Cited by 69Fungal and yeast genetics researchAntifungal resistance and susceptibilityFungal Infections and Studies

Genes involved in β‐oxidation, energy metabolism and glyoxylate cycle are induced by Candida albicans during macrophage infection

Prigneau, Odile, Porta, Amalia, Poudrier, Jacques A., Colonna‐Romano, Sergio, Noël, Thierry, Maresca, Bruno·2003·Yeast

Abstract

The ability of intracellular pathogens to cause infection is related to their capacity to survive and grow inside macrophages or in other cell types. Candida albicans latent virulence is likely to be related to a similar mechanism of avoiding killing by specialized cells and to the resulting ability to grow in such hostile environments. Using a differential display reverse transcription polymerase chain reaction technique, we have identified seven genes induced in C. albicans during macrophage phagocytosis. Sequence analyses and database searches revealed that these cDNAs coded for proteins homologous to yeast metabolic proteins. Interestingly, four of them are putative peroxisomal proteins, and two are involved in environmental signal sensing and transduction. Among the seven genes induced by C. albicans, six represent new information that were not described in other infection models.

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Crossref · 10.1002/yea.998

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  • When C. albicans cells face a glucose-poor niche their metabolism changes; after phagocytosis by macrophages, repression of glycolysis occurs, and the glyoxylate cycle, gluconeogenesis, and β-oxidation are induced.

    “When C. albicans cells face a glucose-poor niche their metabolism changes. For instance, after phagocytosis of C. albicans by macrophages, repression of glycolysis occurs, the glyoxylate cycle, gluconeogenesis, and β-oxidation (Fradin et al., 2003, 2005; Prigneau et al., 2003; Lorenz et al., 2004; Barelle et al., 2006; Wilson et al., 2009) are induced.”

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Authors
Prigneau, O., Porta, A., Poudrier, J. A., Colonna‐Romano, S., Noël, T., & Maresca, B.
Affiliations
  • Institute of Genetics and Biophysics (IT)
  • University of Salerno (IT)
  • Université Paris Descartes (FR)
Corresponding author
Maresca, Bruno
Venue
Yeast
Publisher
Wiley
Published
2003-05-15
Volume
20
Issue
8
Pages
723-730
ISSN
  • 0749-503X (ISSN-L)
  • 1097-0061
OpenAlex
W2073175848
Cited by
69
References
18
Citations by year
2026: 2 · 2025: 1 · 2023: 1 · 2022: 1 · 2021: 4 · 2020: 3 · 2019: 1 · 2016: 1 · 2015: 2 · 2014: 10 · 2012: 2
FWCI
2.41
Type
journal article
Language
en
Open access
closed
Locations
  • Yeast (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Ministero dell' Università, Italy
  • Ministero della Sanità-Istituto Superiore di Sanità, Progetto AIDS, Italy
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
  • Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
  • Health Sciences › Medicine › Epidemiology › Fungal Infections and Studies
Keywords
Candida albicans, macrophage infection, phagocytosis, gene induction, fatty acid beta-oxidation, energy metabolism, glyoxylate cycle, peroxisomal proteins, transduction, virulence, differential display
MeSH terms
Candida albicans, Candidiasis, Cloning, Molecular, Energy Metabolism, Genes, Fungal, Glyoxylates, Humans, Macrophages, Oxidation-Reduction, Phagocytosis, RNA, Fungal, Blotting, Northern, Gene Expression Regulation, Fungal, Polymerase Chain Reaction, Sequence Analysis, DNA, Peroxisomes, Gene Expression Profiling

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