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 essential–delay 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

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 April 15, 2009