Anthrax
Anthrax Introduction
Anthrax is described in the early literature of the Greeks, Romans, and Hindus. The fifth plague, described in the book of Genesis, may be among the earliest descriptions of anthrax.
Anthrax is caused by exposure to the spores of the bacteria Bacillus anthracis that become entrenched in the host body and produce lethal poisons. It is primarily a disease of grazing animals such as cattle, sheep, goats, and horses. Pigs are more resistant, as are dogs and cats. Birds usually are naturally resistant to anthrax. Buzzards and vultures are naturally resistant to anthrax but may transmit the spores on their talons and beaks.
The bacteria that cause anthrax are able to go into a dormant phase, in which they form spores. Spores can exist in the environment for decades. Under the right conditions, the dormant spores can germinate and multiply.
If terrorists were to use the anthrax spores, they would most likely want to disperse it into the air for mass effect. As was seen in October 2001, terrorists could also deliver anthrax by other means, such as placing spores in letters or packages to be opened and inhaled and handled by unsuspecting recipients.
People of any age may be affected. Most cases are mild and go away with treatment. Anthrax, however, can be lethal. There are several ways anthrax can cause illness. These are the 3 main ways anthrax affects humans:
- Cutaneous (skin) anthrax causes a characteristic sore on the skin and results from exposure to the spores after handling sick animals or contaminated animal wool, hair, hides, or bone meal products. It is an occupational hazard for veterinarians, farmers, and people who handle animal products. Where the bacteria are common, human infection remains uncommon. Humans are relatively resistant, but the spores may gain access through even tiny breaks in the skin. Cutaneous anthrax is easy to cure if it is treated early with appropriate antibiotics.
- Inhalational anthrax results from breathing anthrax spores into the lungs. People who handle animal hides infested with spores may develop inhalational anthrax, known as woolsorter's disease. Once inhaled, the organisms multiply and may spread their toxins to the bloodstream and many other organs. Infection may spread from the liver, spleen, and kidneys back into the bloodstream, thus causing an overwhelming infection and death. This type of infection (known as septicemic anthrax) most commonly follows inhalational anthrax.
- Gastrointestinal anthrax results from eating meat products that contain anthrax. Gastrointestinal anthrax is difficult to diagnose. It can produce sores in the mouth and throat. A person who has eaten contaminated products may feel throat pain or have difficulty swallowing. This form of anthrax has a very high death rate.
Anthrax Causes
Anthrax is caused by the bacteria B anthracis. These are rod-shaped germs that can change from "normal" bacteria into spores (or single-celled seeds that can reproduce the bacteria).
Anthrax Signs and Symptoms
- Cutaneous (skin) anthrax
- Cutaneous anthrax occurs 1-7 days (usually 2-5) after spores enter the body through breaks in the skin.
- This form most commonly affects the exposed areas of the arms and, to a lesser extent, the head and neck.
- The infection may spread throughout the body in up to 20% of untreated cases.
- Cutaneous anthrax begins as a small pimplelike lesion (a sore) that enlarges in 24-48 hours to form a "malignant pustule" at the site of the infection. This sore (about 2-3 cm or about an inch) is round with a raised edge. The sore is not painful. The central area of infection is surrounded by small blisters filled with bloody or clear fluid containing many bacteria. A black scab forms at the site of the sore in 7-10 days and lasts for 7-14 days before separating. The surrounding area may be swollen and painful and may last long after the scab forms.
- Sores that affect the neck may cause swelling that could affect breathing.
- Inhalational anthrax
- Inhalational anthrax begins abruptly, 1-60 days (usually 1-3 days) after inhaling large amounts of anthrax spores. The size of the spores is extremely important when it comes to causing disease, and this depends upon the techniques of the person producing the spores. Spores that are too small are inhaled but then immediately exhaled and do not remain in the lungs to cause disease. Spores that are made too large do not remain suspended in the air when released and drop to the ground and are thus never inhaled in the first place. Optimal sized spores for an anthrax biological weapon measure 1-5 micrograms in diameter.
- A person may initially have no specific respiratory or breathing symptoms but might have a low-grade fever and a nonproductive cough. An exposed person may feel chest pain early in the illness and improve temporarily before rapidly progressing to having severe breathing problems.
- Inhalational anthrax progresses rapidly with high fever, severe shortness of breath, rapid breathing, bluish color to the skin, a great deal of sweating, vomiting blood, and chest pain that may be so severe as to seem like a heart attack.
- Inhalational anthrax usually causes death when the poisonous toxins produced by the bacteria overwhelm the body systems.
- Intestinal anthrax
- Swallowing spores may cause intestinal anthrax 2-5 days later.
- People with intestinal anthrax may have nausea, vomiting (also vomit blood), tiredness, no appetite, abdominal pain, and bloody diarrhea, plus a fever.
- Intestinal anthrax is difficult to recognize. Shock and death may occur 2-5 days after it begins.
