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

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...

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Autores principales: Azimova, Dinara, Herrera, Nadia, Duvenage, Lucian, Voorhies, Mark, Rodriguez, Rosa A., English, Bevin C., Hoving, Jennifer C., Rosenberg, Oren, Sil, Anita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9255746/
https://www.ncbi.nlm.nih.gov/pubmed/35731824
http://dx.doi.org/10.1371/journal.ppat.1010417
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author Azimova, Dinara
Herrera, Nadia
Duvenage, Lucian
Voorhies, Mark
Rodriguez, Rosa A.
English, Bevin C.
Hoving, Jennifer C.
Rosenberg, Oren
Sil, Anita
author_facet Azimova, Dinara
Herrera, Nadia
Duvenage, Lucian
Voorhies, Mark
Rodriguez, Rosa A.
English, Bevin C.
Hoving, Jennifer C.
Rosenberg, Oren
Sil, Anita
author_sort Azimova, Dinara
collection PubMed
description 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.
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spelling pubmed-92557462022-07-06 Cbp1, a fungal virulence factor under positive selection, forms an effector complex that drives macrophage lysis Azimova, Dinara Herrera, Nadia Duvenage, Lucian Voorhies, Mark Rodriguez, Rosa A. English, Bevin C. Hoving, Jennifer C. Rosenberg, Oren Sil, Anita PLoS Pathog Research Article 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. Public Library of Science 2022-06-22 /pmc/articles/PMC9255746/ /pubmed/35731824 http://dx.doi.org/10.1371/journal.ppat.1010417 Text en © 2022 Azimova et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Azimova, Dinara
Herrera, Nadia
Duvenage, Lucian
Voorhies, Mark
Rodriguez, Rosa A.
English, Bevin C.
Hoving, Jennifer C.
Rosenberg, Oren
Sil, Anita
Cbp1, a fungal virulence factor under positive selection, forms an effector complex that drives macrophage lysis
title Cbp1, a fungal virulence factor under positive selection, forms an effector complex that drives macrophage lysis
title_full Cbp1, a fungal virulence factor under positive selection, forms an effector complex that drives macrophage lysis
title_fullStr Cbp1, a fungal virulence factor under positive selection, forms an effector complex that drives macrophage lysis
title_full_unstemmed Cbp1, a fungal virulence factor under positive selection, forms an effector complex that drives macrophage lysis
title_short Cbp1, a fungal virulence factor under positive selection, forms an effector complex that drives macrophage lysis
title_sort cbp1, a fungal virulence factor under positive selection, forms an effector complex that drives macrophage lysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9255746/
https://www.ncbi.nlm.nih.gov/pubmed/35731824
http://dx.doi.org/10.1371/journal.ppat.1010417
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