可能破坏微生物群的化合物的作用时的优缺点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Evaluating Effects of Antibiotics Across Preclinical Models of the Human Gastrointestinal Microbiota

Evaluating Effects of Antibiotics Across Preclinical Models of the Human Gastrointestinal Microbiota

While antibiotics play important roles in treating infections, disruption of the gastrointestinal microbiota during antibiotic treatment can lead to negative health consequences. However, for many antibiotics, the spectrum of activity has been determined for select isolates rather than for the range of microbes that populate the gastrointestinal tract. Here, we examined the response of communities of gastrointestinal microbes to antibiotics using two different model systems, human fecal minibioreactors and human microbiota-associated mice. Communities established in minibioreactors using 12 different fecal donors were exposed to 12 different classes of antibiotics. Samples from three fecal donors were used to colonize germ-free mice from three different genetic backgrounds; progeny mice were then exposed to 6 of 12 antibiotics tested in minibioreactors. Initial bacterial community diversity was dependent on both the fecal donor and model system. Antibiotics affected a wide range of taxa across the phylogenetic spectrum, with many taxa similarly affected across treatments with different classes of antibiotics. Vancomycin, typically administered to treat Gram-positive bacterial infections, decreased the abundance of diverse taxa, including Gram-negative Bacteroidota species. Effects on some taxa were restricted by model system, indicating the importance of environmental context on antibiotic susceptibility. Altogether, these results indicate the complex interrelationships between microbiota composition and environmental context on antibiotic susceptibility and demonstrate strengths and weaknesses of each preclinical model system for evaluating effects of new antibiotics and other compounds with potential to disrupt the microbiota.

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来源期刊
MicrobiologyOpen
MicrobiologyOpen MICROBIOLOGY-
CiteScore
8.00
自引率
0.00%
发文量
78
审稿时长
20 weeks
期刊介绍: MicrobiologyOpen is a peer reviewed, fully open access, broad-scope, and interdisciplinary journal delivering rapid decisions and fast publication of microbial science, a field which is undergoing a profound and exciting evolution in this post-genomic era. The journal aims to serve the research community by providing a vehicle for authors wishing to publish quality research in both fundamental and applied microbiology. Our goal is to publish articles that stimulate discussion and debate, as well as add to our knowledge base and further the understanding of microbial interactions and microbial processes. MicrobiologyOpen gives prompt and equal consideration to articles reporting theoretical, experimental, applied, and descriptive work in all aspects of bacteriology, virology, mycology and protistology, including, but not limited to: - agriculture - antimicrobial resistance - astrobiology - biochemistry - biotechnology - cell and molecular biology - clinical microbiology - computational, systems, and synthetic microbiology - environmental science - evolutionary biology, ecology, and systematics - food science and technology - genetics and genomics - geobiology and earth science - host-microbe interactions - infectious diseases - natural products discovery - pharmaceutical and medicinal chemistry - physiology - plant pathology - veterinary microbiology We will consider submissions across unicellular and cell-cluster organisms: prokaryotes (bacteria, archaea) and eukaryotes (fungi, protists, microalgae, lichens), as well as viruses and prions infecting or interacting with microorganisms, plants and animals, including genetic, biochemical, biophysical, bioinformatic and structural analyses. The journal features Original Articles (including full Research articles, Method articles, and Short Communications), Commentaries, Reviews, and Editorials. Original papers must report well-conducted research with conclusions supported by the data presented in the article. We also support confirmatory research and aim to work with authors to meet reviewer expectations. MicrobiologyOpen publishes articles submitted directly to the journal and those referred from other Wiley journals.
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