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

Author:

Azimova DinaraORCID,Herrera NadiaORCID,Duvenage LucianORCID,Voorhies Mark,Rodriguez Rosa A.,English Bevin C.ORCID,Hoving Jennifer C.,Rosenberg Oren,Sil AnitaORCID

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.Hcyeasts are phagocytosed by macrophages, where fungal intracellular replication precedes macrophage lysis. The most abundant virulence factor secreted byHcyeast 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, andEmergomyces), but not conserved in the extracellular fungal pathogenBlastomyces 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 thede novostructures ofHc H88 Cbp1 and theParacoccidioides 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 thatEmergomycesCbp1 orthologs are unable to stimulate macrophage lysis when expressed in theHc cbp1mutant. Consistent with this result, we find that wild-typeEmergomyces africanusyeast 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 duringHcinfection, 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 knownHcvirulence 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.

Funder

National Institute of Allergy and Infectious Diseases

UCSF Pulmonary Division Training Grant

Burroughs Wellcome Fund

Office of the President, University of California

Chan-Zuckerberg Biohub

University of Cape Town

Wellcome Trust

Carnegie Corporation

University of California

National Institutes of Health

Plexxikon

US Department of Energy Office of Biological and Environmental Research

US Department of Energy

Publisher

Public Library of Science (PLoS)

Subject

Virology,Genetics,Molecular Biology,Immunology,Microbiology,Parasitology

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