Transcriptome profile of the murine macrophage cell response to Candida parapsilosis

Tibor Németh, Adél Tóth, Zsuzsanna Hamari, András Falus, Katalin Éder, Csaba Vágvölgyi, Allan J. Guimaraes, Joshua D. Nosanchuk, Attila Gácser

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11 Scopus citations

Abstract

Candida parapsilosis is a human fungal pathogen with increasing global significance. Understanding how macrophages respond to C. parapsilosis at the molecular level will facilitate the development of novel therapeutic paradigms. The complex response of murine macrophages to infection with C. parapsilosis was investigated at the level of gene expression using an Agilent mouse microarray. We identified 155 and 511 differentially regulated genes at 3 and 8. h post-infection, respectively. Most of the upregulated genes encoded molecules involved in immune response and inflammation, transcription, signaling, apoptosis, cell cycle, electron transport and cell adhesion. Typical of the classically activated macrophages, there was significant upregulation of genes coordinating the production of inflammatory cytokines such as TNF, IL-1 and IL-15. Further, we used both primary murine macrophages and macrophages differentiated from human peripheral mononuclear cells to confirm the upregulation of the TNF-receptor family member TNFRSF9 that is associated with Th1 T-helper cell responses. Additionally, the microarray data indicate significant differences between the response to C. parapsilosis infection and that of C. albicans.

Original languageEnglish (US)
Pages (from-to)48-56
Number of pages9
JournalFungal Genetics and Biology
Volume65
DOIs
Publication statusPublished - Apr 2014

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Keywords

  • Candida parapsilosis
  • Host response
  • Infection
  • Macrophages

ASJC Scopus subject areas

  • Microbiology
  • Genetics

Cite this

Németh, T., Tóth, A., Hamari, Z., Falus, A., Éder, K., Vágvölgyi, C., ... Gácser, A. (2014). Transcriptome profile of the murine macrophage cell response to Candida parapsilosis. Fungal Genetics and Biology, 65, 48-56. https://doi.org/10.1016/j.fgb.2014.01.006