Evidence map›Paper›PMID 20361054›Full record

ArticlePLoS pathogens2010

Serological profiling of a Candida albicans protein microarray reveals permanent host-pathogen interplay and stage-specific responses during candidemia.

A Brian Mochon, Ye Jin, Jin Ye, Matthew A Kayala, John R Wingard, Cornelius J Clancy, M Hong Nguyen, Philip Felgner, Pierre Baldi, Haoping Liu

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.7field-weighted citation impact, top 6% 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.

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

40 citing papers in PubMed, 82 citations in OpenAlex.

  1. AbioRxiv : the preprint server for biology · 2026
    Article
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  3. Review
  4. mBio · 2025
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  5. Glycan microarray analysis ofProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Article
  7. Review
  8. Deletion ofmSphere · 2025
    Article
  9. Review
  10. Review
  11. Commensal fungi in intestinal health and disease.Nature reviews. Gastroenterology & hepatology · 2023
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. The Role ofFrontiers in cellular and infection microbiology · 2021
    Review
  18. Developments and Applications of Functional Protein Microarrays.Molecular & cellular proteomics : MCP · 2020
    Review
  19. Review
  20. Article
4 · The record

Corrections and comments

  • Erratum issued
    Ye, Jin [corrected to Jin, Ye]
5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

A Brian MochonDepartment of Biological Chemistry, University of California Irvine, Irvine, California, United States of America.
Ye Jin
Jin Ye
Matthew A Kayala
John R Wingard
Cornelius J Clancy
M Hong Nguyen
Philip Felgner
Pierre Baldi
Haoping Liu
University of California, Irvine · USUniversity of Pittsburgh · USUniversity of Florida · US

Funding

Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Melanie Funes · 1994 to 2026
$57.9M
Mycology Research Unit: In Vivo Induced Fungal AntigensP01AI061537 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WINGARD, JOHN R. · 2004 to 2008
$3.7M
NCI NIH HHS P30 CA062203NIAID NIH HHS P01 AI061537NIAID NIH HHS P01AI061537NIAID NIH HHS R01GM/AI55155
6 · The paper itself

Abstract

Candida albicans in the immunocompetent host is a benign member of the human microbiota. Though, when host physiology is disrupted, this commensal-host interaction can degenerate and lead to an opportunistic infection. Relatively little is known regarding the dynamics of C. albicans colonization and pathogenesis. We developed a C. albicans cell surface protein microarray to profile the immunoglobulin G response during commensal colonization and candidemia. The antibody response from the sera of patients with candidemia and our negative control groups indicate that the immunocompetent host exists in permanent host-pathogen interplay with commensal C. albicans. This report also identifies cell surface antigens that are specific to different phases (i.e. acute, early and mid convalescence) of candidemia. We identified a set of thirteen cell surface antigens capable of distinguishing acute candidemia from healthy individuals and uninfected hospital patients with commensal colonization. Interestingly, a large proportion of these cell surface antigens are involved in either oxidative stress or drug resistance. In addition, we identified 33 antigenic proteins that are enriched in convalescent sera of the candidemia patients. Intriguingly, we found within this subset an increase in antigens associated with heme-associated iron acquisition. These findings have important implications for the mechanisms of C. albicans colonization as well as the development of systemic infection.

Indexed as

Protein Array AnalysisAntibodies, FungalAntigens, FungalBiomarkersCandida albicansCandidiasisConvalescenceHemeHost-Pathogen InteractionsHumansImmunoglobulin GSeroepidemiologic StudiesAntibodies, FungalAntigens, FungalBiomarkersHemeImmunoglobulin G

Identifiers

PMID20361054
PMCPMC2845659
OpenAlexW2106208567

What OpenQuestion holds

Textmetadata
LicenceCC0
Read underepoch 390

Registered trials

None linked

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.