A Pseudomonas aeruginosa quorum‐sensing molecule influences Candida albicans morphology
Open accessAbstract
Summary: Candida albicans is an opportunistic pathogen that is commonly found as a member of the human microflora. The ability of C. albicans to alter its cellular morphology has been associated with its virulence; yeast cells are more prevalent in commensal interactions whereas filamentous cells appear important in opportunistic infections. C. albicans encounters a multitude of other microbial species in the host environment and it is likely that they impact the C. albicans transition between virulent and non‐virulent states. Here, we report that C. albicans morphology is significantly affected by the presence of Pseudomonas aeruginosa , another opportunistic pathogen. In a screen using a C. albicans HWP1–lacZ strain to indicate regions of filamentous growth, we identified P. aeruginosa mutants incapable of inhibiting C. albicans filamentation. Through these studies, we found that 3‐oxo‐C12 homoserine lactone, a cell–cell signalling molecule produced by P. aeruginosa , was sufficient to inhibit C. albicans filamentation without affecting fungal growth rates. Both microscopic analysis and real‐time reverse transcription polymerase chain reaction analysis of morphology‐specific markers confirmed that filamentation was suppressed by 200 µM 3‐oxo‐C12 homoserine lactone. Structurally related compounds with a 12‐carbon chain length, e.g. C12‐acyl homoserine lactone and dodecanol also affected C. albicans filamentation at similar concentrations. In contrast, other acylated homoserine lactones of different chain lengths did not affect fungal morphology. The activity of 3OC12HSL is compared with that of farnesol, a C. albicans ‐produced molecule also with a C12‐backbone. The effects that bacteria have on the morphology of C. albicans represents one of the ways by which bacteria can influence the behaviour of fungal cells.
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Pseudomonas aeruginosa secretes a 12-carbon acyl homoserine lactone that modulates hyphal growth by Candida albicans.
“For example, P. aeruginosa secretes a 12-carbon acyl homoserine lactone that modulates hyphal growth by C. albicans (78).”
From <i>Candida albicans</i> Biofilms and Human Disease (2015) · cites this paper as [78]
Candida albicans interacts with several bacterial species found in the gut, such as Enterococcus and Escherichia species; those found in the vagina, such as Lactobacillus species; and those found in the lungs of patients with cystic fibrosis, such as Pseudomonas aeruginosa.
“C. albicans also interacts with several bacterial species found in the gut, such as Enterococcus and Escherichia species; those found in the vagina, such as Lactobacillus species; and those found in the lungs of patients with cystic fibrosis, such as Pseudomonas aeruginosa (13, 34, 54, 78).”
From <i>Candida albicans</i> Biofilms and Human Disease (2015) · cites this paper as [78]
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- Authors
- Hogan, D. A., Vik, Å., & Kolter, R.
- Affiliations
- Dartmouth College (US)
- Harvard University (US)
- Corresponding author
- Kolter, Roberto
- Venue
- Molecular Microbiology
- Publisher
- Wiley
- Published
- 2004-10-15
- Volume
- 54
- Issue
- 5
- Pages
- 1212-1223
- ISSN
- 0950-382X (ISSN-L)
- 1365-2958
- OpenAlex
- W1776282777
- Cited by
- 575
- References
- 54
- Citations by year
- 2026: 18 · 2025: 6 · 2024: 11 · 2023: 29 · 2022: 20 · 2021: 39 · 2020: 33 · 2019: 23 · 2018: 26 · 2017: 37 · 2016: 32 · 2015: 35 · 2014: 37 · 2013: 30 · 2012: 30
- FWCI
- 6.39
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Molecular Microbiology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Norges Forskningsråd
- National Institutes of Health
- National Heart, Lung, and Blood Institute
- National Institute of General Medical Sciences (R01GM058213, GM58213)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bacterial biofilms and quorum sensing
- Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Keywords
- Candida albicans, Pseudomonas aeruginosa, quorum sensing, yeast-to-hypha transition, fungal-bacterial interactions, N-acyl homoserine lactones, farnesol, opportunistic pathogens, virulence
- MeSH terms
- Antifungal Agents, beta-Galactosidase, Candida albicans, Farnesol, Genes, Bacterial, Genes, Fungal, Homoserine, Dodecanol, Microscopy, Mutation, Pseudomonas aeruginosa, Recombinant Fusion Proteins, RNA, Fungal, RNA, Messenger, Transcription, Genetic, 4-Butyrolactone, Gene Expression Regulation, Fungal, Genes, Reporter, Reverse Transcriptase Polymerase Chain Reaction
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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