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dc.contributor.authorLu, Kun
dc.contributor.authorMahbub, Ridwan
dc.contributor.authorCable, Peter Hans
dc.contributor.authorRu, Hongyu
dc.contributor.authorParry, Nicola M. A.
dc.contributor.authorBodnar, Wanda M.
dc.contributor.authorWishnok, John S.
dc.contributor.authorStyblo, Miroslav
dc.contributor.authorSwenberg, James A.
dc.contributor.authorFox, James G.
dc.contributor.authorTannenbaum, Steven Robert
dc.date.accessioned2015-04-23T18:26:57Z
dc.date.available2015-04-23T18:26:57Z
dc.date.issued2014-02
dc.date.submitted2013-12
dc.identifier.issn0893-228X
dc.identifier.issn1520-5010
dc.identifier.urihttp://hdl.handle.net/1721.1/96754
dc.description.abstractLarge 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.en_US
dc.description.sponsorshipNational Institute of Environmental Health Sciences (P30 ES010126)en_US
dc.description.sponsorshipNational Institute of Environmental Health Sciences (NIEHS grant P30 ES002109)en_US
dc.description.sponsorshipUniversity of Georgia. College of Public Health (internal grant)en_US
dc.description.sponsorshipUniversity of Georgia (Faculty Research Grant (FRG))en_US
dc.language.isoen_US
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/tx400454zen_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceAmerican Chemical Societyen_US
dc.titleGut Microbiome Phenotypes Driven by Host Genetics Affect Arsenic Metabolismen_US
dc.typeArticleen_US
dc.identifier.citationLu, Kun, Ridwan Mahbub, Peter Hans Cable, Hongyu Ru, Nicola M. A. Parry, Wanda M. Bodnar, John S. Wishnok, et al. “Gut Microbiome Phenotypes Driven by Host Genetics Affect Arsenic Metabolism.” Chemical Research in Toxicology 27, no. 2 (February 17, 2014): 172–174. © 2014 American Chemical Society.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.departmentMassachusetts Institute of Technology. Division of Comparative Medicineen_US
dc.contributor.mitauthorLu, Kunen_US
dc.contributor.mitauthorParry, Nicola M. A.en_US
dc.contributor.mitauthorWishnok, John S.en_US
dc.contributor.mitauthorFox, James G.en_US
dc.contributor.mitauthorTannenbaum, Steven Roberten_US
dc.relation.journalChemical Research in Toxicologyen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsLu, Kun; Mahbub, Ridwan; Cable, Peter Hans; Ru, Hongyu; Parry, Nicola M. A.; Bodnar, Wanda M.; Wishnok, John S.; Styblo, Miroslav; Swenberg, James A.; Fox, James G.; Tannenbaum, Steven R.en_US
dc.identifier.orcidhttps://orcid.org/0000-0002-2325-552X
dc.identifier.orcidhttps://orcid.org/0000-0001-9307-6116
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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