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Using a Bacterial Pathogen to Probe for Cellular and Organismic-level Host Responses
Published on: February 22, 2019
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.
Abstract:
Intracellular pathogens secrete effectors to manipulate their host cells. Histoplasma capsulatum (Hc) is a fungal intracellular pathogen of humans that grows in a yeast form in the host. Hc yeasts are phagocytosed by macrophages, where fungal intracellular replication precedes macrophage lysis. The most abundant virulence factor secreted by Hc yeast cells is Calcium Binding Protein 1 (Cbp1), which is absolutely required for macrophage lysis. Here we take an evolutionary, structural, and cell biological approach to understand Cbp1 function. We find that Cbp1 is present only in the genomes of closely related dimorphic fungal species of the Ajellomycetaceae family that lead primarily intracellular lifestyles in their mammalian hosts (Histoplasma, Paracoccidioides, and Emergomyces), but not conserved in the extracellular fungal pathogen Blastomyces dermatitidis. We observe a high rate of fixation of non-synonymous substitutions in the Cbp1 coding sequences, indicating that Cbp1 is under positive selection. We determine the de novo structures of Hc H88 Cbp1 and the Paracoccidioides americana (Pb03) Cbp1, revealing a novel "binocular" fold consisting of a helical dimer arrangement wherein two helices from each monomer contribute to a four-helix bundle. In contrast to Pb03 Cbp1, we show that Emergomyces Cbp1 orthologs are unable to stimulate macrophage lysis when expressed in the Hc cbp1 mutant. Consistent with this result, we find that wild-type Emergomyces africanus yeast are able to grow within primary macrophages but are incapable of lysing them. Finally, we use subcellular fractionation of infected macrophages and indirect immunofluorescence to show that Cbp1 localizes to the macrophage cytosol during Hc infection, making this the first instance of a phagosomal human fungal pathogen directing an effector into the cytosol of the host cell. We additionally show that Cbp1 forms a complex with Yps-3, another known Hc virulence factor that accesses the cytosol. Taken together, these data imply that Cbp1 is a fungal virulence factor under positive selection that localizes to the cytosol to trigger host cell lysis.
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.

