TY - JOUR
T1 - TCDD influences reservoir of antibiotic resistance genes in murine gut microbiome
AU - Stedtfeld, Robert D.
AU - Stedtfeld, Tiffany M.
AU - Fader, Kelly A.
AU - Williams, Maggie R.
AU - Bhaduri, Prianca
AU - Quensen, John
AU - Zacharewski, Timothy R.
AU - Tiedje, James M.
AU - Hashsham, Syed A.
N1 - Publisher Copyright:
© FEMS 2017. All rights reserved.
PY - 2017/5/1
Y1 - 2017/5/1
N2 - Dysbiosis of the gut microbiome via antibiotics, changes in diet and infection can select for bacterial groups that more frequently harbor antimicrobial resistance genes (ARGs) and mobile genetic elements (MGEs). However, the impact of environmental toxicants on the reservoir of ARGs in the gut microbiome has received less attention. 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) is a potent aryl hydrocarbon receptor (AhR) agonist with multiple toxic health effects including immune dysfunction. The selective pressure of TCDD on the abundance of ARG and MGE-harboring gut populations was examined using C57BL/6 mice exposed to 0-30 μg/kg TCDD for 28 and 92 days with the latter having a 30-day recovery period. DNA extracted from temporally collected fecal pellets was characterized using a qPCR array with 384 assays targeting ARGs and MGEs. Fourteen genes, typically observed in Enterobacteriaceae, increased significantly within 8 days of initial dosing, persisted throughout the treatment period, and remained induced 30 days post dosing. A qPCR primer set targeting Enterobacteriaceae also showed 10- to 100-fold higher abundance in TCDD-treated groups, which was further verified using metagenomics. Results show a bloom of ARG-harboring bacterial groups in the gut due to a xenobiotic compound that is not a metal, biocide or antimicrobial.
AB - Dysbiosis of the gut microbiome via antibiotics, changes in diet and infection can select for bacterial groups that more frequently harbor antimicrobial resistance genes (ARGs) and mobile genetic elements (MGEs). However, the impact of environmental toxicants on the reservoir of ARGs in the gut microbiome has received less attention. 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) is a potent aryl hydrocarbon receptor (AhR) agonist with multiple toxic health effects including immune dysfunction. The selective pressure of TCDD on the abundance of ARG and MGE-harboring gut populations was examined using C57BL/6 mice exposed to 0-30 μg/kg TCDD for 28 and 92 days with the latter having a 30-day recovery period. DNA extracted from temporally collected fecal pellets was characterized using a qPCR array with 384 assays targeting ARGs and MGEs. Fourteen genes, typically observed in Enterobacteriaceae, increased significantly within 8 days of initial dosing, persisted throughout the treatment period, and remained induced 30 days post dosing. A qPCR primer set targeting Enterobacteriaceae also showed 10- to 100-fold higher abundance in TCDD-treated groups, which was further verified using metagenomics. Results show a bloom of ARG-harboring bacterial groups in the gut due to a xenobiotic compound that is not a metal, biocide or antimicrobial.
KW - Antibiotic resistance genes (ARGs)
KW - Dysbiosis
KW - Enterobacteriaceae
KW - Gut microbiome
KW - Immune-suppression
KW - Mobile genetic elements
KW - Persistent organic pollutant
KW - TCDD
UR - http://www.scopus.com/inward/record.url?scp=85028303080&partnerID=8YFLogxK
U2 - 10.1093/femsec/fix058
DO - 10.1093/femsec/fix058
M3 - Article
C2 - 28475713
AN - SCOPUS:85028303080
SN - 0168-6496
VL - 93
JO - FEMS Microbiology Ecology
JF - FEMS Microbiology Ecology
IS - 5
ER -