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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

Anthrax undervalued zoonosis

TL;DR: The atypicality of the phenomenon may lead health workers to misdiagnose and, consequently, an inappropriately manage of affected carcasses with a consequent and inevitable increase in the risk of human infection.
Journal ArticleDOI

The chymotrypsin-sensitive site, FFD315, in anthrax toxin protective antigen is required for translocation of lethal factor.

TL;DR: The results suggest that the chymotrypsin-sensitive site in PA is required for membrane channel formation and translocation of LF into the cytosol, and may be useful as a replacement for PA in anthrax vaccines.
Journal ArticleDOI

Functional analysis of Bacillus anthracis protective antigen by using neutralizing monoclonal antibodies.

TL;DR: There is an additive effect between the two MAbs against PA and a MAb against LF, in protecting mice against a lethal challenge by the Sterne strain, and this work contributes to the functional analysis of PA and offers immunotherapeutic perspectives for the treatment of anthrax disease.
Journal ArticleDOI

Targeting proteins to the cell wall of sporulating Bacillus anthracis.

TL;DR: It is shown here that sortase C (SrtC) cleaves the LPNTA sorting signal of BasH and BasI, thereby targeting both polypeptides to the cell wall of sporulating bacilli, and appears to display no defect during the initial stages of infection and precipitate lethal anthrax disease in guinea pigs at a similar rate as wild‐type B.
Journal ArticleDOI

Key tissue targets responsible for anthrax-toxin-induced lethality

TL;DR: Results show that lethality induced by LT and ET occurs through damage to distinct cell types; whereas targeting cardiomyocytes and vascular smooth muscle cells is required for LT-induced mortality, ET-induced lethality occurs mainly through its action in hepatocytes.
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.
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Activation of adenylate cyclase by choleragen.

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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.
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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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