Evidence map›Paper›PMID 41071924›Full record

ArticleThe Journal of infectious diseases2026

The Gut as a Source of Infection for Fungal Pathogens: Increased Fecal Candida albicans Precedes Onset of Candida Late-Onset Sepsis in Very Preterm Infants.

Rimke R de Kroon, Irini A M Kreulen, Mark Davids, Isabelle A M van Thiel, Iris Admiraal, Xanthe Verdoes, Mirjam M van Weissenbruch, Hendrik J Niemarkt, Wouter J de Jonge, Tim de Meij and 1 more

Abstract readMulticenter Study
In one paragraph

Article in The Journal of infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Rimke R de KroonAmsterdam Reproduction and Development Research Institute, Amsterdam UMC, Amsterdam, the Netherlands.ORCID 0000-0002-7971-3120
Irini A M KreulenAmsterdam Gastroenterology Endocrinology Metabolism Research Institute, Amsterdam UMC, Amsterdam, the  Netherlands.ORCID 0000-0002-6640-8055
Mark DavidsMicrobiota Center Amsterdam, Amsterdam, the  Netherlands.ORCID 0000-0003-3081-9124
Isabelle A M van ThielAmsterdam Reproduction and Development Research Institute, Amsterdam UMC, Amsterdam, the Netherlands.ORCID 0000-0002-8298-9048
Iris AdmiraalTytgat Institute for Liver and Intestinal Research, Amsterdam UMC, University of Amsterdam, Amsterdam, the  Netherlands.
Xanthe VerdoesMicrobiota Center Amsterdam, Amsterdam, the  Netherlands.
Mirjam M van WeissenbruchAmsterdam Reproduction and Development Research Institute, Amsterdam UMC, Amsterdam, the Netherlands.ORCID 0000-0002-8086-9552
Hendrik J NiemarktNeonatal Intensive Care Unit, Maxima Medical Center, Veldhoven, the Netherlands.ORCID 0000-0002-0844-7208
Wouter J de JongeAmsterdam Gastroenterology Endocrinology Metabolism Research Institute, Amsterdam UMC, Amsterdam, the  Netherlands.ORCID 0000-0002-3241-1547
Tim de MeijAmsterdam Reproduction and Development Research Institute, Amsterdam UMC, Amsterdam, the Netherlands.ORCID 0000-0002-7556-5896
generation P study group

Funding

MDL
6 · The paper itself

Abstract

backgroundThe skin-to-blood route is traditionally considered the main pathway in Candida late-onset sepsis (LOS) development in preterm infants. However, emerging evidence suggests that the gut also serves as a source of infection. We aimed to characterize fecal mycobiota and microbiota profiles preceding onset of Candida LOS to assess the role of the preterm gut microbiome in disease development.

methodsThis multicenter case-control study included very preterm infants (<30 weeks of gestation) with Candida LOS. Each case was matched to nonaffected controls by gestational and postnatal age, hospital site, and/or cumulative antibiotic exposure prior to day of LOS onset (t = 0). Fecal samples collected at t = 0 and the 5 preceding days were analyzed by ITS1 and 16S RNA sequencing. Microbial amplicon yields, composition, and interkingdom correlations were assessed.

resultsOf 2397 screened infants, fecal samples were available for 8 of 19 infants with Candida LOS. In these 8 cases, the ITS/16S amplicon yield ratio was increased (P < .001), and the relative abundance of fecal Candida albicans correlated positively with fungal amplicon yield (ρ = 0.71, adjusted P = .005), suggesting increased absolute abundance up to 5 days before onset. Additionally, bacterial yields were significantly lower (P = .02) and α-diversity significantly decreased (P = .012) when compared to the controls.

conclusionsIncreased fecal C albicans preceded Candida LOS onset, implicating the preterm gut as a potential source of infection. Reduced bacterial yields and diversity suggest ecological alterations that may facilitate Candida pathogenicity in the preterm gut. These findings support further research into gut-derived Candida LOS and the potential for microbiota-targeted prevention strategies.

Indexed as

Candida albicansCandidiasisFecesGastrointestinal MicrobiomeSepsisCase-Control StudiesFemaleHumansInfant, NewbornInfant, PrematureMaleRNA, Ribosomal, 16SRNA, Ribosomal, 16SCandidacandidemiafungimicrobial meta-barcodingpreterm colonization

Identifiers

PMID41071924
PMCPMC13017767

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.