Gut Microbiome Phenotypes Driven by Host Genetics Affect Arsenic Metabolism

被引:64
作者
Lu, Kun [1 ,4 ]
Mahbub, Ridwan [4 ]
Cable, Peter Hans [5 ]
Ru, Hongyu [4 ]
Parry, Nicola M. A. [2 ]
Bodnar, Wanda M. [5 ]
Wishnok, John S. [1 ]
Styblo, Miroslav [5 ,6 ]
Swenberg, James A. [5 ]
Fox, James G. [1 ,2 ]
Tannenbaum, Steven R. [1 ,3 ]
机构
[1] MIT, Dept Biol Engn, Cambridge, MA 02139 USA
[2] MIT, Div Comparat Med, Cambridge, MA 02139 USA
[3] MIT, Dept Chem, Cambridge, MA 02139 USA
[4] Univ Georgia, Dept Environm Hlth Sci, Athens, GA 30602 USA
[5] Univ N Carolina, Dept Environm Sci & Engn, Chapel Hill, NC 27599 USA
[6] Univ N Carolina, Dept Nutr, Chapel Hill, NC 27599 USA
关键词
D O I
10.1021/tx400454z
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Large individual differences in susceptibility to arsenic-induced diseases are well-documented and frequently associated with different patterns of arsenic metabolism. In this context, the role of the gut microbiome in directly metabolizing arsenic and triggering systemic responses in diverse organs raises the possibility that gut microbiome phenotypes affect the spectrum of metabolized arsenic species. However, it remains unclear how host genetics and the gut microbiome interact to affect the biotransformation of arsenic. Using an integrated approach combining 16S rRNA gene sequencing and HPLC-ICP-MS arsenic speciation, we demonstrate that IL-10 gene knockout leads to a significant taxonomic change of the gut microbiome, which in turn substantially affects arsenic metabolism.
引用
收藏
页码:172 / 174
页数:3
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