Evidence map›Paper›PMID 27303684›Full record

ArticlemSphere

Manipulation of Host Diet To Reduce Gastrointestinal Colonization by the Opportunistic Pathogen Candida albicans.

Kearney T W Gunsalus, Stephanie N Tornberg-Belanger, Nirupa R Matthan, Alice H Lichtenstein, Carol A Kumamoto

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in mSphere. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03630770 (Effect of Medium Chain Triglyceride Intake on Colonization of Preterm Infants With Candida), which is not on this map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
2.1field-weighted citation impact, top 13% of its field
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.

NCT03630770 phase1completednot on this map

Effect of Medium Chain Triglyceride Intake on Colonization of Preterm Infants With Candida

TypeinterventionalSponsorJoseph BlissRan2014 to 2021Enrolled12ConditionsCandida Infection, Premature InfantArmsMedium-Chain Triglyceride (MCT) Oil
3 · Its place in the literature

Who cites it

46 citing papers in PubMed, 81 citations in OpenAlex.

  1. Trial
  2. Trial
  3. bioRxiv : the preprint server for biology · 2026
    Article
  4. Article
  5. Article
  6. Sensitive and rapid detection ofFrontiers in cellular and infection microbiology · 2026
    Article
  7. The pathogenicity and future treatment strategies ofFrontiers in cellular and infection microbiology · 2026
    Review
  8. International journal of microbiology · 2026
    Article
  9. Article
  10. Article
  11. Review
  12. Infection and immunity · 2025
    Review
  13. Commensal colonization ofMicrobiology spectrum · 2025
    Article
  14. Review
  15. Review
  16. Review
  17. Rapid and simple detection ofFrontiers in cellular and infection microbiology · 2025
    Article
  18. Review
  19. Anti-Infection of Oral Microorganisms from Herbal Medicine ofDrug design, development and therapy · 2024
    Review
  20. Article
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

5 authors at 1 institution in 1 country.

Kearney T W GunsalusTraining in Education and Critical Research Skills (TEACRS) Program, Tufts University, Boston, Massachusetts, USA; Department of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, Massachusetts, USA.ORCID 0000-0001-6022-3159
Stephanie N Tornberg-BelangerDepartment of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, Massachusetts, USA.
Nirupa R MatthanJean Mayer USDA Human Nutrition Research Center, Cardiovascular Nutrition Laboratory, Tufts University, Boston, Massachusetts, USA.
Alice H LichtensteinJean Mayer USDA Human Nutrition Research Center, Cardiovascular Nutrition Laboratory, Tufts University, Boston, Massachusetts, USA.
Carol A KumamotoDepartment of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, Massachusetts, USA.
Tufts University · US

Funding

Tufts Clinical and Translational Research InstituteUL1TR001064 · NCATS · TUFTS UNIVERSITY BOSTON · PI SELKER, HARRY P. · 2013 to 2017
$26.4M
TUFTS CLINICAL AND TRANSLATION SCIENCE INSTITUTE (UL1): BPCAUL1RR025752 · NCRR · TUFTS UNIVERSITY BOSTON · PI SELKER, HARRY P. · 2008 to 2011
$17.6M
Training in Education and Critical Research SkillsK12GM074869 · NIGMS · TUFTS UNIVERSITY BOSTON · PI MOORE, CLAIRE L · 2006 to 2017
$8.5M
Tufts Clinical and Translation Science Institute (UL1)UL1TR000073 · NCATS · TUFTS UNIVERSITY BOSTON · PI SELKER, HARRY P. · 2012 to 2013
$5.5M
Contact sensing and C. albicans-host interactionR01AI081794 · NIAID · TUFTS UNIVERSITY BOSTON · PI KUMAMOTO, CAROL A. · 2010 to 2014
$2.2M
NCATS NIH HHS UL1 TR000073NCATS NIH HHS UL1 TR001064NCRR NIH HHS UL1 RR025752NIAID NIH HHS R01 AI081794NIGMS NIH HHS K12 GM074869
6 · The paper itself

Abstract

Candida albicans, the most common human fungal pathogen, can cause systemic infections with a mortality rate of ~40%. Infections arise from colonization of the gastrointestinal (GI) tract, where C. albicans is part of the normal microflora. Reducing colonization in at-risk patients using antifungal drugs prevents C. albicans-associated mortalities. C. albicans provides a clinically relevant system for studying the relationship between diet and the microbiota as it relates to commensalism and pathogenicity. As a first step toward a dietary intervention to reduce C. albicans GI colonization, we investigated the impact of dietary lipids on murine colonization by C. albicans. Coconut oil and its constituent fatty acids have antifungal activity in vitro; we hypothesized that dietary coconut oil would reduce GI colonization by C. albicans. Colonization was lower in mice fed a coconut oil-rich diet than in mice fed diets rich in beef tallow or soybean oil. Switching beef tallow-fed mice to a coconut oil diet reduced preexisting colonization. Coconut oil reduced colonization even when the diet also contained beef tallow. Dietary coconut oil also altered the metabolic program of colonizing C. albicans cells. Long-chain fatty acids were less abundant in the cecal contents of coconut oil-fed mice than in the cecal contents of beef tallow-fed mice; the expression of genes involved in fatty acid utilization was lower in C. albicans from coconut oil-fed mice than in C. albicans from beef tallow-fed mice. Extrapolating to humans, these findings suggest that coconut oil could become the first dietary intervention to reduce C. albicans GI colonization. IMPORTANCE Candida albicans, the most common human fungal pathogen, can cause infections with a mortality rate of ~40%. C. albicans is part of the normal gut flora, but when a patient's immune system is compromised, it can leave the gut and cause infections. By reducing the amount of C. albicans in the gut of susceptible patients, infections (and the resulting fatalities) can be prevented. Currently, this is done using antimicrobial drugs; to "preserve" drugs for treating infections, we looked for a dietary change to reduce the amount of C. albicans in the gut. Using a mouse model, we showed that adding coconut oil to the diet could become the first drug-free way to reduce C. albicans in the gut. More broadly, this model lets us study the interactions between our diet and the microbes in our body and the reasons why some of those microbes, under certain conditions, cause disease. Podcast: A podcast concerning this article is available.

Indexed as

CandidaCandida albicanscarbon metabolismcommensalfatty acidshost-pathogen interactionsmedium-chain fatty acidsmicrobiomepathogenesis

Identifiers

PMID27303684
PMCPMC4863630
OpenAlexW2330188318

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.