Introduction
Lethal Factor (LF) is one of the enzyme components belonging to the Anthrax Toxin . Anthrax toxin is a three protein exotoxin secreted by the bacterium Bacillus anthracis made up of a binding protein known as the protective antigen (PA) and two enzyme components known as edema factor (EF) and lethal factor (LF).
Human Interaction
Anthrax is primarily a disease of domesticated and wild animals. Herbivores, such as cattle, sheep, horses, mules and goats are primarily affected because these animals maybe grazing on soils contaminated with Bacillus anthracis endospores.[1][2] The blood of an animal that dies of anthrax can contain upward of 109 vegetative bacteria per milliliter. As the carcass decays, the bacteria form highly infectious endospores, which contaminate the local environment and can remain viable for long time periods. [1] The endosopres produced by Bacillus Anthracis remains viable for lengthy periods do to the
poly-D- glutamic acid capsule, which itself is nontoxic. This capsule functions to protect the endospore from complement and other bactericidal components found in serum against phagocytic engulfment and destruction. This capsule plays an important role during the infection of anthrax, but is not important during the disease phase, which is primarily caused by PA, EF, LF. Genes encoding this plasmid are located on plasmid pX02.[1][3].
Anthrax is not common is for humans. Humans become infect by be exposed to farm animal s or contaminated animal products such as wool, hides, flesh and blood. There are three ways in which Anthrax can be transmitted to humans:
Cutaneous Anthrax which is the most common form of the disease. This usually occurs when the endospores enter the body through injured skin and germinate. In most cases the bacteria remain contain at the site of infection and present as a lesion. A main characteristic of this type of infection is gelatinous edema at the site infection. As the infection advances, the site of infection goes through multiple stages. Next a papule (solid elevation of the skin) develops which turns into a vesicle (a small fluid-filled blister). The vesicle then develops into a pustule (pus-filled blister). The finally stage is the formation of a necrotic ulcer. In rare case, the infection could spread to the blood stream and cause septicemia. Treatment is often not needed.
Gastrointestinal Anthrax occurs through the ingestion of spores-contaminated meat. The spores then invade the mucosa through a preexisting lesion. After germination, spores spread from the mucosal lesion into the lymphatic system. The form of Anthrax is associated with a high mortality rate but is considered the rarest of the three types of infection.
Inhalation Anthrax is the most fatal of the three infections. Also know as woolsorters' disease, this form involves the inhalation of spore usually contained in animal hair and hides. The spores colonize the Alveolar macrophages and it is believed the believed the macrophages serve both as the sites of germination and as vehicles for transporting the bacteria. At this point the bacteria can rapidly spread throughout the body. If left untreated death is certain. Even with antibiotics mortality rates are high.
Treatments
Antibiotics are used to treat Cutaneous and Inhalation Anthrax infections. The primary antibiotics used are Ciprofloxacin and Doxycycline. Antibiotics should to be administered before symptoms arise, which will likely decrease the fatality rate. If administered after symptoms arise, there is a high chance of fatality. The duration of treatment is 60 days of antibiotics to ensure all spores have germinated. In so cases more than two antibiotics are administered. If systemic spread is seen, this reduces survival rate.
Structure
Function
References
