NICU infant gut microbiome, Pittsburgh, longitudinal cohort
158 fecal samples from neonates/infants hospitalized in a Pittsburgh ICU, including preterm NICU and NEC cases, analyzed for strain persistence and sharing in a longitudinal cohort design. machine-written summary
158 samples · 158 runs · US · Infant / toddler · 2016 · 2.99 Gbp / sample · cohort Brown 2018 USA
Checked this project's papers and archive records yourself? Mark it human-verified.
what each source gave
| ✓ Sequence archive | 175 sample values (collection date, country, subject id) |
| ○ Abstract / description | read; no usable statement |
| ✓ Full text | 316 sample values (location locality, location site) · PMC10175488, PMC10230729, PMC10904392, PMC11170968, PMC11322291, PMC12677589, PMC5148203, PMC5703836, PMC5893878, PMC6905865, PMC9437082, PMC9445129, PMC9720133 |
| ✓ Supplementary tables | 1,894 sample values (age, antibiotic exposure, birth weight grams, delivery mode, diet, feeding mode, gestational age weeks, health condition) |
| ✓ External resources | 12 sample values (age, sex) · from MicrobiomeDB (VEuPathDB) |
| – User contribution | nothing uploaded yet |
| – Human verified | not yet checked by a person · I checked this project — verify it |
longitudinalsiblings — not resolved
13 of 23 people sampled more than once (147 samples; median 11, up to 22 per person) · follow-up median 24 d (max 48 d) · median interval between samples 1 d (time from age at collection). Schedule stated by the source: “Fecal samples collected at multiple days (e.g. 0,4,7,10,13,16,19,22) per infant during NICU stay” (time origin: birth).
Each row is one person (13 shown); dots are samples at days since that person's first sample.
NICU preterm infants; description states non-identical siblings shared strains; sibling pairs not identified in archive metadata.
Genera, mean relative abundance over 138 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 | 158 | 100% | ||||
| country | 158 | 100% | 158 | |||
| health_condition | 141 | 89% | 141 | |||
| subject_id | 157 | 99% | 6 | 151 | ||
| detailed_location | 158 | 100% | ||||
| location_locality | 158 | 100% | 158 | |||
| location_site | 158 | 100% | 158 | |||
| sex | 157 | 99% | 157 | |||
| age_at_collection_days | 147 | 93% | 147 | |||
| diet | 147 | 93% | 147 | |||
| antibiotic_exposure | 146 | 92% | 146 | |||
| birth_weight_grams | 141 | 89% | 141 | |||
| delivery_mode | 141 | 89% | 141 | |||
| feeding_mode | 141 | 89% | 141 | |||
| gestational_age_weeks | 141 | 89% | 141 | |||
| health_condition_detail | 141 | 89% | 141 | |||
| nec_status | 141 | 89% | 141 | |||
| preterm_status | 141 | 89% | 141 | |||
| timepoint_label | 30 | 19% | 30 | |||
| collection_date | 11 | 7% | 11 |
- Evidence for persistent and shared bacterial strains against a background of largely unique gut colonization in hospitalized premature infants. PMID 27258951 PMC5148203 curated
- Strain-resolved analysis of hospital rooms and infants reveals overlap between the human and room microbiome. PMID 29180750 PMC5703836 curated
- Hospitalized Premature Infants Are Colonized by Related Bacterial Strains with Distinct Proteomic Profiles. PMID 29636439 PMC5893878 curated
- Necrotizing enterocolitis is preceded by increased gut bacterial replication, Klebsiella, and fimbriae-encoding bacteria. PMID 31844663 PMC6905865 curated
- A compendium of 32,277 metagenome-assembled genomes and over 80 million genes from the early-life human gut microbiome. PMID 36050292 PMC9437082 curated
8 more
- Metabolic model of necrotizing enterocolitis in the premature newborn gut resulting from enteric dysbiosis. PMID 36081629 PMC9445129
