{
"METABOLOMICS WORKBENCH":{"STUDY_ID":"ST000570","ANALYSIS_ID":"AN000878","VERSION":"1","CREATED_ON":"March 13, 2017, 11:57 am"},

"PROJECT":{"PROJECT_TITLE":"Metabolome analysis of the cecal contents of GF mice and GF mice colonized with dominant gut microbes present in the ceca of neonatal and adult mice","PROJECT_SUMMARY":"The high susceptibility of neonates to infections has been assumed to be due to immaturity of the immune system, but the mechanism remains unclear. By colonizing adult germ-free mice with the cecal contents of neonatal and adult mice, we show that the neonatal microbiota is impaired in mediating colonization resistance against two major pathogens causing mortality in neonates. The lack of colonization resistance was caused by the absence of Clostridiales in the neonatal microbiota. Administration of Clostridiales, but not Bacteroidales, restored colonization resistance and abrogated intestinal pathology upon pathogen challenge. Conversely, depletion of Clostridiales abolished colonization resistance in adult mice. Furthermore, intragastric administration of Clostridiales protected neonatal mice from pathogen infection. The neonatal bacteria enhanced the ability of these protective Clostridiales to colonize the gut. These results identify the gut microbiota as a critical determinant of increased susceptibility to enteric infection during the neonatal period.","INSTITUTE":"Keio University","DEPARTMENT":"Institute for Advanced Biosciences","LAST_NAME":"Fukuda","FIRST_NAME":"Shinji","ADDRESS":"Tsuruoka, Yamagata 997-0052, Japan","EMAIL":"sfukuda@sfc.keio.ac.jp","PHONE":"+81-235-29-0528"},

"STUDY":{"STUDY_TITLE":"Metabolome analysis of the cecal contents of GF mice and GF mice colonized with dominant gut microbes present in the ceca of neonatal and adult mice","STUDY_SUMMARY":"Metabolome profiles of GF or GF mice reconstituted with Esherichia coli (EC), Bacteroides acidifaciens (Bac), or Clostridia consortium (CL) were compared.","INSTITUTE":"Keio University","DEPARTMENT":"Institute for Advanced Biosciences","LAST_NAME":"Fukuda","FIRST_NAME":"Shinji","ADDRESS":"Tsuruoka, Yamagata 997-0052, Japan","EMAIL":"sfukuda@sfc.keio.ac.jp","PHONE":"+81-235-29-0528","NUM_GROUPS":"4","TOTAL_SUBJECTS":"17"},

"SUBJECT":{"SUBJECT_TYPE":"Animal","SUBJECT_SPECIES":"Mus musculus","TAXONOMY_ID":"10090","GENOTYPE_STRAIN":"C57BL/6"},
"SUBJECT_SAMPLE_FACTORS":[
{
"Subject ID":"-",
"Sample ID":"1_B1",
"Factors":{"colonized bacteria":"Bacteroides acidifaciens"}
},
{
"Subject ID":"-",
"Sample ID":"1_B2",
"Factors":{"colonized bacteria":"Bacteroides acidifaciens"}
},
{
"Subject ID":"-",
"Sample ID":"1_B3",
"Factors":{"colonized bacteria":"Bacteroides acidifaciens"}
},
{
"Subject ID":"-",
"Sample ID":"1_B4",
"Factors":{"colonized bacteria":"Bacteroides acidifaciens"}
},
{
"Subject ID":"-",
"Sample ID":"1_B5",
"Factors":{"colonized bacteria":"Bacteroides acidifaciens"}
},
{
"Subject ID":"-",
"Sample ID":"1_CL1",
"Factors":{"colonized bacteria":"Clostridia"}
},
{
"Subject ID":"-",
"Sample ID":"1_CL2",
"Factors":{"colonized bacteria":"Clostridia"}
},
{
"Subject ID":"-",
"Sample ID":"1_CL3",
"Factors":{"colonized bacteria":"Clostridia"}
},
{
"Subject ID":"-",
"Sample ID":"1_CL4",
"Factors":{"colonized bacteria":"Clostridia"}
},
{
"Subject ID":"-",
"Sample ID":"1_CL5",
"Factors":{"colonized bacteria":"Clostridia"}
},
{
"Subject ID":"-",
"Sample ID":"2_EB1",
"Factors":{"colonized bacteria":"Esherichia coli"}
},
{
"Subject ID":"-",
"Sample ID":"2_EB2",
"Factors":{"colonized bacteria":"Esherichia coli"}
},
{
"Subject ID":"-",
"Sample ID":"2_EB3",
"Factors":{"colonized bacteria":"Esherichia coli"}
},
{
"Subject ID":"-",
"Sample ID":"5_C1",
"Factors":{"colonized bacteria":"none (GF)"}
},
{
"Subject ID":"-",
"Sample ID":"5_C2",
"Factors":{"colonized bacteria":"none (GF)"}
},
{
"Subject ID":"-",
"Sample ID":"5_C3",
"Factors":{"colonized bacteria":"none (GF)"}
},
{
"Subject ID":"-",
"Sample ID":"5_C4",
"Factors":{"colonized bacteria":"none (GF)"}
}
],
"COLLECTION":{"COLLECTION_SUMMARY":"Feces of GF or GF mice reconstituted with Esherichia coli (EC), Bacteroides acidifaciens (Bac), or Clostridia consortium (CL)","SAMPLE_TYPE":"Feces","STORAGE_CONDITIONS":"-80℃"},

