The Role of Clostridium perfringens Toxins in Gas Gangrene

From MicrobeWiki, the student-edited microbiology resource

What is Gas Gangrene and What Causes It?


By Marysol Arce


A patient's right thigh severely affected by gas gangrene. Courtesy of Cases Journal, 2008, Vol. 1, Issue 252, published on BioMed Central (http://casesjournal.biomedcentral.com/articles/10.1186/1757-1626-1-252.

Gas gangrene is caused by a rod shaped, gram positive, spore forming bacterium called Clostridium perfringens. The bacterium lives in anaerobic environments like the soil and inside the gut of humans and animals (Williamson and Titball 1993). Clostridium perfringens is currently known to have five different strains, marked as: A, B, C, D, and E (Sakurai et al. 2004). The different strains are classified based on which toxins they produce: alpha toxin, beta toxin, epsilon toxin, and/or iota toxins (Shimizu et al. 2001). The Clostridium perfringens A strain is of the most importance because it causes gas gangrene, or myonecrosis, in humans. Gangrene is the death of body tissue and usually seen in elderly people or diabetic people. Open wounds or trauma into deep tissue that become infected by bacteria also become gangrenous. Gas gangrene is an especially dangerous form because it spreads quickly throughout the body if left untreated, and can be fatal. C. perfringens produces toxins that kills cells and releases gas, leaving parts of the body black, purple, and covered with blisters. The A strain of the C. perfringens bacterium produces two important toxins that enable the spread of the bacterium and tissue death: the alpha toxin and perfringolysin O (O’Brien and Melville 2004). The alpha toxin, also known as CPA or PLC, is a crucial virulence factor for this bacterium because gas gangrene cannot occur without it. However, the alpha toxin and perfringolysin O (PFO) work synergistically to accomplish the spread of infection (Awad et al. 2001). The toxins can cause septic shock (when infection leads to very low blood pressure) and hypoxia (reduced amounts of oxygen to body tissues). It even causes organ failure and muscle degeneration due to the lack of oxygen and reduced blood flow. The degeneration of the muscle and tissue releases gas that builds up under the skin and makes the area blister and bubble. The appearance of these blisters in various parts of the body usually indicates that the infection has progressed very far and that the tissue is decomposing. The body’s immune system is also rendered helpless because the toxins make the leukocytes clump together and clog in the blood vessels (leukostasis), unabling them to get to the site of infection (Stevens and Bryant 2002). The toxins also cause further blood vessel dysfunction, like vascular leakage which is what makes swelling a big characteristic of this disease.

Clostridium perfringens genome

The bacterium Clostridium perfringens’ genome is a lone circular chromosome with additional plasmids that are extra-chromosomal, meaning that there is other DNA found outside of the nucleus (Verherstraeten et al. 2015). It is made up of 2,660 regions that encode proteins and 10 ribosomal RNA genes (Shimizu et al. 2002). The genome also possesses the anaerobic fermentation enzymes usually found in bacterium that allow for gas production. However, it does not have any tricarboxylic acid (TCA) cycle enzymes or for a respiration mechanism. Many saccharolytic enzymes are present but most of the enzymes needed in amino acid biosynthesis are not present in the genome. There are at least 20 genes that encode virulence factors for the bacterium and 5 hyaluronidase genes, which encode enzymes that degrade hyaluronic acid, that also add to C. perfringens virulence (Shimizu et al 2001). There are also 4 regulons that regulate the pathogenicity, the ability of the organism to cause disease, of the bacterium. Clostridium perfringens utilizes and gains many different crucial materials needed to perform their function from the host cells by producing many degradative toxins and enzymes. To obtain what they need, the bacterium uses these toxins and enzymes to destroy the host’s tissues and cells. The two critical toxins of C. perfringens A strain, alpha toxin and perfringolysin O, are both chromosomally encoded (Li et al. 2013).




Other examples:
Bold
Italic
Subscript: H2O
Superscript: Fe3+


Introduce the topic of your paper. What is your research question? What experiments have addressed your question? Applications for medicine and/or environment?


A citation code consists of a hyperlinked reference within "ref" begin and end codes. [1]

Alpha Toxin (PLC)

Include some current research, with at least one figure showing data.

Every point of information REQUIRES CITATION using the citation tool shown above.

All strains of C. perfringens produce the alpha toxin, also called CPA or PLC. The alpha toxin cleaves molecules from the surface the host cell's’ phospholipid bilayers and disrupts the membrane’s functions, which then promotes cell lysis and death.

Alpha toxin attachment and insertion into host cell membrane. Courtesy of The Jounal of Biochemistry, 2004, Vol. 136, Issue 5, 569-574, published on Oxford Journals (http://jb.oxfordjournals.org/content/136/5/569.long.

Perfringolysin O (PFO)

Include some current research, with at least one figure showing data.


Perfringolysin O binding with the phospholipid bilayer. Courtesy of Toxins Journal, 2015, Vol. 7, Issue 5, 1702-1721, published on MDPI: Open Access (http://www.mdpi.com/2072-6651/7/5/1702/htm.

How Do These Toxins Help C. perfringens Persist and Spread in the Body?

Include some current research, with at least one figure showing data.

Conclusion

References

Schröpfer, Engelbert, Stephan Rauthe, and Thomas Meyer. "Diagnosis and Misdiagnosis of Necrotizing Soft Tissue Infections: Three Case Reports." Cases Journal 1.252 (2008): n. pag. BioMed Central. Web. 21 Apr. 2016.

Awad, Milena M., Darren M. Ellemor, Richard L. Boyd, John J. Emmins, and Julian I. Rood. "Synergistic Effects of Alpha-Toxin and Perfringolysin O in Clostridium Perfringens-Mediated Gas Gangrene." Infection and Immunity 69.12 (2001): 7904-910. American Society for Microbiology. Web. 18 Apr. 2016.