- Antibiotic resistance and host immune system-induced metal bactericidal control are key factors for microbial persistence in the developing human preterm infant gut microbiome. PMID 36478853 PMC9720133
- Comprehensive insights from composition to functional microbe-based biodiversity of the infant human gut microbiota. PMID 37169786 PMC10175488
- Metagenome-mining indicates an association between bacteriocin presence and strain diversity in the infant gut. PMID 37259063 PMC10230729
- A metagenomic catalog of the early-life human gut virome. PMID 38424077 PMC10904392
- Infant age inversely correlates with gut carriage of resistance genes, reflecting modifications in microbial carbohydrate metabolism during early life. PMID 38882494 PMC11170968
- Insights into the ecology of the infant gut plasmidome. PMID 39138199 PMC11322291
- The Gut Resistome Atlas in Preterm Infants Enables Prediction of Necrotizing Enterocolitis Onset. PMID 41025564 PMC12677589
Archive description
Bacteria that persist in hospitals can contribute to the establishment of the microbiome in newborns and the spread of hospital-acquired diseases. Yet we know little about microbial communities in hospitals, or about the extent to which persistent vs. recently immigrated bacterial strains establish in the gastrointestinal tracts of hospitalized individuals.</p><p>In combination with BioProject PRJNA273761 (10 infants / 55 samples) we analyzed strain-resolved genomes obtained from a total of 202 samples collected over a three-year period from 21 infants hospitalized in the same intensive care unit.</p><p>Strains were rarely shared, consistent with prior analysis of a subset of these data. Enterococcus faecalis and Staphylococcus epidermidis, common gut colonists, exhibit diversity comparable to that of NCBI reference strains, suggesting no recent common ancestor for all populations in this hospital setting. Thus, we infer multiple introduction events for these species. Despite the rarity of shared strains, strains of five species exhibiting a degree of sequence variation consistent with in situ diversification were identified in different infants hospitalized three years apart. Three were also detected in multiple infants in the same year, suggesting that these strains are unusually widely dispersed and persistent in the hospital environment. Persistent strains were not significantly different from non-persistent strains with regards to pathogenicity potential including antibiotic resistance. Notably, non-identical siblings had multiple abundant strains in common, even 30 days after birth and antibiotic administration, suggesting overlapping strain sources and/or genetic selection. Our approach can be used in order to study microbial dynamics in hospitals and provides an important step towards directing health-promoting colonization in hospitalized individuals.
How this project entered the registry
Classified as human gut / stool / skin shotgun DNA metagenome of infant / toddler and neonate by deterministic_prior with confidence 0.90. Assay shotgun_dna.
- host external_curation.infant_catalog · “infant triage verdict include”
- body site study.title · “11 human infant fecal samples hospitalized in”
- body site study.description · “establish in the gastrointestinal tracts of hospitalized”
- body site study.description · “faecalis and Staphylococcus epidermidis , common gut”
- life stage external_curation.infant_catalog · “infant triage verdict include (0-3 y scope)”
- life stage study.title · “from 11 human infant fecal samples hospitalized”
- life stage study.description · “the microbiome in newborns and the spread”
Evidence examples (one per field × route)
| sample | field | value | route | conf. | source | quote |
|---|---|---|---|---|---|---|