- Oropharyngeal (mouth and throat) anthrax
- Swallowing of spores may result in anthrax appearing in the mouth and throat 2-7 days after exposure.
- People with this type of anthrax may have a sore throat on one side or difficulty swallowing.
- Death may occur because the person’s throat may swell and cause difficulty breathing.
- Septicemic (bloodstream) anthrax
- Septicemic anthrax refers to an overwhelming blood infection by anthrax. This can be a complication of inhalational anthrax.
- Internal organs may become darkly colored with widespread bleeding. The bacteria multiply in the blood and overwhelm the red blood cells. The term anthrax is derived from the Greek word for coal and was descriptive in that the lesions produced turned black.
- Most cases of septicemic anthrax occur following inhalational anthrax. The number of organisms released from the liver or spleen into the bloodstream overwhelm the body’s defenses and produce massive amounts of lethal toxin that result in shock and death.
- Anthrax meningitis
- This type of anthrax may complicate any form of anthrax and spread throughout the central nervous system and to the brain.
Home Care
There is no home care for anthrax before a doctor makes the diagnosis.
When to Seek Medical Care
Anthrax develops rapidly, so immediate medical attention is required. Go to a hospital’s emergency department if you have been or think you have been exposed to spores.
Physician Diagnosis
- The skin lesions will eventually turn black. If you have a painless ulcer (sore) that is suspected to be cutaneous anthrax, the doctor will take a small sample of the fluid and see if it grows under special conditions in the laboratory. Samples will be viewed under a microscope. The anthrax bacteria will look different than other, similar organisms. If anthrax is suspected, laboratory personnel will take special care with the sample because it is considered a biohazard. Anthrax is not contagious from person to person, however, and standard hospital practices of hygiene, known as universal precautions, will prevent spread from one person to another.
- If you have cutaneous anthrax and have developed a fever and other symptoms throughout your body, the doctor may test your blood for the bacteria.
- If the doctor thinks you may have inhalational anthrax, you will have a chest x-ray or a CT scan. Other tests may be performed, including a lumbar puncture (spinal tap). You will also be admitted to the hospital.
- An infectious disease specialist may be among the doctors called in.
Anthrax Treatment
The preferred way to treat anthrax is with antibiotics. The goal of antibiotics is to destroy the infection and prevent complications and death.
- Many antibiotics are effective against B anthracis and include the following:
- Doxycycline (Vibramycin)
- Penicillin
- Amoxicillin (Trimox, Amoxil, Biomox)
- Ampicillin (Marcillin, Omnipen, Polycillin, Principen, Totacillin)
- Ciprofloxacin (Cipro)
- Levofloxacin (Levaquin)
- Gatifloxacin (Tequin)
- Chloramphenicol (Chloromycetin)
- Severely ill people may be given medications through an IV. Treatment may continue for several weeks.
- People exposed to anthrax may be given preventive antibiotics usually to be taken for 60 days.
Prognosis and Follow-up
- Prognosis: If treated early, people with cutaneous anthrax recover. Those with oropharyngeal or intestinal anthrax have a less favorable outcome, and people with inhalational anthrax have the worst outcomes. About one-half of the victims of the fall 2001 anthrax attacks died.
- Follow-up: With cutaneous anthrax, 80% of people who are not treated will recover. If treated, they may be given medication and sent home. A permanent circular scar may remain at the site of the original lesion. For others, with inhalational, meningeal, or septicemic anthrax, hospitalization is required.
Prevention
An anthrax vaccine exists but is not readily available. It consists of a series of 6 immunizations given over 18 months. A booster is then available to be given annually, especially to those who have exposure to anthrax-containing animals or animal products. A skin test can determine if the vaccine is active.
To prevent infection from spores of B anthracis released in the air after a suspected bioterrorist attack, your doctor may prescribe ciprofloxacin or doxycycline for 60 days. Other antibiotics may be used once lab tests return showing which ones are effective.
Multimedia
Media file 1: Microscopic picture of anthrax. Image courtesy of AVIP agency, Office of the Army Surgeon General, US.
Media type: Photo
Media file 2: Cutaneous (skin) anthrax. Picture courtesy of AVIP agency, Office of the Army Surgeon General, US.
Media type: Photo
Media file 3: Skin lesion of anthrax on face. Picture courtesy of the Public Health Image Library, CDC, Atlanta, Georgia.
Media type: Photo
Media file 4: Skin lesions of anthrax on neck. Picture courtesy of the Public Health Image Library, CDC, Atlanta, Georgia.
Media type: Photo
Media file 5: Chest x-ray showing widened chest cavity resulting from inhalation anthrax. Image courtesy of Dr. P.S. Brachman, Public Health Image Library, CDC, Atlanta, Georgia.
Media type: X-RAY
Media file 6: Bioterrorist Agents. Signs and symptoms to watch for. Chart courtesy of North Carolina Statewide Program for Infection Control and Epidemiology (SPICE), copyright University of North Carolina at Chapel Hill.
