{
"METABOLOMICS WORKBENCH":{"STUDY_ID":"ST001299","ANALYSIS_ID":"AN002163","VERSION":"1","CREATED_ON":"January 8, 2020, 9:31 am"},

"PROJECT":{"PROJECT_TITLE":"Metatranscriptomic Analysis of the Mouse Gut Microbiome Response to the Persistent Organic Pollutant 2,3,7,8-Tetrachlorodibenzofuran","PROJECT_SUMMARY":"Persistent organic pollutants (POPs) are important environmental chemicals and continued study of their mechanism of action remains a high priority. POPs, such as 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), 2,3,7,8-tetrachlorodibenzofuran (TCDF), and polychlorinated biphenyls (PCBs), are widespread environmental contaminants that are agonists for the aryl hydrocarbon receptor (AHR). Activation of the AHR modulates the gut microbiome community structure and function, host immunity, and the host metabolome. In the current study, male C57BL6/J mice were exposed, via the diet, to 5 ug/kg body weight (BW) TCDF or 24 ug/kg BW of TCDF every day for 5 days. The functional and structural changes imparted by TCDF exposure to the gut microbiome and host metabolome were explored via 16S rRNA gene amplicon sequencing, metabolomics, and bacterial metatranscriptomics. Significant changes included increases in lipopolysaccharide (LPS) biosynthesis gene expression after exposure to 24 ug/kg BW of TCDF. Increases in LPS biosynthesis were confirmed with metabolomics and LPS assays using serum obtained from TCDF-treated mice. Significant increases in gene expression within aspartate and glutamate metabolism were noted after exposure to 24 ug/kg BW of TCDF. Together, these results suggest that after exposure to 24 ug/kg BW of TCDF, the gut microbiome increases the production of LPS and glutamate to promote localized gut inflammation, potentially using glutamate as a stress response.","INSTITUTE":"The Pennsylvania State University (Penn State)","LAST_NAME":"Nichols","FIRST_NAME":"Robert","ADDRESS":"917 Old Boalsburg Road, State College, Pennsylvania, 16801, USA","EMAIL":"rgn5011@psu.edu","PHONE":"7247662694"},

"STUDY":{"STUDY_TITLE":"Metatranscriptomic Analysis of the Mouse Gut Microbiome Response to the Persistent Organic Pollutant 2,3,7,8-Tetrachlorodibenzofuran","STUDY_SUMMARY":"Persistent organic pollutants (POPs) are important environmental chemicals and continued study of their mechanism of action remains a high priority. POPs, such as 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), 2,3,7,8-tetrachlorodibenzofuran (TCDF), and polychlorinated biphenyls (PCBs), are widespread environmental contaminants that are agonists for the aryl hydrocarbon receptor (AHR). Activation of the AHR modulates the gut microbiome community structure and function, host immunity, and the host metabolome. In the current study, male C57BL6/J mice were exposed, via the diet, to 5 ug/kg body weight (BW) TCDF or 24 ug/kg BW of TCDF every day for 5 days. The functional and structural changes imparted by TCDF exposure to the gut microbiome and host metabolome were explored via 16S rRNA gene amplicon sequencing, metabolomics, and bacterial metatranscriptomics. Significant changes included increases in lipopolysaccharide (LPS) biosynthesis gene expression after exposure to 24 ug/kg BW of TCDF. Increases in LPS biosynthesis were confirmed with metabolomics and LPS assays using serum obtained from TCDF-treated mice. Significant increases in gene expression within aspartate and glutamate metabolism were noted after exposure to 24 ug/kg BW of TCDF. Together, these results suggest that after exposure to 24 ug/kg BW of TCDF, the gut microbiome increases the production of LPS and glutamate to promote localized gut inflammation, potentially using glutamate as a stress response.","INSTITUTE":"The Pennsylvania State University (Penn State)","LAST_NAME":"Nichols","FIRST_NAME":"Robert","ADDRESS":"917 Old Boalsburg Road, State College, Pennsylvania, 16801, USA","EMAIL":"rgn5011@psu.edu","PHONE":"7247662694"},

