The pathogenesis of Bacillus anthracis
By [Tony Amolo]
Anthrax is an infectious disease caused by the bacteria Bacillus anthracis. Bacillus anthracis is a microorganism from the family Bacillaceae (Figure 1). Unlike other bacillus microorganisms which are harmless saprophytes, Bacillus anthracis is an obligate bacillus pathogen that infects many vertebrates. Based on its physical characteristics, Bacillus anthracis can be categorized with other microorganisms such as Bacillus cereus, Bacillus thuringiensis and Bacillus mycoides. This categorization exists because it is difficult to characterize these organisms based on their 16s rRNA sequences (10). Organisms from the bacillus genus are mostly extremophiles. They have the ability to grow in severe conditions which other microorganisms cannot withstand (4).
Anthrax is as old as man, it was given its name by a Greek physician named Hippocrates because of the black sore it causes on the skin of human and animals(1). It generally affects warm blooded animals including humans. Aloys Pollender, a German physician who was acknowledged for identifying the disease described Bacillus anthracis as “chyllus corpuscles” after analyzing the abdomen of infected cows that had died of anthrax (2). Anthrax was broadly studied in the 1870s by Robert Koch and Louis Pasteur. Koch applied the suspended drop culture method to understand the life cycle of the bacteria and found that the spores formed could survive for long period in harsh environment (3).Koch’s studies on Bacillus anthracis helped him come up with the germ theory of disease.
Cell Structure and Metabolism
Bacillus anthracis is a gram positive, endospore forming bacteria (Figure 2). It is capsulated, immobile and rod shaped. Bacillus anthracis has the ability to make ATP in the presence or absence of oxygen and cannot be seen unless with a microscope. It is 5-6 micrometer long, 1-1.5micrometer wide and looks like bamboo canes in tissue (13). Despite its small size, the diverse abilities of many species of its genus allows them to survive in different environments (4). They have the ability to form chains, colonies and biofilms.
Habitat and Ecology
Bacillus anthracis is a soil borne bacteria. It lives best in black steppe soils with lots of calcium and at pH levels between (7-9). Endemic anthrax areas have been associated with warmer temperatures, higher soil moisture content and topography (15).
Spore Formation, Anatomy and Germination
Bacillus anthracis forms one endospore per cell. Its spores form when its non reproductive cells are deficient of certain nutrients . The spores are oval in shape and sporulation occurs within 48 hours. Bacillus anthracis requires oxygen to sporulate. Spores can tolerate heat, cold, dehydration, radiation and even antibacterials (8). The formation of spore commences when cells septate asymmetrically to create a forespore and a mother cell. After septation, the mother cell swallows the forespore and covers it with different layers. The spore is made up of several layers. These layers are the coat, the exosporium and the cortex (Figure 3). The innermost layer is the core. It contains proteins which holds the chromosome. Half of the spore is composed of the spore coat. The flexibility of the spore coat enables the spore to hold the core especially during germination. It protects the spore from harmful chemicals and aids germination. The cortex containing peptidoglycan protects the spore from radiation, heat and makes the core dry. The exosporium is the outermost layer of the spore. It is a protein rich, balloon-like, loose fitting structure covering a spore(8). The exosporium has been studied to understand the use of anthrax as a weapon because of its quality and unique structure. The disintegration of the mother cell to produce the spore indicates the completion of spore formation. The mature spores have a structured arrangement that enables them withstand and endure physical damage and severe environmental conditions. Outside a host, the mature spores of Bacillus anthracis are inactive. Upon entry into a host, they have the ability to germinate and become non reproductive cells that can easily replicate all around the host's internal organs and cause damage.The availability of host’s environment with sufficient nutrients causes germination to occur (17). Non reproductive cells transform back to spores whenever the host dies. Germination and growth of spores in the host cells are essential for the release of its virulence factors.
Pathogenesis and Virulence factors
Bacillus anthracis contains two toxic plasmids: the pX01, which produces the edema factor, the protective antigen and the lethal factor, and the pX02, which encodes the production of the capsule. Bacillus anthracis carries out its pathogenic process by using its capsule and producing toxics consisting of three proteins(EF, LF and PA). (13) The combination of lethal toxin, which constitutes the protective antigen and the lethal factor and edema toxin which constitutes the protective antigen and the edema factor can induce severe cases of the disease(7). Out the three factors, the protective antigen plays a crucial role in the toxic action of Bacillus anthracis (Figure 4). Protective antigen is important in anthrax poisoning because it allows the connection and entry of the lethal factor and Edema factor into the cytosol. It also helps bind the cell receptor, the lethal factor and the edema factor to the host cell. Protective antigen is a primary antigen that exists in anthrax vaccines(11). The edema factor is a cyclase that causes an imbalance of water homeostasis. The edema toxin may increase host susceptibility to infection by disrupting the cytokine response of monocytes and by suppressing neutrophil functions (11). The lethal factor is a metalloprotease that cleaves major pathways to surface receptors for the transcription of certain genes within the nucleus(12) while the capsule enhances the virulence by inhibiting the phagocytosis of Bacillus anthracis.
