Professor of Biology and Chemistry
University of Cincinnati Clermont College,
Batavia OH 45103
from a prepared slide
Prepared for the web 16 October 2001
This page has been accessed times since 16 October 2001.
from a prepared slide
|Bacterial Traits||Geographical Distribution||Epidemiology||Pathology||Infection||Signs and Symptoms||Treatment & Control|
ANTHRAX OBSESSION is sweeping the nation these days, and we see irrational
responses with increasing frequency. I would urge that we base our actions
less on terror and hysteria and more on what science knows about the
disease: how it is spread, how to prevent contracting it, and how to treat
patients who have contracted it. I would make several points:
1) Wash your hands. Anthrax is primarily a disease of the skin. Soap and water will remove the vast majority of spores, should you become contaminated with them. Keep your fingers out of your nose. Thorough cleansing is a key to avoiding problems in the first place.
2) Cutaneous infections are most likely when spores contaminate a wound or are scratched into the skin. These infections produce sores which are easy to recognize, and easy to treat.
3) Pulmonary infections are much more difficult to contract than cutaneous. They are more likely in persons with acute respiratory infections or otherwise debilitated. Once contracted, early diagnosis is important but difficult because the symptoms are "flu-like." A combination of chest pain, dry cough, profuse sweating and deep feeling of "not being oneself" should raise concern.
4) Treatment (in the extreme unlikelyhood that you contract anthrax) is most straight forward with simple penicillin G. Erythromycin, tetracycline and a variety of other antibiotics are also highly effective. Broad spectrum antibiotics such as Cipro (with all their deleterious side effects) are not appropriate without clear evidence that the bacteria are resistant to most antibiotics. Anthrax has little or no history of antibiotic resistance.
NOTE: I have compiled the following information on anthrax from a variety of texts and my lecture notes. It is still a "work in progress," with a few rough spots yet to be polished up. However, I believe that the facts they contain should be helpful in current discussion about the perceived threat from anthrax.INTRODUCTION
Roots of Anthrax in Germ Warfare
The British in 1941 tested an aerial anthrax bomb on tiny Gruinard Island off the coast of Scotland. The 60 sheep placed there as 'guinea pigs" were all killed by the germ warfare bonb. Unfortunately, the island remained contaminated with viable anthrax spores for more than 40 years, making it uninhabitable until protests in the 1980s led the British government to sterilize the entire island with burning followed by treatment with formaldehyde.(!) The United States actively pursued the development of anthrax as a biological weapon. It seems be significant that the strain which was used in the US attacks during the Fall of 2001 appear to be identical to one developed by the US Army for germ warfare.
TRAITS OF THE ANTHRAX BACTERIUM:
Bacillus anthracis, the causative agent of anthrax, is a large Gram positive rod, forming serpentine chains (streptobacilli) with ends squared off at regular intervals. They are facultative anaerobic bacilli. They are easy to culture, forming sticky colonies, with tiny "medusa heads" extending out. It liquefies gelatin, stabs producing "inverted fir tree" in the gelatin. It is distinguished from other Bacilli by its non-motility and presence of a capsule.
spores (central spores no wider than bacterium) are seen in 2-3
day old cultures, but not in clinical specimens. They resist heat and
certain antiseptics for moderate periods of time.
capsule is a polypeptide of poly D-glutamic acid, and is a hapten (forms active antigen when combined with other molecules).
colonies are round, and appear like "cut glass" or "ground glass" in transmitted light. They are gray and non-hemolytic on Blood Agar.
toxin: three heat-labile components, none are active alone. The virulence factor potentiates other two factors
lethal factor PA + LF = death (found in plasma of dying animals)Virulence associated with rough colonies (?).
edema factor PA + EF = edema
virulence dependant on (single) capsule (anti phagocytic) and toxins.
Anthrax is primarily disease of herbivores, especially sheep, goats, cattle and horses. It infects man rarely. The agent is found in soil and on vegetation upon which grazing animals become infected through injured mucous membrane, when spores are found on spiny or irritating vegetation.. Spores are released in great numbers when the animal dies and decomposes, contaminating both the carcass and soil. The spores enter the soil where they are viable for decades. "Incubator areas" have alkaline or neutral calcareous soils in which the bacterium can multiply under favorable conditions. Outbreaks occur primarily in warmer seasons. Biting flies may transmit during epidemic, but are thought to be of little importance. Humans are accidentally exposed via contaminated animals or animal products, a particular hazard for veterinarians and farmers.
Products (often imported) made from infected animals have caused recent human infections in the U.S. including such diverse products as bone meal, shaving brush bristles, hair or wool in textiles (especially alpaca wool, goat's and even camel's hair), hides and leather goods, goatskin drums. Handicrafters and hobbyists working with leather, hairs and wools at risk if materials from endemic areas. Oil cake and tankage made from contaminated materials can transmit anthrax.
There is considerable variation among species in susceptibility: Guinea Pig are highly susceptible and rats resistant.
Anthrax has been endemic in southern Europe, parts of Africa, Australia, Asia and North and South America. It persists in arid deserts of Middle East, Asia, Africa, Australia and South America with the most cases reported from Iran, Turkey, Pakistan and Sudan.
It is relatively rare in the US, but last year, 500+ cases in Texas were recorded in White Tailed Deer. It has occurred in livestock in South Dakota, Nebraska, Arkansas, Mississippi, Louisiana, and California as well.
In infected tissues, bacterial capsules remain intact, and the organisms become surrounded by large amount of proteinaceous fluid due to the toxins released. There are however few leukocytes in non-immune animals. The bacteria rapidly disseminate, and lymph nodes are a common site of bacterial growth, leading to enlarged, hemorrhagic nodes. The highly fatal inhalation form of the disease is due to such infested nodes in the space between the lungs, an area called the mediastinum. This hemorrhagic mediastinitis is commonly known as "wool sorters disease." From these infected nodes, the bacilli can easily reach blood.
In resistant animals, massive accumulation of leukocytes keep infection localized.
Chains of large Gm positive rods are easily distinguished by microscopic examination of a Gram stained smear of lesion pus.
Humans are moderately resistant to the disease, with 20,000 to 100,000 cases per year worldwide. Infection acquired via one of three routes, through the skin, by inhalation, or by ingestion. Cutaneous infection constitute 95% of infections, and are acquired through minor abrasion, injured skin or at pressure point of contaminated hide against skin. Rarely, it is contracted by inhalation of spores, causing "Woolsorter's disease," (often through the processing contaminated goat hair). According the to Merck Manual, "Inhaling spores under adverse conditions (e.g.. the presence of an acute respiratory infection) may result in pulmonary anthrax which is often fatal." Infections due to ingestion are rare in humans. It is not communicable from person to person. The incubation period is generally 3-5 days. Spores germinate in tissue at site of entry, lead to gelatinous edema. The pathogens spread by the lymphatics to blood stream shortly before (and after) death. It can be spread among animals via biting flies, insects and vultures, but this mode of transmission is thought to be rare.
SIGNS AND SYMPTOMS:
(from Morello et al)
|Cutaneous: In man, a malignant pustule forms: 12-36 hours after entry via a scratch, a painless but itchy red-brown papule forms. It rapidly progresses to an oozing ulcer surrounded by vesicles containing bacteria. Finally, it turns into a necrotic black ulcer (eschar) from which infection can disseminate to septicemia. This black sore give the disease its name because it appears like coal (anthrax is Latin for coal). Disseminated anthrax can lead to massive edema. Mortality for untreated cutaneous anthrax is 5 to 20%. Microscopic examination and culture of skin lesions showing large Gram-positive bacilli (no spores) is suggestive of anthrax. Specific fluorescent antibodies confirm the diagnosis.|
|Inhalation initially mimics viral respiratory illness with fatigue, fever and headache. ("flu-like symptoms"). Key differentiating signs and symptoms distinguishing inhalation anthrax include: chest pain, dry cough, profuse sweating, and a deep sense of "not being oneself." Note that it does NOT include stuffy or runny nose or sore throat characteristic of upper respiratory infections. It rapidly progresses to diffuse pulmonary involvement, to respiratory failure. The mortality rate is high even when treated due to tardy diagnosis, ~95%.|
|Ingestion very rare in humans, but also with high mortality. Nausea, vomiting anorexia, fever are characteristic, often with bloody stool.|
Penicillin is the antibiotic of choice. For patients who are allergic to penicillin, many other antibiotics are effective, including erythromycin, tetracycline and chloramphenicol. The typical treatment for cutaneous anthrax is a 7 day course of Penicillin G, 600,000 U IM. Ciprofloxacin (Cipro) is being widely touted and there has been a stampede to buy it up by the frightened public. This broad-spectrum antibiotic is very expensive and has serious possible side effects. It is an illogical choice to treat anthrax, especially when simple penicillin G is effective and readily available. Furthermore, doctors should not be prescribing antibiotics for patients in the absence of indications. It only contributes to the appearance of antibiotic resistant bacteria.
Because the anthrax bacterium has had little exposure to penicillin it is likely to be sensitive to it (as opposed to many other common bacterial infections). Indeed, widespread use of Cipro against this anthrax is unwise because it will favor development of resistance in common pathogens. As always, no antibiotics should be taken without clear indication of bacteria infection.
Basic polypeptides kill anthrax, including polylysine.
Herds at risk should be vaccinated, and animals infected should be culled immediately, and all anthrax-infected carcasses should be burned or buried in deep lime pits. It is difficult to eradicate due to long-lived spores in soil, with no easy method of disinfecting soil.
Vaccination with live attenuated bacilli was suggested by Pasteur, who, in 1881, grew the bacteria at 42-43 C for several months. This is near the limit of temperature requirement for the bacillus. After repeated culture at this elevated temperature, he found that it had lost much of its virulence, and when injected into cattle and sheep, protected them from infection. However, this protection may not be of long duration. Humans who are at particular risk can be vaccinated as well (veterinarians, animal handlers, persons working with animal carcasses or products, etc).
Animal products which can carry spores can be autoclaved to destroy
the spores: hides, bristles, hair.
All work with Bacillus anthracis should be carried out in biological safety cabinet. Protective clothing and gloves worn gloves should be used when handling infected animals.
The following texts have been used to prepare these notes:
Alcamo, Fundamentals of Microbiology, 5th Ed., (1996).
Beers & Berkow, Editors, Merck Manual 15th Ed, (1999). p 1157
Birge, Edward, Modern Microbiology Principles and Applications, (1992). p373.
Budavari, Ed, Merck Index, 11th Ed, (1989)
Jawetz et al. Review of Medical Microbiology, 9th, (1970).
Morello et al, Microbiology in Patient Care, (1994) (See color plate 12c, opposite page 487 for picture.)
Murray et al, Medical Microbiology, 2nd, (1994)
Totora, Funke and Case, Microbiology, An Introduction, 7th Ed., (2001). p. 631,