Blockade of the Adenylate Cyclase Toxin Synergizes with Opsonizing Antibodies to Protect Mice against Bordetella pertussis

ABSTRACT Bordetella produces an array of virulence factors, including the adenylate cyclase toxin (ACT), which is essential, immunogenic in humans, and highly conserved. Despite mediating immune-evasive functions as a leukotoxin, ACT’s potential role as a protective antigen is unclear. To better und...

Full description

Bibliographic Details
Main Authors: Andrea M. DiVenere, Dzifa Amengor, Rui P. Silva, Jory A. Goldsmith, Jason S. McLellan, Jennifer A. Maynard
Format: Article
Language:English
Published: American Society for Microbiology 2022-08-01
Series:mBio
Subjects:
Online Access:https://journals.asm.org/doi/10.1128/mbio.01527-22
_version_ 1818473355653677056
author Andrea M. DiVenere
Dzifa Amengor
Rui P. Silva
Jory A. Goldsmith
Jason S. McLellan
Jennifer A. Maynard
author_facet Andrea M. DiVenere
Dzifa Amengor
Rui P. Silva
Jory A. Goldsmith
Jason S. McLellan
Jennifer A. Maynard
author_sort Andrea M. DiVenere
collection DOAJ
description ABSTRACT Bordetella produces an array of virulence factors, including the adenylate cyclase toxin (ACT), which is essential, immunogenic in humans, and highly conserved. Despite mediating immune-evasive functions as a leukotoxin, ACT’s potential role as a protective antigen is unclear. To better understand the contributions of humoral anti-ACT immunity, we evaluated protection against Bordetella pertussis by antibodies binding structurally defined ACT epitopes in a mouse pneumonia model. An ACT-neutralizing antibody, but not a nonneutralizing antibody or an isotype control, significantly increased mouse survival after lethal challenge with B. pertussis. When modified to impair Fc effector functions, the neutralizing antibody retained protective capabilities, indicating that protection was mediated by the blockade of the interactions of ACT with its αMβ2 integrin receptor. After infection with a lower bacterial dose, ACT neutralization synergistically reduced lung bacterial colonization levels when combined with an opsonic antibody binding the surface antigen pertactin. Notably, protection was significantly enhanced when antibodies were administered intranasally as opposed to systemically, indicating that local immune responses are key to antibody-mediated protection against ACT and pertactin. These data reconcile previous conflicting reports to indicate that neutralizing anti-ACT antibodies support the phagocytosis of opsonized B. pertussis and thereby contribute to pertussis protection in vivo. IMPORTANCE Despite high vaccine coverage in developed countries, the incidence of pertussis has increased in recent decades, often leading to severe consequences for sensitive groups, including infants. For this reason, improving the efficacy of pertussis vaccines is critical, and the addition of new antigens is a leading strategy to achieve this goal. The Bordetella pertussis adenylate cyclase toxin (ACT) acts to disarm host immunity and is considered a promising vaccine candidate since it is found in all Bordetella species. In this work, we show that antibodies neutralizing ACT offer protection against pertussis. Using a murine infection model, we show that antibodies neutralizing ACT can contribute to protection against infection through synergistic interactions with antibodies recognizing current vaccine antigens. Our data can help guide the design of future vaccines, whereby the inclusion of ACT-based immunogens might increase protection against pertussis infection.
first_indexed 2024-04-14T04:21:43Z
format Article
id doaj.art-362d14f34aae418bae944b32e8cf4808
institution Directory Open Access Journal
issn 2150-7511
language English
last_indexed 2024-04-14T04:21:43Z
publishDate 2022-08-01
publisher American Society for Microbiology
record_format Article
series mBio
spelling doaj.art-362d14f34aae418bae944b32e8cf48082022-12-22T02:12:28ZengAmerican Society for MicrobiologymBio2150-75112022-08-0113410.1128/mbio.01527-22Blockade of the Adenylate Cyclase Toxin Synergizes with Opsonizing Antibodies to Protect Mice against Bordetella pertussisAndrea M. DiVenere0Dzifa Amengor1Rui P. Silva2Jory A. Goldsmith3Jason S. McLellan4Jennifer A. Maynard5Department of Chemical Engineering, University of Texas, Austin, Texas, USADepartment of Molecular Biosciences, University of Texas, Austin, Texas, USADepartment of Molecular Biosciences, University of Texas, Austin, Texas, USADepartment of Molecular Biosciences, University of Texas, Austin, Texas, USADepartment of Molecular Biosciences, University of Texas, Austin, Texas, USADepartment of Chemical Engineering, University of