ADAMOVSKÝ, Ondřej, Amanda N. BUERGER, Hana VESPALCOVÁ, Shahadur R. SOHAG, Amy T. HANLON, Pamela E. GINN, Serena L. CRAFT, Stanislav SMATANA, Eva BUDINSKÁ, Maria PERSICO, Joseph H., Jr. BISESI and Christopher J. MARTYNIUK. Evaluation of Microbiome-Host Relationships in the Zebrafish Gastrointestinal System Reveals Adaptive Immunity Is a Target of Bis(2-ethylhexyl) Phthalate (DEHP) Exposure. Technology. Washington, D.C.: American Chemical Society, 2020, vol. 54, No 9, p. 5719-5728. ISSN 0013-936X. Available from: https://dx.doi.org/10.1021/acs.est.0c00628.
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Original name Evaluation of Microbiome-Host Relationships in the Zebrafish Gastrointestinal System Reveals Adaptive Immunity Is a Target of Bis(2-ethylhexyl) Phthalate (DEHP) Exposure
Authors ADAMOVSKÝ, Ondřej (203 Czech Republic, belonging to the institution), Amanda N. BUERGER (840 United States of America), Hana VESPALCOVÁ (203 Czech Republic, belonging to the institution), Shahadur R. SOHAG (840 United States of America), Amy T. HANLON (840 United States of America), Pamela E. GINN (840 United States of America), Serena L. CRAFT (840 United States of America), Stanislav SMATANA (703 Slovakia, belonging to the institution), Eva BUDINSKÁ (703 Slovakia, guarantor, belonging to the institution), Maria PERSICO (380 Italy, belonging to the institution), Joseph H., Jr. BISESI (840 United States of America) and Christopher J. MARTYNIUK (840 United States of America).
Edition Technology, Washington, D.C. American Chemical Society, 2020, 0013-936X.
Other information
Original language English
Type of outcome Article in a journal
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
WWW URL
RIV identification code RIV/00216224:14310/20:00116075
Organization Přírodovědecká fakulta – Repository – Repository
Doi http://dx.doi.org/10.1021/acs.est.0c00628
UT WoS 000530651900046
Keywords in English DI(2-ETHYLHEXYL) PHTHALATE; AIRWAY INFLAMMATION; INTESTINAL FAILURE; ENTEROCYTE MASS; TIGHT JUNCTIONS; CELLS; NEUROPEPTIDES; ASSOCIATIONS; CITRULLINE; EXPRESSION
Links EF17_043/0009632, research and development project. LM2015085, research and development project. LM2018121, research and development project. 707241, interní kód Repo. 857560, interní kód Repo. CESNET II, large research infrastructures.
Changed by Changed by: RNDr. Daniel Jakubík, učo 139797. Changed: 25/1/2022 14:10.
Abstract
To improve physical characteristics of plastics such as flexibility and durability, producers enrich materials with phthalates such as di-2-(ethylhexyl) phthalate (DEHP). DEHP is a high production volume chemical associated with metabolic and immune disruption in animals and humans. To reveal mechanisms implicated in phthalate-related disruption in the gastrointestinal system, male and female zebrafish were fed DEHP (3 ppm) daily for two months. At the transcriptome level, DEHP significantly upregulated gene networks in the intestine associated with helper T cells' (Th1, Th2, and Th17) specific pathways. The activation of gene networks associated with adaptive immunity was linked to the suppression of networks for tight junction, gap junctional intercellular communication, and transmembrane transporters, all of which are precursors for impaired gut integrity and performance. On a class level, DEHP exposure increased Bacteroidia and Gammaproteobacteria and decreased Verrucomicrobiae in both the male and female gastrointestinal system. Further, in males there was a relative increase in Fusobacteriia and Betaproteobacteria and a relative decrease in Saccharibacteria. Predictive algorithms revealed that the functional shift in the microbiome community, and the metabolites they produce, act to modulate intestinal adaptive immunity. This finding suggests that the gut microbiota may contribute to the adverse effects of DEHP on the host by altering metabolites sensed by both intestinal and immune Th cells. Our results suggest that the microbiome-gut-immune axis can be modified by DEHP and emphasize the value of multiomics approaches to study microbiome-host interactions following chemical perturbations.
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