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Monomethylmercury degradation by the human gut microbiota is stimulated by protein amendments

机译:人体肠道微生物会降解人体肠道汞的降解被蛋白质修正刺激

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Monomethylmercury (MMHg) is a potent neurotoxicant that can be bioaccumulated and biomagnified through trophic levels. Human populations whose diets contain MMHg are at risk of MMHg toxicity. The gut microbiota was identified as a potential factor causing variation in MMHg absorption and body burden. However, little is known about the role of gut microbiota on Hg transformations. We conducted a series of in vitro experiments to study the effects of dietary nutrient change on Hg metabolism and the human gut microbiota using anoxic fecal slurry incubations. We used stable Hg isotope tracers to track MMHg production and degradation and characterized the microbiota using high throughput sequencing of the 16S rRNA gene. We show that the magnitude of MMHg degradation is individual dependent and rapidly responds to changes in nutrient amendments, leading to complete degradation of the MMHg present. Although the mechanism involved remains unknown, it does not appear to involve the well-known mer operon. Our data are the first to show a nutrient dependency on the ability of the simulated human gut microbiota to demethylate MMHg. This work provides much-needed insights into individual variations in Hg absorption and potential toxicity.
机译:单甲基汞(MMHG)是一种有效的神经毒剂,可以通过营养水平进行生物累积和生物镀锌。饮食含有mmHg的人口有毒性的风险。将肠道微生物A确定为导致MMHG吸收和体重变化的潜在因素。但是,关于肠道微生物块对Hg转化的作用很​​少。我们进行了一系列体外实验,以研究饮食营养变化对Hg代谢和人体肠道微生物的影响使用缺氧粪浆液孵育。我们使用稳定的Hg同位素示踪剂来跟踪MMHG生产和降解,并使用16S rRNA基因的高通量测序表征微生物群。我们表明MMHG降解的大小是个体依赖性,迅速响应营养修正案的变化,导致存在的MMHG的劣化。虽然所涉及的机制仍然是未知的,但它似乎涉及着名的MER操纵子。我们的数据是第一个显示营养依赖性对模拟人体肠道微生物能够对去甲基化物MMHG的能力的依赖性。这项工作提供了急需的洞察力,进入HG吸收和潜在毒性的个体变化。

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