Texas, Austin, Texas, USAABSTRACT Bordetella produces an array of virulence factors, including the adenylate cyclase toxin (ACT), which is essential, immunogenic in humans, and highly conserved. Despite mediating immune-evasive functions as a leukotoxin, ACT’s potential role as a protective antigen is unclear. To better understand the contributions of humoral anti-ACT immunity, we evaluated protection against Bordetella pertussis by antibodies binding structurally defined ACT epitopes in a mouse pneumonia model. An ACT-neutralizing antibody, but not a nonneutralizing antibody or an isotype control, significantly increased mouse survival after lethal challenge with B. pertussis. When modified to impair Fc effector functions, the neutralizing antibody retained protective capabilities, indicating that protection was mediated by the blockade of the interactions of ACT with its αMβ2 integrin receptor. After infection with a lower bacterial dose, ACT neutralization synergistically reduced lung bacterial colonization levels when combined with an opsonic antibody binding the surface antigen pertactin. Notably, protection was significantly enhanced when antibodies were administered intranasally as opposed to systemically, indicating that local immune responses are key to antibody-mediated protection against ACT and pertactin. These data reconcile previous conflicting reports to indicate that neutralizing anti-ACT antibodies support the phagocytosis of opsonized B. pertussis and thereby contribute to pertussis protection in vivo. IMPORTANCE Despite high vaccine coverage in developed countries, the incidence of pertussis has increased in recent decades, often leading to severe consequences for sensitive groups, including infants. For this reason, improving the efficacy of pertussis vaccines is critical, and the addition of new antigens is a leading strategy to achieve this goal. The Bordetella pertussis adenylate cyclase toxin (ACT) acts to disarm host immunity and is considered a promising vaccine candidate since it is found in all Bordetella species. In this work, we show that antibodies neutralizing ACT offer protection against pertussis. Using a murine infection model, we show that antibodies neutralizing ACT can contribute to protection against infection through synergistic interactions with antibodies recognizing current vaccine antigens. Our data can help guide the design of future vaccines, whereby the inclusion of ACT-based immunogens might increase protection against pertussis infection.https://journals.asm.org/doi/10.1128/mbio.01527-22immune evasionneutralizing antibodiespediatric infectious diseasepertussis toxins
spellingShingle Andrea M. DiVenere
Dzifa Amengor
Rui P. Silva
Jory A. Goldsmith
Jason S. McLellan
Jennifer A. Maynard
Blockade of the Adenylate Cyclase Toxin Synergizes with Opsonizing Antibodies to Protect Mice against Bordetella pertussis
mBio
immune evasion
neutralizing antibodies
pediatric infectious disease
pertussis toxins
title Blockade of the Adenylate Cyclase Toxin Synergizes with Opsonizing Antibodies to Protect Mice against Bordetella pertussis
title_full Blockade of the Adenylate Cyclase Toxin Synergizes with Opsonizing Antibodies to Protect Mice against Bordetella pertussis
title_fullStr Blockade of the Adenylate Cyclase Toxin Synergizes with Opsonizing Antibodies to Protect Mice against Bordetella pertussis
title_full_unstemmed Blockade of the Adenylate Cyclase Toxin Synergizes with Opsonizing Antibodies to Protect Mice against Bordetella pertussis
title_short Blockade of the Adenylate Cyclase Toxin Synergizes with Opsonizing Antibodies to Protect Mice against Bordetella pertussis
title_sort blockade of the adenylate cyclase toxin synergizes with opsonizing antibodies to protect mice against bordetella pertussis
topic immune evasion
neutralizing antibodies
pediatric infectious disease
pertussis toxins
url https://journals.asm.org/doi/10.1128/mbio.01527-22
work_keys_str_mv AT andreamdivenere blockadeoftheadenylatecyclasetoxinsynergizeswithopsonizingantibodiestoprotectmiceagainstbordetellapertussis
AT dzifaamengor blockadeoftheadenylatecyclasetoxinsynergizeswithopsonizingantibodiestoprotectmiceagainstbordetellapertussis
AT ruipsilva blockadeoftheadenylatecyclasetoxinsynergizeswithopsonizingantibodiestoprotectmiceagainstbordetellapertussis
AT joryagoldsmith blockadeoftheadenylatecyclasetoxinsynergizeswithopsonizingantibodiestoprotectmiceagainstbordetellapertussis
AT jasonsmclellan blockadeoftheadenylatecyclasetoxinsynergizeswithopsonizingantibodiestoprotectmiceagainstbordetellapertussis
AT jenniferamaynard blockadeoftheadenylatecyclasetoxinsynergizeswithopsonizingantibodiestoprotectmiceagainstbordetellapertussis