Mother-infant gut microbiome strain transmission cohort
Longitudinal cohort study of 212 faecal metagenome samples from infants and family members in Germany, the Netherlands, and Luxembourg, examining maternal strain transmission and colonisation of the infant gut microbiome. machine-written summary
212 samples · 633 runs · DE, LU, NL · Infant / toddler · 2018 · 4.42 Gbp / sample
Checked this project's papers and archive records yourself? Mark it human-verified.
what each source gave
| ✓ Sequence archive | 424 sample values (collection date, country) |
| ○ Abstract / description | read; no usable statement |
| ○ Full text | read; no usable statement or table · PMC13288982, PMC5880245 |
| ○ Supplementary tables | files read; no table could be matched to the samples |
| – External resources | not covered by the external resources we ingest |
| – User contribution | nothing uploaded yet · share metadata |
| – Human verified | not yet checked by a person · I checked this project — verify it |
longitudinal — not resolvedfamilies — not resolvedfather–child — not resolvedmother–infant — not resolvedsiblings — not resolvedtwins — not resolved
Schedule stated by the source: “Paper states cohort (incl. this subset) was sampled at multiple time points; exact per-subject schedule for this German/Dutch subset not given.”.
10 German/Dutch families (fathers, mothers, siblings, twins); 212 samples; per-sample family/role not in archive (Suppl. Table S2 counts only).
Genera, mean relative abundance over 186 profiled gut samples of this project (Sandpiper SingleM profiles, GTDB R232; low-depth and non-metagenome profiles left out).
| field | samples | coverage | R1 | R2 | R3 | R4 |
|---|---|---|---|---|---|---|
| age_category | 0 | 0% | ||||
| country | 212 | 100% | 212 | |||
| health_condition | 0 | 0% | ||||
| subject_id | 0 | 0% | ||||
| collection_date | 212 | 100% | 212 |
- Selective maternal seeding and environment shape the human gut microbiome. PMID 29496731 PMC5880245 curated
- Metagenomic polymorphic toxin effector and immunity profiling predicts microbiome development and disease-related dysbiosis. PMID 42171373 PMC13288982 curated
Archive description
Vertical transmission of bacteria from mother to infant at birth is assumed to initiate a life-long host-microbe symbiosis. Maternal bacteria are expected to seed the infant intestine and thus play an important role in early development. However, only tracking of strictly defined microbial strains can clarify where the intestinal bacteria come from, how long the initial colonisers persist and whether colonisation by other strains from the environment can replace existing ones. Using rare single nucleotide variants in faecal metagenomes of infants and their family members, we show strong evidence of selective and persistent transmission of maternal strain populations to the vaginally born infant, and their occasional replacement by strains from the environment, including those from family members, in later childhood. Only strains from the classes Actinobacteria and Bacteroidia, which are essential components of the infant microbiome, are transmitted from the mother and persist for at least one year. In contrast, maternal strains of Clostridia, a dominant class in the mother’s gut microbiome, are not observed in the infant. Instead, Clostridia strains are recruited from the environment early on, and fail to colonise persistently until after the first year. Caesarean-born infants showed a striking lack of maternal transmission at birth. For all children analysed, strain influx from the family environment was observed, peaking after the first year. Furthermore, even in adulthood strain sharing between family members, including spouses and siblings, is more common than between unrelated individuals. This suggests that re-colonisation occurs in adulthood. When studying families, fathers appear to be more frequently donors of novel strains to other family members than receivers. Taken together, after selective maternal seeding of the infant gut, species from the environment are recruited, with a rare but continuing strain influx over time.
How this project entered the registry
Classified as human gut / stool shotgun DNA metagenome of infant / toddler and adult and child by deterministic_prior with confidence 0.90. Assay shotgun_dna.
- host external_curation.infant_catalog · “infant triage verdict include”
- body site study.title · “shape the human gut microbiome”
- body site study.description · “seed the infant intestine and thus play”
- life stage external_curation.infant_catalog · “infant triage verdict include (0-3 y scope)”
- life stage study.description · “from mother to infant at birth is”
- life stage study.title · “Selective maternal seeding and environment”
- life stage study.description · “life-long host-microbe symbiosis. Maternal bacteria are expected”
- life stage study.description · “members, in later childhood . Only strains”
Evidence examples (one per field × route)
| sample | field | value | route | conf. | source | quote |
|---|---|---|---|---|---|---|
| SAMEA104445433 | collection_date | 2014-03-27 | R1 | 0.85 | biosample.attribute:collection_date | collection_date: 2014-03-27 |
| SAMEA104445433 | country | NL | R1 | 0.90 | biosample_attr | Netherlands |
Sequencing
633 runs over 212 samples · mean 1.50 Gbp per run (median 1.27 Gbp, total 952.11 Gbp; 633 runs with a base count) · layout PAIRED 633 · platform ILLUMINA 633 · models Illumina HiSeq 2000 (633) · 74% of runs with a Sandpiper profile · first public 2018-02-12
Authors (13)
Korpela K first · Costea P · Coelho LP · Kandels-Lewis S · Willemsen G · Boomsma DI · Segata N · Bork P last · Schroer HW first · Beghini F · Raygoza Garay JA · Christakis NA · Bosch DE last
Help complete this project
3 of the 4 core fields are below 50% coverage: age_category, health_condition, subject_id. Share metadata
Downloads
PRJEB24041.csv.gz (6.1 KB) · parquet (77.9 KB) — all 212 samples, every field with route and confidence · PRJEB24041_determinations.csv.gz (2.3 KB) — 424 evidence rows