#METABOLOMICS WORKBENCH bastiseelbinder_20230323_053437 DATATRACK_ID:3813 STUDY_ID:ST002523 ANALYSIS_ID:AN004157 PROJECT_ID:PR001625
VERSION             	1
CREATED_ON             	March 23, 2023, 7:43 am
#PROJECT
PR:PROJECT_TITLE                 	Metabolomics of human urine
PR:PROJECT_TYPE                  	MS quantitative analysis
PR:PROJECT_SUMMARY               	Metabolomics of human urine to support the findings in Candida expansion in the
PR:PROJECT_SUMMARY               	gut of lung cancer patients associates with an ecological signature that
PR:PROJECT_SUMMARY               	supports growth under dysbiotic conditions
PR:INSTITUTE                     	Leibniz Institute for Natural Product Research and Infection Biology Hans Knöll
PR:INSTITUTE                     	Institute (Leibniz-HKI)
PR:DEPARTMENT                    	Microbiome Dynamics
PR:LAST_NAME                     	Seelbinder
PR:FIRST_NAME                    	Bastian
PR:ADDRESS                       	Beutenbergstraße 11a, Jena, Thuringia, 07745, Germany
PR:EMAIL                         	bastian.seelbinder@leibniz-hki.de
PR:PHONE                         	+4936415321360
#STUDY
ST:STUDY_TITLE                   	Candida expansion in the human gut is associated with an ecological signature
ST:STUDY_TITLE                   	that supports growth under dysbiotic conditions
ST:STUDY_SUMMARY                 	The overgrowth of Candida species in the human gut is considered a prerequisite
ST:STUDY_SUMMARY                 	for invasive candidiasis. However, our understanding of how gut bacteria promote
ST:STUDY_SUMMARY                 	or restrict overgrowth of Candida species in the human gut is still limited. By
ST:STUDY_SUMMARY                 	integrating mycobiome and shotgun metagenomics data from stool of 75 patients at
ST:STUDY_SUMMARY                 	risk but with no systemic candidiasis, we revealed that bacterial communities
ST:STUDY_SUMMARY                 	from high Candida samples had greater metabolic potential whereas communities
ST:STUDY_SUMMARY                 	from low Candida had greater functional redundancy. In addition, we developed
ST:STUDY_SUMMARY                 	machine learning models that used only bacterial taxa or functional relative
ST:STUDY_SUMMARY                 	abundances to predict the levels of Candida genus and species in an external
ST:STUDY_SUMMARY                 	validation cohort with an area under the curve of 78.6-81.1%. Last, we proposed
ST:STUDY_SUMMARY                 	an intriguing mechanism for Candida species overgrowth based on a decrease in
ST:STUDY_SUMMARY                 	short-chain fatty acid producing-bacteria resulting in increased oxygen levels.
ST:STUDY_SUMMARY                 	These conditions create a metabolic niche for Candida species to use lactate as
ST:STUDY_SUMMARY                 	a carbon source and overtake their fungal competitors in the human gut.
