Role of Major Toxin Virulence Factors in Pertussis Infection and Disease Pathogenesis
- PMID: 31376138
- PMCID: PMC7038575
- DOI: 10.1007/5584_2019_403
Role of Major Toxin Virulence Factors in Pertussis Infection and Disease Pathogenesis
Abstract
Bordetella pertussis produces several toxins that affect host-pathogen interactions. Of these, the major toxins that contribute to pertussis infection and disease are pertussis toxin, adenylate cyclase toxin-hemolysin and tracheal cytotoxin. Pertussis toxin is a multi-subunit protein toxin that inhibits host G protein-coupled receptor signaling, causing a wide array of effects on the host. Adenylate cyclase toxin-hemolysin is a single polypeptide, containing an adenylate cyclase enzymatic domain coupled to a hemolysin domain, that primarily targets phagocytic cells to inhibit their antibacterial activities. Tracheal cytotoxin is a fragment of peptidoglycan released by B. pertussis that elicits damaging inflammatory responses in host cells. This chapter describes these three virulence factors of B. pertussis, summarizing background information and focusing on the role of each toxin in infection and disease pathogenesis, as well as their role in pertussis vaccination.
Keywords: Adenylate cyclase toxin-hemolysin; Bordetella toxins; Pertussis pathogenesis; Pertussis toxin; Tracheal Cytotoxin.
Figures
References
-
- Adamson PB, Hull SS Jr., Vanoli E, De Ferrari GM, Wisler P, Foreman RD, Watanabe AM, Schwartz PJ (1993) Pertussis toxin-induced ADP ribosylation of inhibitor G proteins alters vagal control of heart rate in vivo. The American journal of physiology 265 (2 Pt 2):H734–740 - PubMed
-
- Agarwal N, Lamichhane G, Gupta R, Nolan S, Bishai WR (2009) Cyclic AMP intoxication of macrophages by a Mycobacterium tuberculosis adenylate cyclase. Nature 460 (7251):98–102. - PubMed
-
- Ahmad JN, Cerny O, Linhartova I, Masin J, Osicka R, Sebo P (2016) cAMP signalling of Bordetella adenylate cyclase toxin through the SHP-1 phosphatase activates the BimEL-Bax pro-apoptotic cascade in phagocytes. Cell Microbiol 18 (3):384–398. - PubMed
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