Transmission and Pathology
The common ways of transmission of the anthrax disease are through wounds, the pharynx, gastrointestinal tract, the digestive system after ingesting spore contaminated food or water, skin lesions or abrasions caused by biting flies and the breathing in of air containing anthrax spores. After transmission through one of these route, the spores travel to the lymph nodes where they begin to multiply rapidly and the produce spores which germinate to produce the virulence factors (13).
Vaccines and Treatment
Anthrax was the first bacterial disease for which effective preventive treatment (prophylaxis) was developed(11). Prophylaxis played a major role in controlling anthrax in animals and protection to individuals from infection. Several vaccines has been produced for the anthrax disease. Louis Pasteur is known as the first microbiologist to produce the first anthrax vaccine in 1881 (2). The vaccines were made of spores from weakened genetic variant of Bacillus anthracis. Vaccines produced to combat the disease include non-living vaccines, In vitro protective antigen, Boor and Tresselt vaccine, production in non-proteinaceous media, UK vaccine, American vaccines(Aerobic antigen and Anaerobic antigen) and Russian antigen (6). Special therapy can also be provided to treat anthrax if it is applied immediately to the infected animal or human. Aside from vaccines, antitoxin and antibiotics have been used to treat the disease. Penicillin, ciprofloxacin and doxycycline have been used to treat the susceptible genetic variants of anthrax.(14) Different methods have been adopted to create an enhanced vaccine for humans. The objective is to develop a vaccine that is non reactogenic and involves little administration to perform efficiently (11). However, the difficult aspect of checking the potency of anthrax vaccine is making an assessment in humans. Tests using this pathogenic bacteria is not safe for humans and animals and requires special precautions.
Application to Bioterrorism
Out of many pathogenic bacteria, Bacillus anthracis is one that can be used for bioterrorism. Of its three types(cutaneous, inhalation and gastrointestinal), inhalation anthrax has been related to bioterrorism because of its mode of transmission. Bacillus anthracis makes a good model weapon for bioterrorism because it spores can be produced in the laboratory,it survives longer in the environment and can be found easily. Also, because of its small size, it can be placed in food and letters like in 2001 when powdered anthrax was mailed to the U.S postal office. Twenty-two cases of anthrax infections were confirmed. Half of these cases involved cutaneous anthrax and no death resulted. The remaining eleven were identified as inhalational anthrax and produced five deaths. Several countries like the past Soviet Union and Iraq have been known to produce Bacillus anthracis as a bioweapon (22). Aside from inflicting this pathogenic bacteria through letters, aerosol delivery can also be implemented. It entails aiding the bacteria travel a longer distance while keeping it odourless and unseen (22). A global awareness should be created to reject the development of anthrax as weapons and provide a better means to fight this deadly disease.
1] Annabel Guicharda, Victor Nizetb, c, Ethan Biera "New insights into the biological effects of anthrax toxins: linking cellular to organismal responses." 2012.
2] Joseph A Witkowski,Lawrence Charles Parish "The story of anthrax from antiquity to the present: a biological weapon of nature and humans."2002.
15] Jocelyn C. Mullins, Giuliano Garofolo, Matthew Van Ert, Antonio Fasanella, Larisa Lukhnova, Martin E. Hugh-Jones, Jason K. Blackburn. "Ecological Niche Modeling of Bacillus anthracis on Three Continents: Evidence for Genetic-Ecological Divergence?."2013.
21]  Hongbin Liu1, Nicholas H. Bergman, Brendan Thomason, Shamira Shallom, Alyson Hazen, Joseph Crossno, David A. Rasko, Jacques Ravel, Timothy D. Read, Scott N. Peterson, John Yates, and Philip C. Hanna. "Formation and Composition of the Bacillus anthracis Endospore."2003.
22] Thomas V. Inglesby, Tara O'Toole, Donald A. Henderson, John G. Bartlett, Michael S. Ascher,Edward Eitzen,MPH; Arthur M. Friedlander, Julie Gerberding, Jerome Hauer,James Hughes, Joseph McDade, Michael T. Osterholm, Gerald Parker,Trish M. Perl, Philip K. Russell,Kevin Tonat, DrPH. "Anthrax as a Biological Weapon, 2002 Updated Recommendations for Management"2002.