"TREATMENT":{"TREATMENT_SUMMARY":"Animals Specific-pathogen-free (SPF) C57BL/6 mice were originally purchased from Jackson Laboratories. Wild-type mice on GF background were bred and maintained at the Germ-free Animal Core Facility of the University of Michigan. GF mice were maintained in flexible film isolators and were checked weekly for germ-free status by aerobic and anaerobic culture. The absence of microbiota was verified by microscopic analysis of stained cecal contents to detect unculturable contamination. All animal studies were performed according to approved protocols by the University of Michigan Committee on the Use and Care of Animals. Reconstitution of GF mice with cecal contents and defined bacteria Cecal contents from single neonatal and 7-week old SPF mice were diluted into 50 ml (per one adult mouse) or 5 ml (per one 4, 12, 16-day old mouse) of PBS, and passed through a 70 μm cell strainer to eliminate clumps and debris under sterile conditions) under an atmosphere of 5% H2, 5% CO2 and 90% N2 in an anaerobic growth chamber (Coy Manufacturing, Grass Lake, MI). Then 200 μl of the suspension was processed by intragastric gavage into each of the recipient GF mice. Bacteroides species were anaerobically grown at 37°C overnight in pre-reduced chopped-meat broth (Anaerobe systems, Morgan Hill, CA). E. coli were grown aerobically overnight in LB broth with shaking.","TREATMENT_PROTOCOL_FILENAME":"Treatment_Protocol.pdf","TREATMENT":"Biotic","TREATMENT_COMPOUND":"Suspension of diluted cecal contents","TREATMENT_ROUTE":"Intragastric gavage","TREATMENT_DOSE":"200 μl"},

"SAMPLEPREP":{"SAMPLEPREP_SUMMARY":"CE-TOFMS-based metabolome analysis(sample preparation) Fecal samples were freeze dried, and disrupted by vigorous shaking at 1,500 rpm for 10 min with four 3 mm zirconia beads by Shake Master NEO (Bio Medical Science Inc.). 10 mg (±0.5 mg) fecal samples were homogenized with 500 μl MeOH containing internal standards (20 μM each of methionine sulfone, and D-camphor-10-sulfonic acid (CSA)) and 100 mg of 0.1 mm and four of 3 mm zirconia/silica beads (BioSpec Products). After vigorous shaking (1,500 rpm for 5 min) by Shake Master NEO (Bio Medical Science Inc.), 200 μl of Milli-Q water and 500 μl of chloroform was added and then shaking in a same manner as before. After centrifugation at 4,600 × g for 15 min at 4°C, the supernatant was transferred to a 5kDa cutoff centrifugal filter tube. The filtrate was centrifugally concentrated at 40°C and reconstituted with 40 μl of Milli-Q water.","SAMPLEPREP_PROTOCOL_FILENAME":"Sample_Prep_Protocol.pdf","PROCESSING_METHOD":"Homogenized with 500 μl MeOH containing internal standards and 100 mg of 0.1 mm and four of 3 mm zirconia/silica beads","PROCESSING_STORAGE_CONDITIONS":"On ice","EXTRACTION_METHOD":"Chloroform","EXTRACT_CLEANUP":"5kDa cutoff centrifugal filter tube","SAMPLE_RESUSPENSION":"40 μl of Milli-Q water"},

"CHROMATOGRAPHY":{"CHROMATOGRAPHY_TYPE":"CE","INSTRUMENT_NAME":"Agilent CE","COLUMN_NAME":"COSMO(+), i.d.50 µm(anion), Fused-silica, i.d. 50 µm(cation)","INTERNAL_STANDARD":"20 μM each of methionine sulfone, and D-camphor-10-sulfonic acid (CSA)"},

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

"MS":{"MS_COMMENTS":"-","INSTRUMENT_NAME":"Agilent CE-TOFMS","INSTRUMENT_TYPE":"TOF","MS_TYPE":"ESI","ION_MODE":"NEGATIVE"},

"MS_METABOLITE_DATA":{
"Units":"nmol/g",

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}

}