Borrelia burgdorferi

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A Microbial Biorealm page on the genus Borrelia burgdorferi

Classification

Higher order taxa

Bacteria; Spirochaetes (Phylum); Spirochaetes (Class); Spirochaetales; Spirochaetaceae

Species

Borrelia burgdorferi

NCBI: Taxonomy

Description and significance

Borrelia burgdorferi bacterium, CDC

Borrelia burgdorferi is a Gram-negative spirochete bacteria that is well known as the causative agent of Lyme disease. In 1982, a few years after Lyme disease was first diagnosed, it was determined that B. burgdorferi was being transmitted to humans by ticks. Since then, it's genome has been fully sequenced and researchers have been able to study the interesting mechanism of host and vector transmission that the bacteria has adopted. However, the exact mechanisms for its pathology are still trying to be understood. B. burgdorferi is currently being used to answer interesting questions surrounding vector transmission, host adaptation and plasmid maintenance (Rosa). According to the Center for Disease Control, Lyme disease caused by B. burgdorferi has become the most common vector-borne bacterial disease in the world. B. burgdorferi's unique structure and adaptations allow it to be an effective invasive pathogen and an important organism to research.

Genome structure

B. burgdorferi has a very unique genome. It consists of one large linear chromosome that is 910,725 base pairs long. This chromosome contains approximately 853 genes coding for basic functions such as DNA replication, transcription, translation as well as transport and metabolic systems. However, in addition to this chromosome, the bacterium also contains 21 other linear and circular plasmids that add an additional 533,000 base pairs of DNA. The genomic organization of B. burgdorferi is unique due to the high number of plasmids. Research has shown that some bacteria lacking a complete set of plasmids are unable to successfully infect their host, leading researchers to believe that the plasmids may encode virulent DNA (Fraser). One plasmid named lp25 has been found to be necessary for Borrelia infection. An lp25 gene named BBE22 has been discovered to encode for a nicotinamidase which by itself can maintain the ability for the bacteria to infect the host even when the plasmid is removed (Purser). However, in general, the sequenced genome does not contain any obvious genes coding for pathogenesis, and therefore, the mechanisms of B. burgdorferi infections are still a hot topic of research.

Cell structure and metabolism

B. burgdorferi is a helical shaped spirochete bacterium. It has an inner and outer membrane as well as a flexible cell wall. Inside the bacteria's cell membranes is the protoplasm, which, due to the spiral shape of the bacteria, is long and cylindrical. The cell is normally only 1 μm wide but can be 10-25 μm long. Spirochete bacteria such as B. burgdorferi have a unique structural characteristic. The cell's flagella are located inside the periplasm between the inner and outer cell membranes. The interactions between the flagella and cell cylinder allows the cell to travel through highly viscous fluids and materials (Charon). This adaptation is especially critical for the ability of B. burgdorferi to travel through the tissue of its infected host or vector, causing it to be highly invasive.

Structure of Borrelia burgdorferi, Reprinted by permission from Nature Publishing Group: Nature Reviews Microbiology, copyright 2005

Another important cellular component of B. burgdorferi is its outer surface proteins. Researchers have investigated a variety of outer membrane surface proteins (Osp) and have found them to play important roles in transmission of the bacteria. The cell expresses different surface proteins, most notably OspA and OspC. However, they are not seen on all cells. When the bacteria is inside of an unfed tick, it produces mostly OspA. However, the bacteria that are inside of infected mammals express mostly OspC (Schwan). This has caused speculation that the bacteria produces specific outer surface proteins in order to successfully invade and inhabit certain organisms. For example, OspA may function to retain the bacteria in the tick stomach, while the presence of OspC may encourage the bacteria to enter the salivary glands and enter the host (Ohnishi). OspA, OspC, and other outer surface proteins may play important roles in the ability of the bacteria to infect and survive inside their hosts.

The genome sequencing of B. burgdorferi showed that it has genes for metabolism similar to other parasites. These bacteria have limited metabolic capabilities and rely on their host for energy precursors. The genome of B. burgdorferi encodes many transport proteins such as ABC transporters and enzymes and proteins used in the phosphotransferase system. These transport systems are likely used to obtain compounds from the host serum or environment. B. burgdorferi uses glucose and other similar carbohydrates as its main energy source in mammals. In ticks, it is believed that N-acetylglucosamine (NAG) is a major energy source as it is a main component of tick cuticle and is essential for in vitro growth of the bacteria. B. burgdorferi does not contain genes or enzymes for the TCA cycle, oxidative phosphorylation or an electron transport chain. Instead, it produces ATP solely by using substrate-level phosphorylation and achieves reducing power using the pentose phosphate pathway (Fraser).

