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PRJEB28687 ERP110930

Gut microbiome in Hmong/Karen immigrants and US residents

U.S. immigration westernizes the human gut microbiome

Cross-sectional study of 55 samples from individuals in the USA, part of a larger project examining how US immigration affects gut microbiome diversity in Hmong and Karen populations compared to European Americans. machine-written summary

55 samples · 55 runs · US · Adult · 2018 · 5.60 Gbp / sample

Sources
✓Sequence archive 297○Abstract / description○Full text○Supplementary tables–External resources–User contribution–Human verified

Checked this project's papers and archive records yourself? Mark it human-verified.

what each source gave
✓ Sequence archive297 sample values (collection date, country, latitude, location region, longitude, subject id, timepoint)
○ Abstract / descriptionread; no usable statement
○ Full textread; no usable statement or table · PMC10165778, PMC10201371, PMC10913632, PMC6498444
○ Supplementary tablesfiles read; no table could be matched to the samples
– External resourcesnot covered by the external resources we ingest
– User contributionnothing uploaded yet · share metadata
– Human verifiednot yet checked by a person · I checked this project — verify it
Interventions

intervention — arms not resolved

design observational_with_procedure

Samples at a glance
1 sampling locations · 1 country
Age
adult55
Country
US55
Body site
primary55
Sequencing depth per sample · this project all projects
all projects, 0–0.03 Gbp: 25,080 samples (4 %)all projects, 0.03–0.1 Gbp: 17,066 samples (3 %)all projects, 0.1–0.3 Gbp: 29,179 samples (5 %)all projects, 0.3–1 Gbp: 47,044 samples (8 %)all projects, 1–3 Gbp: 124,983 samples (22 %)all projects, 3–10 Gbp: 253,728 samples (44 %)this project, 3–10 Gbp: 55 samplesall projects, 10–30 Gbp: 72,533 samples (13 %)all projects, 30–100 Gbp: 3,024 samples (1 %)all projects, 100–300 Gbp: 106 samples (0 %)all projects, ≥ 300 Gbp: 9 samples (0 %)project median 5.60 Gbp per sample0130Gbp
Sampling design and relatedness

longitudinal

5 of 6 people sampled more than once (10 samples; median 2, up to 2 per person) · follow-up median 5 mo (max 5 mo) · median interval between samples 5 mo (time from timepoint labels). Schedule stated by the source: “stool sampled before and after immigration (no fixed interval stated)” (time origin: other).

002002: day 0002: day 152003003: day 0003: day 152022022: day 0022: day 152024024: day 0024: day 152031031: day 0031: day 1520 d38 d3 mo4 mo5 mo

Each row is one person (5 shown); dots are samples at days since that person's first sample.

How longitudinal and relatedness information is derived

Community composition
Prevotella 18.0%Faecalibacterium 7.4%Roseburia 6.8%Bacteroides 4.9%Phocaeicola 4.6%Ruminococcoides 3.3%Blautia_A 3.3%Lachnospira 2.7%Alistipes 1.8%Mediterraneibacter 1.8%Bifidobacterium 1.3%Acetatifactor 1.3%not assigned to a genus 6.4%other genera 36.3%

Genera, mean relative abundance over 47 profiled gut samples of this project (Sandpiper SingleM profiles, GTDB R232; low-depth and non-metagenome profiles left out).

Field coverage
fieldsamplescoverageR1R2R3R4
age_category55 100%
country55 100%55
health_condition0 0%
subject_id11 20%11
collection_date55 100%55
detailed_location55 100%
latitude55 100%55
location_region55 100%55
longitude55 100%55
timepoint_label11 20%11
Papers (4)
  • US Immigration Westernizes the Human Gut Microbiome. 2018 PMID 30388453 PMC6498444 own_data
  • Reconstructing the landscape of gut microbial species across 29,000 diverse individuals. 2023 PMID 37070603 PMC10201371 own_data
  • Gut microbiome transitions across generations in different ethnicities in an urban setting-the HELIUS study. 2023 PMID 37158898 PMC10165778 own_data
  • Proportion-based normalizations outperform compositional data transformations in machine learning applications 2024 PMC10913632 unsure
Details
Archive description