"SUBJECT":{"SUBJECT_TYPE":"Mammal","SUBJECT_SPECIES":"Mus musculus","TAXONOMY_ID":"10090"},
"SUBJECT_SAMPLE_FACTORS":[
{
"Subject ID":"-",
"Sample ID":"C1",
"Factors":{"Treatment":"Control"},
"Additional sample data":{"RAW_FILE_NAME":"BN181022_06.raw"}
},
{
"Subject ID":"-",
"Sample ID":"C2",
"Factors":{"Treatment":"Control"},
"Additional sample data":{"RAW_FILE_NAME":"SH181022_19.raw"}
},
{
"Subject ID":"-",
"Sample ID":"C3",
"Factors":{"Treatment":"Control"},
"Additional sample data":{"RAW_FILE_NAME":"SH181022_22.raw"}
},
{
"Subject ID":"-",
"Sample ID":"C4",
"Factors":{"Treatment":"Control"},
"Additional sample data":{"RAW_FILE_NAME":"BN181022_11.raw"}
},
{
"Subject ID":"-",
"Sample ID":"C5",
"Factors":{"Treatment":"Control"},
"Additional sample data":{"RAW_FILE_NAME":"SH181022_17.raw"}
},
{
"Subject ID":"-",
"Sample ID":"C6",
"Factors":{"Treatment":"Control"},
"Additional sample data":{"RAW_FILE_NAME":"BN181022_13.raw"}
},
{
"Subject ID":"-",
"Sample ID":"L1",
"Factors":{"Treatment":"Low Dose TCDF"},
"Additional sample data":{"RAW_FILE_NAME":"BN181022_04.raw"}
},
{
"Subject ID":"-",
"Sample ID":"L2",
"Factors":{"Treatment":"Low Dose TCDF"},
"Additional sample data":{"RAW_FILE_NAME":"SH181022_20.raw"}
},
{
"Subject ID":"-",
"Sample ID":"L3",
"Factors":{"Treatment":"Low Dose TCDF"},
"Additional sample data":{"RAW_FILE_NAME":"BN181022_12.raw"}
},
{
"Subject ID":"-",
"Sample ID":"L4",
"Factors":{"Treatment":"Low Dose TCDF"},
"Additional sample data":{"RAW_FILE_NAME":"BN181022_09.raw"}
},
{
"Subject ID":"-",
"Sample ID":"L5",
"Factors":{"Treatment":"Low Dose TCDF"},
"Additional sample data":{"RAW_FILE_NAME":"BN181022_10.raw"}
},
{
"Subject ID":"-",
"Sample ID":"L6",
"Factors":{"Treatment":"Low Dose TCDF"},
"Additional sample data":{"RAW_FILE_NAME":"BN181022_16.raw"}
},
{
"Subject ID":"-",
"Sample ID":"H1",
"Factors":{"Treatment":"High Dose TCDF"},
"Additional sample data":{"RAW_FILE_NAME":"SH181022_18.raw"}
},
{
"Subject ID":"-",
"Sample ID":"H2",
"Factors":{"Treatment":"High Dose TCDF"},
"Additional sample data":{"RAW_FILE_NAME":"BN181022_15.raw"}
},
{
"Subject ID":"-",
"Sample ID":"H3",
"Factors":{"Treatment":"High Dose TCDF"},
"Additional sample data":{"RAW_FILE_NAME":"BN181022_08.raw"}
},
{
"Subject ID":"-",
"Sample ID":"H4",
"Factors":{"Treatment":"High Dose TCDF"},
"Additional sample data":{"RAW_FILE_NAME":"SH181022_21.raw"}
},
{
"Subject ID":"-",
"Sample ID":"H5",
"Factors":{"Treatment":"High Dose TCDF"},
"Additional sample data":{"RAW_FILE_NAME":"BN181022_14.raw"}
},
{
"Subject ID":"-",
"Sample ID":"H6",
"Factors":{"Treatment":"High Dose TCDF"},
"Additional sample data":{"RAW_FILE_NAME":"BN181022_07.raw"}
}
],
"COLLECTION":{"COLLECTION_SUMMARY":"Cecal contents were extracted and then sub sampled for analysis. 100mgs of cecal contents were then used for extraction.","SAMPLE_TYPE":"Cecum"},

"TREATMENT":{"TREATMENT_SUMMARY":"Mice were treated with either 5 ug/kg of TCDF or 24 ug/kg of TCDF or untreated dough pills"},

"SAMPLEPREP":{"SAMPLEPREP_SUMMARY":"See attached Sample prep doc (GC_Sample_Prep.doc)"},

"CHROMATOGRAPHY":{"CHROMATOGRAPHY_TYPE":"Reversed phase","INSTRUMENT_NAME":"Thermo Dionex Ultimate 3000","COLUMN_NAME":"Hydro-RP C18 column"},

"ANALYSIS":{"ANALYSIS_TYPE":"MS"},

"MS":{"INSTRUMENT_NAME":"Thermo Q Exactive Plus Orbitrap","INSTRUMENT_TYPE":"Orbitrap","MS_TYPE":"ESI","ION_MODE":"POSITIVE","MS_COMMENTS":"none"},

"MS_METABOLITE_DATA":{
"Units":"ppm",

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}

}