Ecology

Borrelia burgdorferi is maintained in a natural cycle of infection by ticks. The ticks acquire and transmit the bacteria by feeding on a variety of small mammals and birds that act as a reservoir host for the Borrelia. B. burgdorferi is transmitted specifically by ticks of the genus Ixodes, which include a variety of different species found in different geographical locations. Ixodes scapularis is the most common vector and is found in the Northeastern US. Ixodes pacificus is found on the west coast, while species Ixodes ricinus and persulcatus are found in Europe and Asia. These ticks acquire and transmit the bacteria to different hosts during three distinct feeding phases of their life cycle; larval, nymphal and adult stages.

B. burgdorferi is transmitted to different mammalian hosts through ticks. Reprinted by permission from Nature Publishing Group: Nature Reviews Microbiology, copyright 2005

Pathology

Lyme disease was first identified due to an outbreak of juvenile rheumatoid arthritis. This is one of the later stage symptoms of the B. burgdorferi infection. Ticks use many small mammals to harbor the bacteria, and humans only become inadvertently infected when bitten. It is believed that the bacteria use a variety of mechanisms to evade the host immune response. This includes upregulating certain outer surface proteins, or attaching themselves to immunosuppressive tick salivary proteins. Once the Borrelia has entered the host, it becomes very invasive and can spread quickly throughout the entire system. The first sign of infection is the erythema migrans, a circular rash at the site of the tick bite that appears after a few days delay. From there, infected humans may develop similar rashes on other sites of the body as well as symptoms such as fatigue, fever, headache, and muscle and joint aches. If the infection spreads throughout the body it has reached Stage II of the infection, which is marked by symptoms such as facial palsy, meningitis, extreme joint pain and heart palpitations. If it is left untreated for a few months the infection will reach Stage III and patients may develop arthritis as well as severe joint pain and swelling ("Lyme Disease," Wormser). For more on diagnosis and treatment of Lyme disease, refer to the CDC website on Lyme disease.

Erythema migrans, Ross Ritter, P.A.

Application to Biotechnology

Borrelia burgdorferi is well studied pathogen that causes Lyme disease. Most of the research on this bacteria is focused on understanding the vector and host transmission as well as its pathogenic activity in order to develop better methods to prevent infection. It does not have a current, widespread use in biotechnology.

Current Research

Much of the current research surrounding B. burgdorferi concentrates on discovering the mechanisms through which the bacteria invades the human body in order to produce more effective treatments against it. As a member of the Spirocheate phylum, B. burgdorferi is quite distinct from many other bacterial groups and therefore many of the common genetic tools do not work on the bacteria. It is also very difficult to transform in the laboratory.

The most current research of B. burgdorferi surrounds the discovery of the immunosuppressive tick salivary protein, Salp15. This protein is believed to be involved in the transmission of the bacteria from the vector to the host. It is believed that the tick produces Salp15, which binds to B. burgdorferi and protects it from the host antibody response (thus earning its immunosuppressive title). This makes Salp15 an attractive target for research and possible use in vaccines ("Transmission").

In April 2007, Juncadella and colleagues determined that Salp15 inhibited T-cell activation by interfering with the binding of CD4 receptors o nT-cells and disrupting their signalling cascade. The researchers were able to identify the C-terminal peptide of Salp15 as responsible for its immunosuppressive properties. They confirmed that the Salp15-CD4 interactions caused premature activation and a defective immune response. These results can help future researchers uncover methods to block the activity of Salp15 and possibly develop an effective vaccine.

Current research is also investigating other mechanisms in which Borrelia burgdorferi is able to evade the host organisms immune response. One theory is that the bacterial outer surface proteins are able to bind to host factor H, a regulator in the complement activation pathway. By binding to this regulator, the bacteria may be able to protect themselves from complement killing. Researchers tested this theory by developing strains of mice that were deficient in host factor H in order to see whether B. burgdorferi binding was necessary for infection. Their results showed that the deficient mice were infected at similar levels to wild-type mice. In addition, control experiments showed that many of the bacteria did not bind to host factor H even when they had outer surface proteins present capable of doing so. They also showed that some mice deficient in complement activating pathways were able to contain the Borrelia infection. These results indicate that B. burgdorferi must have other mechanisms to prevent complement activation in the host, and that complement mediated killing may not be the only way for the host to combat the bacteria. The results of these experiments help us better understand the mechanisms involved in B. burgdorferi infections (Woodman).

Interesting research was also performed concerning the sensitivity of certain individuals to tick bites and whether this sensitivity could limit the ability of B. burgdorferi to infect that person. The researchers sampled a population in Rhode Island and determined that people who had more exposure to tick bites had stronger and faster reactions to the bites and also had less risk of developing Lyme disease. Their results showed that people who were frequently bitten by ticks developed an immunity against them, possibly against tick salivary antigens. Therefore, the new hypersensitivity may be able to protect this individuals from Borrelia infection and help them recognize tick bites and remove them before the bacteria can be transmitted. These results lend support to the idea that immunity against tick salivary proteins may help prevent infection by B. burgdorferi and therefore the symptoms of Lyme disease (Burke).

References

Burke G, Wikel SK, Spielman A, Telford SR, McKay K, Krause PJ, et al. "Hypersensitivity to Ticks and Lyme Disease Risk." