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PRJNA717139 SRP318065

C. parapsilosis genomics in premature infant gut microbiome

Genetic and behavioral adaptation of Candida parapsilosis to the microbiome of hospitalized infants revealed by in situ genomics, transcriptomics and proteomics

18 fecal samples from neonates and infants at Magee-Womens Hospital, Pittsburgh, PA, analyzed for Candida parapsilosis genome diversity and in situ gene expression; case series design. machine-written summary

18 samples · 18 runs · US · Infant / toddler · 2021 · 12.89 Gbp / sample

Sources
✓Sequence archive 54○Abstract / description✓Full text 54○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 archive54 sample values (age, collection date, country)
○ Abstract / descriptionread; no usable statement
✓ Full text54 sample values (location locality, location region, location site) · PMC8215838
○ Supplementary tablesfiles read; no table could be matched to the samples
– External resourcesnot covered by the external resources we ingest
– User contributionnothing uploaded yet
– Human verifiednot yet checked by a person · I checked this project — verify it
Samples at a glance
1 country
Age
infant9
neonate9
Country
US18
Body site
primary18
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 %)this project, 0.3–1 Gbp: 1 samplesall projects, 1–3 Gbp: 124,983 samples (22 %)this project, 1–3 Gbp: 3 samplesall projects, 3–10 Gbp: 253,728 samples (44 %)this project, 3–10 Gbp: 4 samplesall projects, 10–30 Gbp: 72,533 samples (13 %)this project, 10–30 Gbp: 10 samplesall 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 12.89 Gbp per sample0130Gbp
Community composition
Enterococcus 65.6%Staphylococcus 12.3%Lactobacillus 5.2%Citrobacter_A 2.0%Corynebacterium 0.2%Enterococcus_L 0.0%Enterococcus_C 0.0%Enterococcus_B 0.0%Enterococcus_A 0.0%not assigned to a genus 14.7%

Genera, mean relative abundance over 17 profiled gut samples of this project (Sandpiper SingleM profiles, GTDB R232; low-depth and non-metagenome profiles left out).

Field coverage
fieldsamplescoverageR1R2R3R4
age_category18 100%
country18 100%18
health_condition0 0%
subject_id0 0%
age_at_collection_days18 100%18
collection_date18 100%18
detailed_location18 100%
location_locality18 100%18
location_region18 100%18
location_site18 100%18
Papers (1)
  • Genetic and behavioral adaptation of Candida parapsilosis to the microbiome of hospitalized infants revealed by in situ genomics, transcriptomics, and proteomics. PMID 34154658 PMC8215838 curated
Details
Archive description

Candida parapsilosis is a common cause of invasive candidiasis, especially in newborn infants, and infections have been increasing over the past two decades. C. parapsilosis has been primarily studied in pure culture, leaving gaps in understanding of its function in a microbiome context. Here, we compare five unique C. parapsilosis genomes assembled from premature infant fecal samples, three of which are newly reconstructed, and analyze their genome structure, population diversity and in situ activity relative to reference strains in pure culture. All five genomes contain hotspots of single nucleotide variants, some of which are shared by strains from multiple hospitals. A subset of environmental and hospital-derived genomes share variants within these hotspots suggesting derivation of that region from a common ancestor. Four of the newly reconstructed C. parapsilosis genomes have four to sixteen copies of the gene RTA3, which encodes a lipid translocase and is implicated in antifungal resistance, potentially indicating adaptation to hospital antifungal use. Time course metatranscriptomics and metaproteomics on fecal samples from a premature infant with a C. parapsilosis blood infection revealed highly variable in situ expression patterns that are distinct from those of similar strains in pure cultures. For example, biofilm formation genes were relatively less expressed in situ, whereas genes linked to oxygen utilization were more highly expressed, indicative of growth in a relatively aerobic environment. In gut microbiome samples, C. parapsilosis coexisted with Enterococcus faecalis that shifted in relative abundance over time, accompanied by changes in bacterial and fungal gene expression and proteome composition. The results reveal potentially medically relevant differences in Candida function in gut vs. laboratory environments, and constrain evolutionary processes that could contribute to hospital strain persistence and transfer into premature infant microbiomes.

How this project entered the registry

Classified as human gut / stool / blood / tissue / internal fluids 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.description · “from premature infant fecal samples, three of”
  • body site external_curation.infant_catalog · “infant triage verdict include (gut/stool scope)”
  • body site study.description · “a C. parapsilosis blood infection revealed highly”
  • life stage external_curation.infant_catalog · “infant triage verdict include (0-3 y scope)”
  • life stage study.title · “microbiome of hospitalized infants revealed by in”
  • life stage study.description · “candidiasis, especially in newborn infants, and infections”
Evidence examples (one per field × route)
samplefieldvaluerouteconf.sourcequote
SAMN18948219age_at_collection_days12R10.90biosample_attr12
SAMN18948219collection_date2017R10.85biosample.attribute:collection_datecollection_date: 2017
SAMN18948219countryUSR10.90biosample_attrUSA: Magee-Womens Hospital, Pittsburgh, PA
SAMN18948219location_localityPittsburghR30.70paper.fulltext.methodsMagee-Womens Hospital (Pittsburgh, PA)
SAMN18948219location_regionPennsylvaniaR30.70paper.fulltext.methodsMagee-Womens Hospital (Pittsburgh, PA)
SAMN18948219location_siteMagee-Womens HospitalR30.70paper.fulltext.methodshoused in the Magee-Womens Hospital (Pittsburgh, PA)
Sequencing

18 runs over 18 samples · mean 12.06 Gbp per run (median 12.89 Gbp, total 217.01 Gbp; 18 runs with a base count) · layout PAIRED 18 · platform ILLUMINA 18 · models Illumina NovaSeq 6000 (18) · 94% of runs with a Sandpiper profile · first public 2021-08-25

Authors (12)

West PT first · Peters SL · Olm MR · Yu FB · Gause H · Lou YC · Firek BA · Baker R · Johnson AD · Morowitz MJ · Hettich RL · Banfield JF last

Downloads

PRJNA717139.csv.gz (1.4 KB) · parquet (70.4 KB) — all 18 samples, every field with route and confidence · PRJNA717139_determinations.csv.gz (1.1 KB) — 108 evidence rows

Samples (18 · every field this project has values for · hover a cell for its source)
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