Evidence map›Paper›PMID 17074797›Full record

ArticleAntimicrobial agents and chemotherapy2007

Human beta-defensins kill Candida albicans in an energy-dependent and salt-sensitive manner without causing membrane disruption.

Slavena Vylkova, Namrata Nayyar, Wansheng Li, Mira Edgerton

Open access · greenAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

66 citing papers in PubMed, 148 citations in OpenAlex.

  1. Review
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  8. Microorganisms · 2025
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  9. The Contribution of Human Antimicrobial Peptides to Fungi.International journal of molecular sciences · 2025
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  12. Microbiology and molecular biology reviews : MMBR · 2024
    Review
  13. Article
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  15. Microorganisms · 2023
    Article
  16. Review
  17. Article
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  19. Antimicrobial Peptides with Anti-International journal of molecular sciences · 2022
    Review
  20. Article

6 more citing papers are in PubMed but not listed here.

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

4 authors at 2 institutions in 2 countries.

Slavena VylkovaDepartment of Oral Biology, State University of New York at Buffalo, Buffalo, NY 14214, USA.
Namrata Nayyar
Wansheng Li
Mira Edgerton
University at Buffalo, State University of New York · USUniversity of Dental Medicine · MM

Funding

Supplements to Support Candida DNA Microarray FacilitiesR01DE010641 · NIDCR · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI EDGERTON, MIRA · 2000 to 2019
$6.7M
CANDIDACIDAL MECHANISMS OF SALIVARY HISTATINSR29DE010641 · NIDCR · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI EDGERTON, MIRA · 1994 to 1998
–
NIDCR NIH HHS DE10641NIDCR NIH HHS R01 DE010641
6 · The paper itself

Abstract

Human beta-defensin 2 (hBD-2) and hBD-3 have potent fungicidal activity in the micromolar range. Although little is known about their mechanism of action against Candida species, some similarities to the antifungal mechanism of salivary peptide histatin 5 (Hst 5) seem to exist. Since hBD-2 and hBD-3 have been reported to cause direct disruption of target cell membranes, we compared the effects of hBD-2 and hBD-3 on Candida albicans membrane integrity. Incubation of calcein-loaded C. albicans cells with a dose of hBD-2 lethal for 90% of the strains tested (LD(90)) resulted in a maximal dye efflux of only 10.3% +/- 2.8% at 90 min, similar to that induced by Hst 5. In contrast, an LD(90) of hBD-3 more than doubled calcein release from cells yet did not result in more than 24% of total release, showing that neither peptide caused gross membrane damage. As for Hst 5, killing of C. albicans cells by hBD-2 and hBD-3 was salt sensitive; however, Ca(2+) and Mg(2+) inhibited hBD-2 but not hBD-3 fungicidal activity. Pretreatment of C. albicans cells with sodium azide resulted in significantly decreased ATP release and susceptibility of cells to hBD-2 and hBD-3. However, hBD-3 killing was partially restored at concentrations of > or =0.8 microM, showing energy-independent mechanisms at higher doses. C. glabrata resistance to Hst 5, hBD-2, and hBD-3 is not a result of loss of expression of cell wall Ssa proteins. The candidacidal effects of hBD-2-hBD-3 and Hst 5-hBD-2 were additive, while the index of interaction between Hst 5 and hBD-3 was 0.717 (P < 0.05). Thus, the candidacidal action of hBD-2 shows many similarities to that of Hst 5 in terms of salt sensitivity, ion selectivity, and energy requirements while hBD-3 exhibits biphasic concentration-dependent mechanisms of candidacidal action complementary to those of Hst 5.

Indexed as

Adenosine TriphosphateAntifungal Agentsbeta-DefensinsBlotting, WesternCalcium ChlorideCandida albicansCell MembraneCell WallDose-Response Relationship, DrugHistatinsHumansPhosphatesSalivary Proteins and PeptidesSodium ChlorideAdenosine TriphosphateAntifungal Agentsbeta-DefensinsCalcium ChlorideDEFB103A protein, humanHistatinsHTN3 protein, humanPhosphatesSalivary Proteins and PeptidesSodium Chloridesodium phosphate

Identifiers

PMID17074797
PMCPMC1797696
OpenAlexW2076519123

What OpenQuestion holds

Textmetadata
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.