Cbp1, a fungal virulence factor under positive selection, forms an effector complex that drives macrophage lysis

Dinara Azimova1, Nadia Herrera1, Lucian Duvenage2

  • 1University of California San Francisco, San Francisco, California, United States of America.

Plos Pathogens
|June 22, 2022
PubMed

Insights

Calcium Binding Protein 1 (Cbp1) is a fungal virulence factor essential for Histoplasma capsulatum to lyse host macrophages. This study reveals Cbp1’s unique structure, evolutionary selection, and cytosolic localization, explaining its role in fungal pathogenesis.

Area of Science:

  • Mycology and Pathogen Biology
  • Molecular and Structural Biology
  • Evolutionary Biology

Background:

  • Intracellular fungal pathogens like Histoplasma capsulatum (Hc) manipulate host cells for survival and replication.
  • Hc yeasts are phagocytosed by macrophages, replicate intracellularly, and cause host cell lysis.
  • Calcium Binding Protein 1 (Cbp1) is a key Hc virulence factor, essential for macrophage lysis.

Purpose of the Study:

  • To understand the function of Cbp1 through evolutionary, structural, and cell biological analyses.
  • To investigate the conservation and selection pressures on Cbp1 across related fungal species.
  • To determine the subcellular localization and mechanism of Cbp1-mediated host cell lysis.

Main Methods:

  • Comparative genomics to assess Cbp1 conservation in Ajellomycetaceae family fungi.
  • Sequence analysis to identify positive selection on Cbp1 coding sequences.
  • De novo structure determination of Hc and Paracoccidioides Cbp1.
  • Functional assays using Hc mutants and heterologous expression of Cbp1 orthologs.
  • Subcellular fractionation and immunofluorescence microscopy to determine Cbp1 localization.

Main Results:

  • Cbp1 is conserved in intracellularly adapted Ajellomycetaceae (Histoplasma, Paracoccidioides, Emergomyces) but absent in extracellular Blastomyces.
  • Cbp1 sequences show evidence of positive selection, indicating rapid evolution.
  • Novel 'binocular' fold structure determined for Hc and Paracoccidioides Cbp1.
  • Emergomyces Cbp1 orthologs and wild-type Emergomyces africanus do not induce macrophage lysis.
  • Cbp1 localizes to the macrophage cytosol during Hc infection, a novel mechanism for fungal effectors.
  • Cbp1 forms a complex with another cytosolic effector, Yps-3.

Conclusions:

  • Cbp1 is an evolutionarily selected virulence factor unique to intracellularly adapted dimorphic fungi.
  • Its novel structure and cytosolic localization are critical for triggering host macrophage lysis.
  • Cbp1 represents a novel class of fungal effectors that directly manipulate the host cell cytoplasm.