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Impact of enrofloxacin on the human intestinal microbiota revealed by comparative molecular analysis

机译:比较分子分析显示恩诺沙星对人体肠道菌群的影响

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The indigenous human intestinal microbiota could be disrupted by residues of antibiotics in foods as well as therapeutically administered antibiotics to humans. These disruptions may lead to adverse health outcomes. To observe the possible impact of residues of antibiotics at concentrations below therapeutic levels on human intestinal microbiota, we performed studies using in vitro cultures of fecal suspensions from three individuals with 10 different concentrations (0, 0.1, 0.5, 1, 5, 10, 15, 25, 50 and 150 μg/ml) of the fluoroquinolone, enrofloxacin. The bacterial communities of the control and enrofloxacin dosed fecal samples were analyzed by denaturing gradient gel electrophoresis (DGGE) and pyrosequencing. In addition, changes of functional gene expression were analyzed by a pyrosequencing-based random whole-community mRNA sequencing method. Although each individual had a unique microbial composition, the communities of all individuals were affected by enrofloxacin. The proportions of two phyla, namely, Bacteroidetes and Proteobacteria, were significantly reduced with increasing concentrations of enrofloxacin exposure, while the proportion of Firmicutes increased. Principal Coordinate Analysis (PCoA) using the Fast UniFrac indicated that the community structures of intestinal microbiota were shifted by enrofloxacin. Most of the mRNA transcripts and the anti-microbial drug resistance genes increased with increasing concentrations of enrofloxacin. 16S rRNA gene pyrosequencing of control and enrofloxacin treated fecal suspensions provided valuable information of affected bacterial taxa down to the species level, and the community transcriptomic analyses using mRNA revealed the functional gene expression responses of the changed bacterial communities by enrofloxacin.
机译:食物中的抗生素残留以及对人类进行治疗性施用的抗生素可能会破坏土著人的肠道微生物群。这些干扰可能导致不良的健康结果。为了观察浓度低于治疗水平的抗生素残留对人体肠道菌群的可能影响,我们进行了体外培养,研究了来自三个具有10种不同浓度(0、0.1、0.5、1、5、10、15、15、10、15、15、15、15、15、15 (25、50和150μg/ ml)的氟喹诺酮恩洛沙星。通过变性梯度凝胶电泳(DGGE)和焦磷酸测序分析对照和恩诺沙星剂量粪便样品的细菌群落。此外,通过基于焦磷酸测序的随机全社区mRNA测序方法分析功能基因表达的变化。尽管每个人都有独特的微生物组成,但每个人的社区都受到恩氟沙星的影响。随着恩诺沙星暴露浓度的增加,细菌门和变形杆菌两个门的比例显着降低,而硬毛虫的比例增加。使用快速UniFrac的主坐标分析(PCoA)表明,恩诺沙星改变了肠道菌群的群落结构。随着恩诺沙星浓度的增加,大多数mRNA转录物和抗微生物药物耐药基因均增加。对照和恩氟沙星处理的粪便悬液的16S rRNA基因焦磷酸测序提供了影响细菌菌群直至物种水平的有价值的信息,并且使用mRNA进行的转录组分析显示,恩洛沙星改变了细菌群落的功能基因表达反应。

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