| SRR6257372 | age_at_collection_days | 7 | R2 | 0.75 | paper.supp.table | Day of Life=7 |
| SRR6257418 | age_at_collection_days | 69.0 | R2 | 0.75 | external.microbiomedb source | Age: 69 days |
| SRR6257372 | antibiotic_exposure | yes | R2 | 0.75 | paper.supp.table | Infant antibiotics=yes |
| SRR6257372 | birth_weight_grams | 875 | R2 | 0.75 | paper.supp.table | birthweight=875 |
| SRR6257421 | collection_date | 2012-03 | R1 | 0.85 | biosample.attribute:collection_date | 2012-03 |
| SRR3466404 | country | US | R1 | 0.90 | sample.attr.geo_loc_name | USA: Pittsburgh, PA |
| SRR6257372 | delivery_mode | vaginal | R2 | 0.75 | paper.supp.table | delivery_mode=vaginal |
| SRR3498907 | diet | formula | R2 | 0.85 | paper.supp.41522_2023_392_MOESM1_ESM.xlsx[Supplementary Table 1!Nutrition] | Nutrition: formula-fed |
| SRR6257372 | feeding_mode | exclusive_breast | R2 | 0.75 | paper.supp.table | feeding_practice=breastfed |
| SRR6257372 | gestational_age_weeks | 27.0 | R2 | 0.75 | paper.supp.table | gestational_age_week=27 |
| SRR6257372 | health_condition | preterm_nicu | R2 | 0.70 | paper.supp.table | Pre_term_nec=Preterm |
| SRR6257372 | health_condition_detail | NEC: No | R2 | 0.85 | paper.supp.Table_3.XLSX[mapping_global.txt!NEC] | SRR6257372 | NEC: No |
| SRR3466404 | location_locality | Pittsburgh | R3 | 0.60 | paper.fulltext.results | Magee-Womens’ Hospital of UPMC, Pittsburgh (USA) |
| SRR3466404 | location_site | Magee-Womens' Hospital of UPMC NICU | R3 | 0.60 | paper.fulltext.results | housed in the NICU of the Magee-Womens’ Hospital of UPMC |
| SRR6257372 | nec_status | no | R2 | 0.75 | paper.supp.table | NEC=No |
| SRR6257372 | preterm_status | preterm | R2 | 0.75 | paper.supp.table | Pre_term_nec=Preterm |
| SRR3498907 | sex | female | R2 | 0.85 | paper.supp.41522_2023_392_MOESM1_ESM.xlsx[Supplementary Table 1!Sex] | Sex: female |
| SRR6257418 | sex | male | R2 | 0.75 | external.microbiomedb source | Sex: Male |
| SRR6257418 | subject_id | 011 | R1 | 0.70 | sample.name_rule:library_names | N1_011_069G1 |
| SRR3498907 | subject_id | NIHY1_04 | R2 | 0.85 | paper.supp.41522_2023_392_MOESM1_ESM.xlsx[Supplementary Table 1!ALIAS] | ALIAS: NIHY1_04 |
| SRR6257374 | timepoint_label | 4 | R2 | 0.75 | paper.supp.table | Window=4 |
Sequencing
158 runs over 158 samples · mean 5.79 Gbp per run (median 2.99 Gbp, total 914.77 Gbp; 158 runs with a base count) · layout PAIRED 158 · platform ILLUMINA 158 · models Illumina HiSeq 2000 (158) · 87% of runs with a Sandpiper profile · first public 2016-06-29 – 2017-11-12
Authors (88)
Brooks B first · Olm MR · Firek BA · Baker R · Thomas BC · Morowitz MJ · Banfield JF last · Brown CT first · Xiong W · Firek B · Hettich RL · Bhattacharya N · Crits-Christoph A · Song YS · Zeng S first · Patangia D · Almeida A · Zhou Z · Mu D · Paul Ross R · Stanton C · Wang S last · Casaburi G first · Wei J · Kazi S · Liu J · Wang K · Tao GZ · Lin PY · Dunn JCY · Henrick BM · Frese SA · Sylvester KG last · Peters SL first · Lugli GA first · Mancabelli L · Milani C · Fontana F · Tarracchini C · Alessandri G · van Sinderen D · Turroni F · Ventura M last · Ormaasen I first · Rudi K · Diep DB · Snipen L last · Li S · Ying J · Wang H · Qu Y · Niu X · Xu X first · Feng Q · Zhang T · Gao Y · Cheng Q · Zhang W · Wu Q · Xu K · Li Y · Nguyen N · Taft DH · Mills DA · Lemay DG · Zhu W · Mao S · Zhang A · He W first · Russel J · Klincke F · Nesme J · Sørensen SJ last · Zhang L · Yuan Y · Tian M · Zhou M · Hu Y · Huang J · Zou R · Zhao F · Su X · Liu Q · He Y · Feng J · Huang W · Luo Y · Shen W
Downloads
PRJNA294605.csv.gz (5.8 KB) · parquet (77.3 KB) — all 158 samples, every field with route and confidence · PRJNA294605_determinations.csv.gz (21.6 KB) — 2,397 evidence rows