Many United States immigrant populations develop metabolic diseases post-immigration, but the causes are not well understood. Although the microbiome plays a role in metabolic disease, there have been no studies measuring the effects of U.S. immigration on the gut microbiome. We collected stool, dietary recalls, and anthropometrics from 514 Hmong and Karen individuals living in Thailand and the U.S., including first- and second-generation immigrants and 19 Karen individuals sampled before and after immigration, as well as from 36 U.S.-born European American individuals. Using 16S and deep shotgun metagenomic DNA sequencing, we found that migration from a non-Western country to the U.S. is associated with immediate loss of gut microbiome diversity and function, in which U.S.-associated strains and functions displace native strains and functions. These effects increase with duration of U.S. residence, and are compounded by obesity and across generations.

How this project entered the registry

Classified as human gut / stool shotgun DNA metagenome of adult by deterministic_prior with confidence 0.90. Assay shotgun_dna.

  • host external_curation.infant_catalog · “infant triage reason_code age_adult_only”
  • body site study.title · “westernizes the human gut microbiome”
  • body site study.description · “immigration on the gut microbiome. We collected”
  • life stage external_curation.infant_catalog · “infant triage reason_code age_adult_only”
Evidence examples (one per field × route)
samplefieldvaluerouteconf.sourcequote
SAMEA4973145collection_date2016R10.90biosample.attribute:collection_date2016
SAMEA4973145countryUSR10.90sample.attr.geographic_location_country_and_or_seaUSA
SAMEA4973145latitude44.9778R10.90biosample.attribute:geographic_location_latitude+geographic_location_longitude44.9778� N 93.2650� W
SAMEA4973145location_regionMinnesotaR10.60biosample.attribute:geographic_location_latitude+geographic_location_longitude44.9778� N 93.2650� W
SAMEA4973145longitude-93.2650R10.90biosample.attribute:geographic_location_latitude+geographic_location_longitude44.9778� N 93.2650� W
SAMEA4973174subject_id002R10.70sample.name_rule:sample_aliaswgs.L_002_M1
SAMEA4973174timepoint_labelM1R10.70sample.name_rule:sample_aliaswgs.L_002_M1
Sequencing

55 runs over 55 samples · mean 5.61 Gbp per run (median 5.60 Gbp, total 308.33 Gbp; 55 runs with a base count) · layout PAIRED 55 · platform ILLUMINA 55 · models Illumina HiSeq 2500 (55) · 85% of runs with a Sandpiper profile · first public 2018-10-31

Authors (53)

Vangay P first · Johnson AJ · Ward TL · Al-Ghalith GA · Shields-Cutler RR · Hillmann BM · Lucas SK · Beura LK · Thompson EA · Till LM · Batres R · Paw B · Pergament SL · Saenyakul P · Xiong M · Kim AD · Kim G · Masopust D · Martens EC · Angkurawaranon C · McGready R · Kashyap PC · Culhane-Pera KA · Knights D last · Tarracchini C first · Fontana F · Mancabelli L · Lugli GA · Alessandri G · Turroni F · Ventura M · Milani C last · Segota I first · Watrous JD · Kantz ED · Nallamshetty S · Tiwari S · Cheng S · Jain M · Long T last · van der Vossen EWJ first · Davids M · Bresser LRF · Galenkamp H · van den Born BH · Zwinderman AH · Levin E · Nieuwdorp M · de Goffau MC last · van Sinderen D · Yerke A first · Fry Brumit D · Fodor A last

Help complete this project

2 of the 4 core fields are below 50% coverage: health_condition, subject_id. Share metadata

Downloads

PRJEB28687.csv.gz (2.2 KB) · parquet (71.6 KB) — all 55 samples, every field with route and confidence · PRJEB28687_determinations.csv.gz (2.3 KB) — 297 evidence rows

Samples (55 · every field this project has values for · hover a cell for its source)
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