|
Anthrax is an acute infectious
disease caused by the spore-forming bacterium Bacillus
anthracis. Anthrax most commonly occurs in hoofed mammals
and can also infect humans.
Symptoms of disease vary depending on how the disease
was contracted, but usually occur within 7 days after
exposure. The serious forms of human anthrax are inhalation
anthrax, cutaneous anthrax, and intestinal anthrax.
Initial symptoms of inhalation anthrax infection may
resemble a common cold. After several days, the symptoms
may progress to severe breathing problems and shock.
Inhalation anthrax is often fatal. |
 |
|
|
|
|
|
The intestinal disease form of anthrax may follow the consumption
of contaminated food and is characterized by an acute inflammation
of the intestinal tract. Initial signs of nausea, loss of
appetite, vomiting, and fever are followed by abdominal
pain, vomiting of blood, and severe diarrhea.
Direct person-to-person spread of anthrax is extremely
unlikely, if it occurs at all. Therefore, there is no need
to immunize or treat contacts of persons ill with anthrax,
such as household contacts, friends, or coworkers, unless
they also were also exposed to the same source of infection.
In persons exposed to anthrax, infection can be prevented
with antibiotic treatment.
However, bioterrorists may "weaponize" or mutate anthrax to be resistant to known antibiotics (antibiotics are drugs that kill bacteria). It is because of this weaponization that it is critical to have a steady stream of new drugs and targets in the pipeline. During weaponization, the known antibiotic is actually used to "evolve" anthrax and strains are selected that are resistant to the antibiotic. During the Gulf War, the U.S. Government had troups carry Cipro because it was the newest antibiotic available and the Iraqis would not have had time to weaponize anthrax against it.
For the latest public terrorist attack, Cipro was again chosen, but in this case the anthrax strains used might have already been weaponized to resist Cipro.
Early antibiotic treatment of anthrax is essentialdelay
lessens chances for survival. Anthrax usually is susceptible
to penicillin, doxycycline, and fluoroquinolones.
An anthrax vaccine also can prevent infection. Vaccination
against anthrax is not recommended for the general public
to prevent disease and is not available.
|
|
|
|
| TARGET - Anthrax Lethal Factor |
|
|
|
|
(D2OL)'s first target was the Anthrax Lethal Factor
protein. Lethal Factor's structure was recently published
in the prestigious journal Nature www.nature.com. Download
the software now to contribute to the effort.
Unlike other bacterial pathogens, the Anthrax bacteria
produces a toxin fatal to humans, the Anthrax Lethal
Factor. The Drug Design Optimization Lab is focused
on the discovery of antitoxins capable of neutralizing
the toxin after exposure has occured.
D2OL) is screening real potential drug candidates
against the structure of Anthrax Lethal Factor with
your help. We appreciate your help in recruiting volunteers
for this project and contributing to the lead generation
process for this deadly scourge. Please keep in mind,
credible "hits" represent chemical compounds
that exist today and can be tested in live laboratories.
|

Figure A represents the Anthrax Lethal Factor structure, click on it to see details (graphic).
|
|
|
|
|
|
Crystal Structure of the Anthrax Lethal Factor
Andrew D. Pannifer1, Thiang Yian Wong2, Robert Schwarzenbacher2, Martin Renatus2, Carlo Petosa1,
Jadwiga Bienkowska3, D. Borden Lacy4, R. John Collier4, Sukjoon Park5, Stephen H. Leppala5,
Phillip Hanna6 & Robert C. Liddington1
1Biochemistry Department, University of Leicester, Leicester LE1 7RH, UK
2The Burnhma Institute, 10901 North Torry Pines Road, La Jolla, California 92037, USA
3Dana Farber Cancer Institute, Boston, Massachusettes 02115, USA
4Department of Microbiology and Molecular Genetics, Havard Medical School, 200 Longwood Avenue, Boston, Massachusetts 02115, USA
5National Institute of Dental and Craniofacial Research, National Institutes of Health, 9000 Rockville Pike, Bethesda, Maryland 20892, USA
6Department of Microbiology and Immunology, University of Michigan Medical School, 5641 Medical Science II, Ann Arbor, Michigan 48109, USA
We would like to thank the authors for supplying the crystal structures to our laboratories
prior to public release.
this page last
reviewed October 1, 2004
|
|
|
|
|