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Open AccessJournal ArticleDOI

Anthrax toxin edema factor: a bacterial adenylate cyclase that increases cyclic AMP concentrations of eukaryotic cells.

Stephen H. Leppla
- 01 May 1982 - 
- Vol. 79, Iss: 10, pp 3162-3166
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TLDR
It is shown here that EF is an adenylate cyclase [ATP pyrophosphate-lyase (cyclizing), EC 4.6.1] produced by Bacillus anthracis in an inactive form and nearly equals that of the most active known cyclase.
Abstract: 
Anthrax toxin is composed of three proteins: protective antigen (PA), lethal factor (LF), and edema factor (EF). These proteins individually cause no known physiological effects in animals but in pairs produce two toxic actions. Injection of PA with LF causes death of rats in 60 min, whereas PA with EF causes edema in the skin of rabbits and guinea pigs. The mechanisms of action of these proteins have not been determined. It is shown here that EF is an adenylate cyclase [ATP pyrophosphate-lyase (cyclizing), EC 4.6.1.1] produced by Bacillus anthracis in an inactive form. Activation occurs upon contact with a heat-stable eukaryotic cell material. The specific activity of the resulting adenylate cyclase nearly equals that of the most active known cyclase. In Chinese hamster ovary cells exposed to PA and EF, cAMP concentrations increase without a lag to values about 200-fold above normal, remain high in the continued presence of toxin, and decrease rapidly after its removal. The increase in cAMP is completely blocked by excess LF. It is suggested that PA interacts with cells to form a receptor system by which EF and perhaps LF gain access to the cytoplasm.

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Citations
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Journal ArticleDOI

Purification and characterization of Clostridium perfringens iota toxin: dependence on two nonlinked proteins for biological activity.

B G Stiles, +1 more
- 01 Dec 1986 - 
TL;DR: These results demonstrated that C. perfringens iota toxin required two different, nonlinked protein components for biological activity, and demonstrated that the biological activity of ia was heat stable, whereas ib was inactivated at 55 degrees C.
Journal ArticleDOI

Proteolytic activation of bacterial toxins: role of bacterial and host cell proteases.

TL;DR: Proteolysis was found to have a different role in several binary toxins, in which cleavage within a specific sequence exposes binding sites or surfaces by which several toxin proteins associate.
Journal ArticleDOI

Dendritic Cells Endocytose Bacillus anthracis Spores: Implications for Anthrax Pathogenesis

TL;DR: It is found that human DCs readily engulfed fully pathogenic Ames and attenuated B. anthracis spores predominately by coiling phagocytosis, suggesting that B. Anthracis may exploit DCs to facilitate infection.
Journal ArticleDOI

Anthrax edema toxin differentially regulates lipopolysaccharide-induced monocyte production of tumor necrosis factor alpha and interleukin-6 by increasing intracellular cyclic AMP.

TL;DR: The disruption of cytokine networks as a consequence of unregulated, ET-induced cAMP accumulation in human monocytes may impair cellular antimicrobial responses and contribute to clinical signs and symptoms.
Journal ArticleDOI

Role of toxin functional domains in anthrax pathogenesis.

TL;DR: Investigation of the role of the functional domains of anthrax toxins during infection found that the binding of LF to PA in vivo was necessary and sufficient for a strong antibody response against LF, whereas neither LF activity nor binding of lethal toxin complex to the cell surface was required.
References
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Journal Article

Protein Measurement with the Folin Phenol Reagent

TL;DR: Procedures are described for measuring protein in solution or after precipitation with acids or other agents, and for the determination of as little as 0.2 gamma of protein.
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Restoration of Several Morphological Characteristics of Normal Fibroblasts in Sarcoma Cells Treated with Adenosine-3':5'-Cyclic Monophosphate and Its Derivatives

TL;DR: The data suggest that cyclic AMP may be an important factor in the determination of morphology of normal fibroblasts and this function may be lost or altered during transformation.
Journal ArticleDOI

Activation of adenylate cyclase by choleragen.

J Moss, +1 more
- 01 Jan 1979 - 
TL;DR: An attempt is made to evaluate the mechanism of action of NAD Glycohydrolase and ADP-Ribosyltransferase on GTP-Binding Protein and GTPase Activity in response to the presence of Gangliosides and Their Oligosaccharides in Choleragen.
Journal ArticleDOI

A Permeability Factor (Toxin) found in Cholera Stools and Culture Filtrates and its Neutralization by Convalescent Cholera Sera.

TL;DR: A Permeability Factor (Toxin) found in Cholera Stools and Culture Filtrates and its Neutralization by Convalescent CholERA Sera is found to be neutralized by convalescent cholera patients.
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