ST:INSTITUTE                     	Leibniz Institute for Natural Product Research and Infection Biology Hans Knöll
ST:INSTITUTE                     	Institute (Leibniz-HKI)
ST:DEPARTMENT                    	Microbiome Dynamics
ST:LAST_NAME                     	Bastian
ST:FIRST_NAME                    	Seelbinder
ST:ADDRESS                       	Beutenbergstraße 11a, Jena, Thuringia, 07745, Germany
ST:EMAIL                         	bastian.seelbinder@leibniz-hki.de
ST:PHONE                         	+4936415321360
#SUBJECT
SU:SUBJECT_TYPE                  	Human
SU:SUBJECT_SPECIES               	Homo sapiens
SU:TAXONOMY_ID                   	9606
SU:AGE_OR_AGE_RANGE              	68 (63, 73)
SU:WEIGHT_OR_WEIGHT_RANGE        	77 (62, 87)
SU:HEIGHT_OR_HEIGHT_RANGE        	170 (160, 176)
SU:GENDER                        	Male and female
SU:HUMAN_ETHNICITY               	White
SU:HUMAN_MEDICATIONS             	anti-PD-1 immune checkpoint inhibitors (nivolumab or pembrolizumab)
SU:HUMAN_INCLUSION_CRITERIA      	consecutive advanced cancer patients
#FACTORS
#SUBJECT_SAMPLE_FACTORS:         	SUBJECT(optional)[tab]SAMPLE[tab]FACTORS(NAME:VALUE pairs separated by |)[tab]Raw file names and additional sample data
SUBJECT_SAMPLE_FACTORS           	-	MK115	Candida:Low | Gender:Female | Immunotherapy:Nivolumab	RAW_FILE_NAME=220922-LC1-PAN-1-030-SA008756.mzML
SUBJECT_SAMPLE_FACTORS           	-	MK175	Candida:High | Gender:Female | Immunotherapy:Pembrolizumab	RAW_FILE_NAME=220922-LC1-PAN-1-036-SA008762.mzML
SUBJECT_SAMPLE_FACTORS           	-	MK209	Candida:High | Gender:Male | Immunotherapy:Nivolumab	RAW_FILE_NAME=220922-LC1-PAN-1-027-SA008757.mzML
SUBJECT_SAMPLE_FACTORS           	-	MK227	Candida:Low | Gender:Female | Immunotherapy:Nivolumab	RAW_FILE_NAME=220922-LC1-PAN-1-039-SA008759.mzML
SUBJECT_SAMPLE_FACTORS           	-	MK251	Candida:Low | Gender:Male | Immunotherapy:Nivolumab	RAW_FILE_NAME=220922-LC1-PAN-1-024-SA008768.mzML
SUBJECT_SAMPLE_FACTORS           	-	MK279	Candida:Low | Gender:Male | Immunotherapy:Pembrolizumab	RAW_FILE_NAME=220922-LC1-PAN-1-032-SA008765.mzML
SUBJECT_SAMPLE_FACTORS           	-	MK287	Candida:Low | Gender:Female | Immunotherapy:Pembrolizumab	RAW_FILE_NAME=220922-LC1-PAN-1-019-SA008754.mzML
SUBJECT_SAMPLE_FACTORS           	-	MK300	Candida:High | Gender:Male | Immunotherapy:Pembrolizumab	RAW_FILE_NAME=220922-LC1-PAN-1-031-SA008764.mzML
SUBJECT_SAMPLE_FACTORS           	-	MK304	Candida:High | Gender:Male | Immunotherapy:Nivolumab	RAW_FILE_NAME=220922-LC1-PAN-1-026-SA008763.mzML
SUBJECT_SAMPLE_FACTORS           	-	MK311	Candida:High | Gender:Male | Immunotherapy:Nivolumab	RAW_FILE_NAME=220922-LC1-PAN-1-022-SA008767.mzML
SUBJECT_SAMPLE_FACTORS           	-	MK324	Candida:High | Gender:Male | Immunotherapy:Pembrolizumab	RAW_FILE_NAME=220922-LC1-PAN-1-038-SA008751.mzML
SUBJECT_SAMPLE_FACTORS           	-	MK329	Candida:High | Gender:Male | Immunotherapy:Nivolumab	RAW_FILE_NAME=220922-LC1-PAN-1-028-SA008758.mzML
SUBJECT_SAMPLE_FACTORS           	-	MT196	Candida:High | Gender:Male | Immunotherapy:Pembrolizumab	RAW_FILE_NAME=220922-LC1-PAN-1-025-SA008753.mzML
SUBJECT_SAMPLE_FACTORS           	-	MT238	Candida:Low | Gender:Male | Immunotherapy:Nivolumab	RAW_FILE_NAME=220922-LC1-PAN-1-034-SA008749.mzML
SUBJECT_SAMPLE_FACTORS           	-	MT239	Candida:High | Gender:Female | Immunotherapy:Pembrolizumab	RAW_FILE_NAME=220922-LC1-PAN-1-040-SA008755.mzML
SUBJECT_SAMPLE_FACTORS           	-	MT241	Candida:High | Gender:Male | Immunotherapy:Pembrolizumab	RAW_FILE_NAME=220922-LC1-PAN-1-037-SA008752.mzML
SUBJECT_SAMPLE_FACTORS           	-	MT242	Candida:Low | Gender:Female | Immunotherapy:Nivolumab	RAW_FILE_NAME=220922-LC1-PAN-1-018-SA008750.mzML
SUBJECT_SAMPLE_FACTORS           	-	MT245	Candida:Low | Gender:Male | Immunotherapy:Nivolumab	RAW_FILE_NAME=220922-LC1-PAN-1-033-SA008760.mzML
SUBJECT_SAMPLE_FACTORS           	-	MT252	Candida:Low | Gender:Male | Immunotherapy:Nivolumab	RAW_FILE_NAME=220922-LC1-PAN-1-020-SA008761.mzML
#COLLECTION
CO:COLLECTION_SUMMARY            	Human urine samples were collected by from lung cancer patients and frozen at
CO:COLLECTION_SUMMARY            	-80 °C. Samples were shipped to MS-OMICS for metabolomic analysis.
