Abstract
Anthrax toxin is composed of 3 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 2 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 pyrophosphatase-lyase (cyclizing), EC 4.6.1.1] produced by B. 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. Evidently, PA interacts with cells to form a receptor system by which EF and perhaps LF gain access to the cytoplasm.