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Updated: Mar 17, 2026

Evaluation of Host-Pathogen Responses and Vaccine Efficacy in Mice
Published on: February 22, 2019
Bordetella pertussis modulates human macrophage defense gene expression
Hugo Alberto Valdez1, Juan Marcos Oviedo1, Juan Pablo Gorgojo1
1CINDEFI (UNLP CONICET La Plata), Facultad de Ciencias Exactas, Universidad Nacional de La Plata, 1900 La Plata, Buenos Aires, Argentina.
Bordetella pertussis evades immune responses by suppressing macrophage bactericidal activity. Pertussis toxin and adenylate cyclase are key virulence factors enabling bacterial survival within host cells.
Area of Science:
- Immunology
- Microbiology
- Cell Biology
Background:
- Bordetella pertussis causes whooping cough and can persist within human macrophages.
- Understanding intracellular survival mechanisms is crucial for controlling pertussis outbreaks.
Purpose of the Study:
- To investigate the host cell response to B. pertussis infection in macrophages.
- To identify mechanisms of intracellular bacterial survival.
Main Methods:
- Used THP-1 cells differentiated into macrophages.
- Analyzed gene expression related to bactericidal and inflammatory responses.
- Assessed bacterial load and host cell viability over time.
Main Results:
- Macrophage bactericidal and inflammatory responses were downregulated post-infection.
- Intracellular B. pertussis replication increased over time.
- Pertussis toxin (Ptx) and adenylate cyclase (CyaA) are essential for manipulating host responses and intracellular survival.
Conclusions:
- B. pertussis manipulates host defense genes to establish intracellular infections.
- Toxins Ptx and CyaA are critical for B. pertussis persistence within macrophages.
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