Media type: Acrobat PDF
Synonyms and Keywords
anthrax, bioterrorism, terrorism, spore, Bacillus anthracis, cutaneous anthrax, skin anthrax, inhalation anthrax, gastrointestinal anthrax, pulmonary anthrax, intestinal anthrax, septicemic anthrax, oropharyngeal anthrax, anthrax meningitis, woolsorter's disease
References
1. Brachman P, Friedlander AM. Vaccines. In: Plotkin SA, Orenstein WA. Anthrax. Philadelphia: WB Saunders; 1999:629-37.
2. CDC. Bioterrorism alleging use of anthrax and interim guidelines for management--United States, 1998. MMWR Morb Mortal Wkly Rep. Feb 5 1999;48(4):69-74. [Medline].
3. Christopher GW, Cieslak TJ, Pavlin JA, Eitzen EM. Biological warfare. A historical perspective. JAMA. Aug 6 1997;278(5):412-7. [Medline].
4. Cieslak TJ, Eitzen EM. Clinical and epidemiologic principles of anthrax. Emerg Infect Dis. Jul-Aug 1999;5(4):552-5. [Medline].
5. Cunha BA. Doxycycline re-revisited. Arch Intern Med. May 10 1999;159(9):1006-7. [Medline].
6. Cunha BA. Doxycycline. Antibiotics for Clinicians. Vol 3. 1999:21-33.
7. Cunha BA, Domenico P, Cunha CB. Pharmacodynamics of doxycycline. Clin Microbiol Infect. May 2000;6(5):270-3. [Medline].
8. Cunha CB. Anthrax: Ancient Plague, Persistent Problem. Infect Dis Pract. 1999;23(4).
9. Dixon TC, Meselson M, Guillemin J, Hanna PC. Anthrax. N Engl J Med. Sep 9 1999;341(11):815-26. [Medline].
10. Dragon DC, Rennie RP. The ecology of anthrax spores: tough but not invincible. Can Vet J. May 1995;36(5):295-301. [Medline].
11. Friedlander AM. Anthrax: clinical features, pathogenesis, and potential biological warfare threat. Curr Clin Top Infect Dis. 2000;20:335-49. [Medline].
12. Inglesby TV, Henderson DA, Bartlett JG, Ascher MS, Eitzen E, Friedlander AM. Anthrax as a biological weapon: medical and public health management. Working Group on Civilian Biodefense. JAMA. May 12 1999;281(18):1735-45. [Medline].
13. Kadlec RP, Zelicoff AP, Vrtis AM. Biological weapons control. Prospects and implications for the future. JAMA. Aug 6 1997;278(5):351-6. [Medline].
14. Lalitha MK, Mathai D, Thomas K. Anthrax: a continuing problem in southern India. Salisbury Med Bull Suppl. 1996;87:14-15.
15. Meselson M, Guillemin J, Hugh-Jones M, Langmuir A, Popova I, Shelokov A. The Sverdlovsk anthrax outbreak of 1979. Science. Nov 18 1994;266(5188):1202-8. [Medline].
16. Office of the Surgeon General. Medical aspects of chemical and biological warfare. Washington, DC: US Dept of the Army; 1997:467.
17. Pile JC, Malone JD, Eitzen EM, Friedlander AM. Anthrax as a potential biological warfare agent. Arch Intern Med. Mar 9 1998;158(5):429-34. [Medline].
18. Plotkin SA, Brachman PS, Utell M. An epidemic of inhalation anthrax, the first in the twentieth century. Am J Med. 1960;29.
19. Shlyakhov E, Rubinstein E. Evaluation of the anthraxin skin test for diagnosis of acute and past human anthrax. Eur J Clin Microbiol Infect Dis. Mar 1996;15(3):242-5. [Medline].
20. Shlyakhov EN, Rubinstein E. Human live anthrax vaccine in the former USSR. Vaccine. Jun 1994;12(8):727-30. [Medline].
21. Stepanov AV, Marinin LI, Pomerantsev AP, Staritsin NA. Development of novel vaccines against anthrax in man. J Biotechnol. Jan 26 1996;44(1-3):155-60. [Medline].
Authors and Editors
Author: Burke A Cunha, MD, Professor of Medicine, State University of New York at Stony Brook School of Medicine; Chief, Infectious Disease Division, Winthrop-University Hospital.
Editors: Jerry L Mothershead, MD, Special Advisor to the Navy Surgeon General for Prehospital Care, Senior Medical Consultant, Navy Medicine Office of Homeland Security, Department of Emergency Medicine, Portsmouth Naval Medical Center; Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, ; Raymond J Roberge, MD, MPH, FAAEM, FACMT, Clinical Associate Professor of Emergency Medicine, University of Pittsburgh School of Medicine; Consulting Staff, Department of Emergency Medicine, Magee-Women's Hospital of the University of Pittsburgh Medical Center.