The gut microbiome is required for full protection against acute arsenic toxicity in mouse models

被引:139
作者
Coryell, Michael [1 ]
McAlpine, Mark [1 ]
Pinkham, Nicholas V. [1 ]
McDermott, Timothy R. [2 ]
Walk, Seth T. [1 ]
机构
[1] Montana State Univ, Dept Microbiol & Immunol, 109 Lewis Hall, Bozeman, MT 59717 USA
[2] Montana State Univ, Dept Land Resources & Environm Sci, 637A Leon Johnson Hall, Bozeman, MT 59717 USA
基金
美国食品与农业研究所; 美国国家卫生研究院;
关键词
BUTYRATE-PRODUCING BACTERIA; INFLAMMATORY-BOWEL-DISEASE; FAECALIBACTERIUM-PRAUSNITZII; DRINKING-WATER; SEQUENCE DATA; RESISTANCE; EXPOSURE; PHYLOGROUPS; OXIDATION; ABUNDANCE;
D O I
10.1038/s41467-018-07803-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Arsenic poisons an estimated 200 million people worldwide through contaminated food and drinking water. Confusingly, the gut microbiome has been suggested to both mitigate and exacerbate arsenic toxicity. Here, we show that the microbiome protects mice from arsenic-induced mortality. Both antibiotic-treated and germ-free mice excrete less arsenic in stool and accumulate more arsenic in organs compared to control mice. Mice lacking the primary arsenic detoxification enzyme (As3mt) are hypersensitive to arsenic after antibiotic treatment or when derived germ-free, compared to wild-type and/or conventional counterparts. Human microbiome (stool) transplants protect germ-free As3mt-KO mice from arsenic-induced mortality, but protection depends on microbiome stability and the presence of specific bacteria, including Faecalibacterium. Our results demonstrate that both a functional As3mt and specific microbiome members are required for protection against acute arsenic toxicity in mouse models. We anticipate that the gut microbiome will become an important explanatory factor of disease (arsenicosis) penetrance in humans, and a novel target for prevention and treatment strategies.
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页数:9
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