Cyclic AMP-Elevating Capacity of Adenylate Cyclase Toxin-Hemolysin Is Sufficient for Lung Infection but Not for Full Virulence of Bordetella pertussis

Author:

Skopova Karolina1,Tomalova Barbora1,Kanchev Ivan2,Rossmann Pavel1,Svedova Martina1,Adkins Irena1,Bibova Ilona1,Tomala Jakub1,Masin Jiri1,Guiso Nicole34,Osicka Radim1,Sedlacek Radislav2,Kovar Marek1,Sebo Peter1

Affiliation:

1. Institute of Microbiology of the CAS, v.v.i., Prague, Czech Republic

2. Czech Centre for Phenogenomics, Division BIOCEV, Institute of Molecular Genetics of the CAS, v.v.i., Czech Academy of Sciences, Prague, Czech Republic

3. Institut Pasteur, Molecular Prevention and Therapy of Human Diseases Unit, Paris, France

4. Centre National de la Recherche Scientifique (CNRS), URA3012, Paris, France

Abstract

ABSTRACT The adenylate cyclase toxin-hemolysin (CyaA, ACT, or AC-Hly) of Bordetella pertussis targets phagocytic cells expressing the complement receptor 3 (CR3, Mac-1, α M β 2 integrin, or CD11b/CD18). CyaA delivers into cells an N-terminal adenylyl cyclase (AC) enzyme domain that is activated by cytosolic calmodulin and catalyzes unregulated conversion of cellular ATP into cyclic AMP (cAMP), a key second messenger subverting bactericidal activities of phagocytes. In parallel, the hemolysin (Hly) moiety of CyaA forms cation-selective hemolytic pores that permeabilize target cell membranes. We constructed the first B. pertussis mutant secreting a CyaA toxin having an intact capacity to deliver the AC enzyme into CD11b-expressing (CD11b + ) host phagocytes but impaired in formation of cell-permeabilizing pores and defective in cAMP elevation in CD11b cells. The nonhemolytic AC + Hly bacteria inhibited the antigen-presenting capacities of coincubated mouse dendritic cells in vitro and skewed their Toll-like receptor (TLR)-triggered maturation toward a tolerogenic phenotype. The AC + Hly mutant also infected mouse lungs as efficiently as the parental AC + Hly + strain. Hence, elevation of cAMP in CD11b cells and/or the pore-forming capacity of CyaA were not required for infection of mouse airways. The latter activities were, however, involved in bacterial penetration across the epithelial layer, enhanced neutrophil influx into lung parenchyma during sublethal infections, and the exacerbated lung pathology and lethality of B. pertussis infections at higher inoculation doses (>10 7 CFU/mouse). The pore-forming activity of CyaA further synergized with the cAMP-elevating activity in downregulation of major histocompatibility complex class II (MHC-II) molecules on infiltrating myeloid cells, likely contributing to immune subversion of host defenses by the whooping cough agent.

Funder

Agency for Health Research

Czech Science Foundation

Institutional Research Project of the Institute of Microbiology

Institutional Funding of Institut Pasteur and CNRS

Czech National Node to EATRIS project

Myes of the CR

AZV project

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

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