Cell-type-specific transcriptional profiles of the dimorphic pathogen Penicillium marneffei reflect distinct

Shivani Pasricha1, Michael Payne, David Canovas

  • 1Department of Genetics, University of Melbourne, Victoria 3010, Australia.

G3 (Bethesda, Md.)
|September 25, 2013
PubMed

Insights

Penicillium marneffei undergoes temperature-dependent dimorphic switching between hyphal and yeast forms. Understanding gene expression during this switch reveals key genes like ergM, crucial for pathogenicity and antifungal drug sensitivity.

Area of Science:

  • Mycology
  • Medical Mycology
  • Molecular Biology

Background:

  • Penicillium marneffei is an opportunistic pathogen causing infections in Southeast Asia.
  • The fungus exhibits dimorphic switching, existing as a filamentous hyphal form at 25°C and a pathogenic yeast form at 37°C.

Purpose of the Study:

  • To investigate the gene expression profiles during dimorphic switching in Penicillium marneffei.
  • To identify genes associated with specific cell states (hyphal, yeast, conidiation) and the transition between them.

Main Methods:

  • Two microarray-based gene expression profiling experiments were conducted.
  • Experiment 1 compared gene expression in hyphal, yeast, and conidiation phases.
  • Experiment 2 analyzed gene expression during the morphological transition between cell types.

Main Results:

  • Differential gene expression was identified and clustered by function and expression patterns.
  • The ergosterol biosynthesis gene ergM showed higher expression in the yeast form and its deletion caused growth defects and antifungal sensitivity.
  • Genes were classified based on spatio-temporal expression patterns during the dimorphic switch.

Conclusions:

  • Gene expression profiling provides insights into the molecular mechanisms of dimorphic switching in Penicillium marneffei.
  • The ergM gene plays a significant role in yeast morphogenesis and azole antifungal susceptibility.
  • Classifying genes by expression patterns aids in understanding their role in fungal pathogenicity.

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