Distinct Spatiotemporal Distribution of Bacterial Toxin-Produced Cellular cAMP Differentially Inhibits Opsonophagocytic Signaling

Myeloid phagocytes have evolved to rapidly recognize invading pathogens and clear them through opsonophagocytic killing. The adenylate cyclase toxin (CyaA) of <i>Bordetella pertussis</i> and the edema toxin (ET) of <i>Bacillus anthracis</i> are both calmodulin-activated toxin...

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Main Authors: Shakir Hasan, Waheed Ur Rahman, Peter Sebo, Radim Osicka
Format: Article
Language:English
Published: MDPI AG 2019-06-01
Series:Toxins
Subjects:
Online Access:https://www.mdpi.com/2072-6651/11/6/362
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author Shakir Hasan
Waheed Ur Rahman
Peter Sebo
Radim Osicka
author_facet Shakir Hasan
Waheed Ur Rahman
Peter Sebo
Radim Osicka
author_sort Shakir Hasan
collection DOAJ
description Myeloid phagocytes have evolved to rapidly recognize invading pathogens and clear them through opsonophagocytic killing. The adenylate cyclase toxin (CyaA) of <i>Bordetella pertussis</i> and the edema toxin (ET) of <i>Bacillus anthracis</i> are both calmodulin-activated toxins with adenylyl cyclase activity that invade host cells and massively increase the cellular concentrations of a key second messenger molecule, 3&#8217;,5&#8217;-cyclic adenosine monophosphate (cAMP). However, the two toxins differ in the kinetics and mode of cell entry and generate different cAMP concentration gradients within the cell. While CyaA rapidly penetrates cells directly across their plasma membrane, the cellular entry of ET depends on receptor-mediated endocytosis and translocation of the enzymatic subunit across the endosomal membrane. We show that CyaA-generated membrane-proximal cAMP gradient strongly inhibits the activation and phosphorylation of Syk, Vav, and Pyk2, thus inhibiting opsonophagocytosis. By contrast, at similar overall cellular cAMP levels, the ET-generated perinuclear cAMP gradient poorly inhibits the activation and phosphorylation of these signaling proteins. Hence, differences in spatiotemporal distribution of cAMP produced by the two adenylyl cyclase toxins differentially affect the opsonophagocytic signaling in myeloid phagocytes.
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spelling doaj.art-01e3975f944d4cf9b0ebbe3885fd62132022-12-22T03:59:55ZengMDPI AGToxins2072-66512019-06-0111636210.3390/toxins11060362toxins11060362Distinct Spatiotemporal Distribution of Bacterial Toxin-Produced Cellular cAMP Differentially Inhibits Opsonophagocytic SignalingShakir Hasan0Waheed Ur Rahman1Peter Sebo2Radim Osicka3Institute of Microbiology of the CAS, v. v. i., Videnska 1083, 142 20 Prague, Czech RepublicInstitute of Microbiology of the CAS, v. v. i., Videnska 1083, 142 20 Prague, Czech RepublicInstitute of Microbiology of the CAS, v. v. i., Videnska 1083, 142 20 Prague, Czech RepublicInstitute of Microbiology of the CAS, v. v. i., Videnska 1083, 142 20 Prague, Czech RepublicMyeloid phagocytes have evolved to rapidly recognize invading pathogens and clear them through opsonophagocytic killing. The adenylate cyclase toxin (CyaA) of <i>Bordetella pertussis</i> and the edema toxin (ET) of <i>Bacillus anthracis</i> are both calmodulin-activated toxins with adenylyl cyclase activity that invade host cells and massively increase the cellular concentrations of a key second messenger molecule, 3&#8217;,5&#8217;-cyclic adenosine monophosphate (cAMP). However, the two toxins differ in the kinetics and mode of cell entry and generate different cAMP concentration gradients within the cell. While CyaA rapidly penetrates cells directly across their plasma membrane, the cellular entry of ET depends on receptor-mediated endocytosis and translocation of the enzymatic subunit across the endosomal membrane. We show that CyaA-generated membrane-proximal cAMP gradient strongly inhibits the activation and phosphorylation of Syk, Vav, and Pyk2, thus inhibiting opsonophagocytosis. By contrast, at similar overall cellular cAMP levels, the ET-generated perinuclear cAMP gradient poorly inhibits the activation and phosphorylation of these signaling proteins. Hence, differences in spatiotemporal distribution of cAMP produced by the two adenylyl cyclase toxins differentially affect the opsonophagocytic signaling in myeloid phagocytes.https://www.mdpi.com/2072-6651/11/6/3623′,5′-cyclic adenosine monophosphate (cAMP)adenylate cyclase toxinedema toxinopsonophagocytosisphagocytesSykVavPyk2signaling pathway
spellingShingle Shakir Hasan
Waheed Ur Rahman
Peter Sebo
Radim Osicka
Distinct Spatiotemporal Distribution of Bacterial Toxin-Produced Cellular cAMP Differentially Inhibits Opsonophagocytic Signaling
Toxins
3′,5′-cyclic adenosine monophosphate (cAMP)
adenylate cyclase toxin
edema toxin
opsonophagocytosis
phagocytes
Syk
Vav
Pyk2
signaling pathway
title Distinct Spatiotemporal Distribution of Bacterial Toxin-Produced Cellular cAMP Differentially Inhibits Opsonophagocytic Signaling
title_full Distinct Spatiotemporal Distribution of Bacterial Toxin-Produced Cellular cAMP Differentially Inhibits Opsonophagocytic Signaling
title_fullStr Distinct Spatiotemporal Distribution of Bacterial Toxin-Produced Cellular cAMP Differentially Inhibits Opsonophagocytic Signaling
title_full_unstemmed Distinct Spatiotemporal Distribution of Bacterial Toxin-Produced Cellular cAMP Differentially Inhibits Opsonophagocytic Signaling
title_short Distinct Spatiotemporal Distribution of Bacterial Toxin-Produced Cellular cAMP Differentially Inhibits Opsonophagocytic Signaling
title_sort distinct spatiotemporal distribution of bacterial toxin produced cellular camp differentially inhibits opsonophagocytic signaling
topic 3′,5′-cyclic adenosine monophosphate (cAMP)
adenylate cyclase toxin
edema toxin
opsonophagocytosis
phagocytes
Syk
Vav
Pyk2
signaling pathway
url https://www.mdpi.com/2072-6651/11/6/362
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AT petersebo distinctspatiotemporaldistributionofbacterialtoxinproducedcellularcampdifferentiallyinhibitsopsonophagocyticsignaling
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