Lethal and Edema Toxins in the Pathogenesis of Bacillus anthracis Septic Shock
- 1 February 2007
- journal article
- review article
- Published by American Thoracic Society in American Journal of Respiratory and Critical Care Medicine
- Vol. 175 (3) , 211-221
- https://doi.org/10.1164/rccm.200608-1239cp
Abstract
Recent research regarding the structure and function of Bacillus anthracis lethal (LeTx) and edema (ETx) toxins provides growing insights into the pathophysiology and treatment of shock with this lethal bacteria. These are both binary-type toxins composed of protective antigen necessary for their cellular uptake and either lethal or edema factors, the toxigenic moieties. The primary cellular receptors for protective antigen have been identified and constructed and key steps in the extracellular processing and internalization of the toxins clarified. Consistent with the lethal factor's primary action as an intracellular endopeptidase targeting mitogen-activated protein kinase kinases, growing evidence indicates that shock with this toxin does not result from an excessive inflammatory response. In fact, the potent immunosuppressive effects of LeTx may actually contribute to the establishment and persistence of infection. Instead, shock with LeTx may be related to the direct injurious effects of lethal factor on endothelial cell function. Despite the importance of LeTx, very recent studies show that edema factor, a potent adenyl cyclase, has the ability to make a substantial contribution to shock caused by B. anthracis and works additively with LeTx. Furthermore, ETx may contribute to the immunosuppressive effects of LeTx. Therapies under development that target several different steps in the cellular uptake and function of these two toxins have been effective in in vitro and in vivo systems. Understanding how best to apply these agents clinically and how they interact with conventional treatments should be goals for future research.Keywords
This publication has 95 references indexed in Scilit:
- Sepsis and Pathophysiology of Anthrax in a Nonhuman Primate ModelThe American Journal of Pathology, 2006
- Efficient Neutralization of Anthrax Toxin by Chimpanzee Monoclonal Antibodies against Protective AntigenThe Journal of Infectious Diseases, 2006
- Bacillus anthracisEdema Toxin InhibitsStaphylococcus aureusEnterotoxin B Effects In Vitro: a Potential Protein Therapeutic?Infection and Immunity, 2005
- Lethality during continuous anthrax lethal toxin infusion is associated with circulatory shock but not inflammatory cytokine or nitric oxide release in ratsAmerican Journal of Physiology-Regulatory, Integrative and Comparative Physiology, 2004
- Human antibodies from immunized donors are protective against anthrax toxin in vivoNature Biotechnology, 2003
- Calcium Dependence of the Interaction between Calmodulin and Anthrax Edema FactorJournal of Biological Chemistry, 2003
- A Dominant Negative Mutant of Bacillus anthracisProtective Antigen Inhibits Anthrax Toxin Action in VivoJournal of Biological Chemistry, 2001
- Dominant-Negative Mutants of a Toxin Subunit: An Approach to Therapy of AnthraxScience, 2001
- Anthrax lethal factor cleaves MKK3 in macrophages and inhibits the LPS/IFNγ‐induced release of NO and TNFαFEBS Letters, 1999
- Purification of Factor I and Recognition of a Third Factor of the Anthrax ToxinMicrobiology, 1961