4.6 Article

Cholesterol stimulates the lytic activity of Adenylate Cyclase Toxin on lipid membranes by promoting toxin oligomerization and formation of pores with a greater effective size

Journal

FEBS JOURNAL
Volume 288, Issue 23, Pages 6795-6814

Publisher

WILEY
DOI: 10.1111/febs.16107

Keywords

adenylate cyclase; bacterial toxins; lipid-protein interactions; pore-forming proteins

Funding

  1. Spanish Ministerio de Economia y Competitividad [BFU2017-82758-P]
  2. Basque Government [IT1264-19]
  3. Bizkaia Biophysics Foundation
  4. Basque Government

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Several toxins interact with cholesterol in different ways, affecting cellular permeabilization. Cholesterol enhances the lytic potency of ACT by promoting toxin oligomerization, a crucial step for membrane permeabilization. The mechanistic details by which cholesterol facilitates lytic pore formation remain largely unexplored.
Several toxins acting on animal cells present different, but specific, interactions with cholesterol. Bordetella pertussis infects the human respiratory tract and causes whooping cough, a highly contagious and resurgent disease. Its virulence factor adenylate cyclase toxin (ACT) plays an important role in the course of infection. ACT is a pore-forming cytolysin belonging to the Repeats in ToXin (RTX) family of leukotoxins/hemolysins and is capable of permeabilizing several cell types and lipid vesicles. Previously, we observed that in the presence of cholesterol ACT induces greater liposome permeabilization. Similarly, recent reports also implicate cholesterol in the cytotoxicity of an increasing number of pore-forming RTX toxins. However, the mechanistic details by which this sterol promotes the lytic activity of ACT or of these other RTX toxins remain largely unexplored and poorly understood. Here, we have applied a combination of biophysical techniques to dissect the role of cholesterol in pore formation by ACT. Our results indicate that cholesterol enhances the lytic potency of ACT by promoting toxin oligomerization, a step which is indispensable for ACT to accomplish membrane permeabilization and cell lysis. Since our experimental design eliminates the possibility that this cholesterol effect derives from toxin accumulation due to lateral lipid phase segregation, we hypothesize that cholesterol facilitates lytic pore formation, by favoring a toxin conformation more prone to protein-protein interactions and oligomerization. Our data shed light on the complex relationship between lipid membranes and protein toxins acting on these membranes. Coupling cholesterol binding, increased oligomerization and increased lytic activity is likely pertinent for other RTX cytolysins.

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