Evidence map›Paper›PMID 28588252›Full record

ArticleScientific reports2017

Candida albicans Sap6 amyloid regions function in cellular aggregation and zinc binding, and contribute to zinc acquisition.

Rohitashw Kumar, Christine Breindel, Darpan Saraswat, Paul J Cullen, Mira Edgerton

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Article
  2. Metals at the Host-Fungal Pathogen Battleground.Annual review of microbiology · 2024
    Review
  3. Secreted Aspartic Proteinases: Key Factors inInternational journal of molecular sciences · 2024
    Review
  4. Strain and temperature dependent aggregation ofCell surface (Amsterdam, Netherlands) · 2023
    Article
  5. Review
  6. Review
  7. Architecture of the dynamic fungal cell wall.Nature reviews. Microbiology · 2023
    Review
  8. Journal of fungi (Basel, Switzerland) · 2023
    Article
  9. Review
  10. ZnBiomolecules · 2022
    Article
  11. Frontiers in immunology · 2022
    Article
  12. Review
  13. Yeast-Host Interactions:Frontiers in pharmacology · 2021
    Article
  14. Review
  15. Identification and Physicochemical Characterization of a New Allergen fromInternational journal of molecular sciences · 2020
    Article
  16. Zinc at the Host-Fungus Interface: How to Uptake the Metal?Journal of fungi (Basel, Switzerland) · 2020
    Review
  17. Article
  18. Transcription factors and transporters in zinc homeostasis: lessons learned from fungi.Critical reviews in biochemistry and molecular biology · 2020
    Review
  19. The intersection of host and fungus through the zinc lens.Current opinion in microbiology · 2019
    Review
  20. Pathogens (Basel, Switzerland) · 2019
    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

5 authors.

Rohitashw KumarDepartment of Oral Biology, School of Dental Medicine, University at Buffalo, Buffalo, NY, USA.
Christine BreindelDepartment of Oral Biology, School of Dental Medicine, University at Buffalo, Buffalo, NY, USA.
Darpan SaraswatDepartment of Oral Biology, School of Dental Medicine, University at Buffalo, Buffalo, NY, USA.
Paul J CullenDepartment of Biological Sciences, University at Buffalo, Buffalo, NY, USA.
Mira EdgertonDepartment of Oral Biology, School of Dental Medicine, University at Buffalo, Buffalo, NY, USA. edgerto@buffalo.edu.

Funding

Supplements to Support Candida DNA Microarray FacilitiesR01DE010641 · NIDCR · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI EDGERTON, MIRA · 2000 to 2019
$6.7M
Regulation of Candida albicans Pathogenesis by the Signaling Mucin Msb2R01DE022720 · NIDCR · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI CULLEN, PAUL JAMES, EDGERTON, MIRA · 2013 to 2017
$1.9M
NIDCR NIH HHS R01 DE010641NIDCR NIH HHS R01 DE022720
6 · The paper itself

Abstract

Candida albicans is an opportunistic fungal pathogen colonizing the oral cavity. C. albicans secreted aspartic protease Sap6 is important for virulence during oral candidiasis since it degrades host tissues to release nutrients and essential transition metals. We found that zinc specifically increased C. albicans autoaggregation induced by Sap6; and that Sap6 itself bound zinc ions. In silico analysis of Sap6 predicted four amyloidogenic regions that were synthesized as peptides (P1-P4). All peptides, as well as full length Sap6, demonstrated amyloid properties, and addition of zinc further increased amyloid formation. Disruption of amyloid regions by Congo red significantly reduced auotoaggregation. Deletion of C. albicans genes that control zinc acquisition in the ZAP1 regulon, including zinc transporters (Pra1 and Zrt1) and other zinc-regulated surface proteins, resulted in lower autoaggregation and reduction of surface binding of Sap6. Cells with high expression of PRA1 and ZRT1 also showed increased Sap6-mediated autoaggregation. C. albicans ∆sap6 deletion mutants failed to accumulate intracellular zinc comparable to ∆zap1, ∆zrt1, and ∆pra1 cells. Thus Sap6 is a multi-functional molecule containing amyloid regions that promotes autoaggregation and zinc uptake, and may serve as an additional system for the community acquisition of zinc.

Indexed as

Cell AggregationAmyloidogenic ProteinsAspartic Acid EndopeptidasesCandida albicansCarrier ProteinsExtracellular SpaceFungal ProteinsGene Expression RegulationModels, MolecularProtein AggregatesProtein BindingProtein ConformationProtein Interaction Domains and MotifsZincAmyloidogenic ProteinsAspartic Acid EndopeptidasesCarrier ProteinsFungal ProteinsProtein AggregatesSAP6 protein, Candida albicansZinczinc-binding protein

Identifiers

PMID28588252
PMCPMC5460171

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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.