CO:SAMPLE_TYPE                   	Urine
CO:STORAGE_CONDITIONS            	-80℃
#TREATMENT
TR:TREATMENT_SUMMARY             	To unfreeze samples at MS-OMICS, samples were assigned to their SpinX filters
TR:TREATMENT_SUMMARY             	and centrifugated at 15,000 RPM for 5 minutes at 4 °C. Urine samples were then
TR:TREATMENT_SUMMARY             	diluted 11 times in mobile phase eluent A and fortified with stable isotope
TR:TREATMENT_SUMMARY             	labelled standards before analysis.
TR:TREATMENT_COMPOUND            	mobile phase eluent A
#SAMPLEPREP
SP:SAMPLEPREP_SUMMARY            	Urine samples were then diluted 11 times in mobile phase eluent A and fortified
SP:SAMPLEPREP_SUMMARY            	with stable isotope labelled standards before analysis.
#CHROMATOGRAPHY
CH:CHROMATOGRAPHY_SUMMARY        	The samples were analysed with our semi-polar metabolites method, which is a
CH:CHROMATOGRAPHY_SUMMARY        	slightly modified version of the protocol described by Catalin et al. (UPLC/MS
CH:CHROMATOGRAPHY_SUMMARY        	Monitoring of Water-Soluble Vitamin Bs in Cell Culture Media in Minutes, Water
CH:CHROMATOGRAPHY_SUMMARY        	Application note 2011, 720004042en). The analysis was carried out in a
CH:CHROMATOGRAPHY_SUMMARY        	randomised order using a UPLC system (Vanquish, Thermo Fisher Scientific)
CH:CHROMATOGRAPHY_SUMMARY        	coupled with a high-resolution quadrupole-orbitrap mass spectrometer Orbitrap
CH:CHROMATOGRAPHY_SUMMARY        	Exploris 240 MS, Thermo Fisher Scientific.
CH:CHROMATOGRAPHY_TYPE           	Reversed phase
CH:INSTRUMENT_NAME               	Thermo Vanquish
CH:COLUMN_NAME                   	Waters ACQUITY UPLC HSS T3 (150 x 2.1mm,1.8um)
CH:SOLVENT_A                     	10 mM ammonium formate, 0.1% formic acid in water (pH 3.1)
CH:SOLVENT_B                     	10 mM ammonium formate, 0.1% formic acid in methanol
CH:FLOW_GRADIENT                 	300 μL/min: 0-2 min: 0% B, 2-12 min: 35% B, 12-13 min: 90% B, 13-14 min: 90% B,
CH:FLOW_GRADIENT                 	14-15 min: 0% B
CH:FLOW_RATE                     	300 μL/min
CH:COLUMN_TEMPERATURE            	30
#ANALYSIS
AN:ANALYSIS_TYPE                 	MS
#MS
MS:INSTRUMENT_NAME               	Thermo Orbitrap Exploris 240
MS:INSTRUMENT_TYPE               	QTRAP
MS:MS_TYPE                       	ESI
MS:ION_MODE                      	POSITIVE
MS:MS_COMMENTS                   	The ionization was achieved with an electrospray ionization interface operated
MS:MS_COMMENTS                   	in positive and negative ionization mode under polarity switching. Data were
MS:MS_COMMENTS                   	processed using Compound Discoverer 3.3 (Thermo Fisher Scientific) and Skyline
MS:MS_COMMENTS                   	21.2.
MS:MS_RESULTS_FILE               	ST002523_AN004157_Results.txt	UNITS:Peak area	Has m/z:Neutral masses	Has RT:Yes	RT units:Minutes
#END