Cellular Activities of Bacillus Anthracis

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Bacillus anthracis is a gram positive rod bacteria which can cause a serious, and more often than not, lethal disease known simply as anthrax. Anthrax received a substantial amount of attention in 2001, when it was feared the bacteria would be used as a form of biological warfare. The situation was resolved, but not before 5 people were declared dead and another 17 injured in the space of several weeks. This led to an increase in the study of Bacillus anthracis, and although multiple discoveries have been made concerning methods of infection, there are still more questions to be answered.
Bacillus anthracis is highly virulent, a factor that can be largely attributed to its ability to form endospores, and its secretion of a substance known as anthrax toxin. Endospores are non-reproductive structures that are highly resistant to most processes that could kill a cell, such as extreme heat or radiation, and they form under circumstances of starvation as a way of preserving the toxin. Anthrax toxin itself is made of three components which are only lethal when combined. The three toxins are protective antigen, lethal factor, and edema factor; hereafter referred to as PA, LF, and EF respectively. LF is a Zn²⁺ dependent protease, and EF is a calmodulin-dependent adenylyl cyclase. 1
As a general summary, the anthrax toxin infects the host cell by creating a pore in the plasma membrane and causing the cell to intake LF/EF via receptor mediated endocytosis. LF and EF then create another pore to leave the endosome before it gets to its destination, releasing it into the cytosol before it is properly detected.
This infection begins as PA binds to surface receptors on the target host cell. It is necessary for infection for multiple PA toxin...

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...membrane, simulating the gradient across the endosomal membrane, such that the cis compartment is acidic and the trans compartment neutral, acidic side chains approaching the barrier from the cis direction will have a higher probability of being protonated and diffusing past the barrier. Thus thermal fluctuations of the polypeptide chain will be biased in the cis-to-trans direction, causing...a net translocation in that direction. Also, protons that become associated with acidic side chains in the cis compartment are released into the trans compartment, making the PA pore formally a protein–proton symporter

This mechanism for the active transport of LF and EF across the endosomal membrane is well supported, but is still under scrutiny.
Another largely unknown mechanism is how the two toxins are refolded once in the cytoplasm, and what they actually do from there.

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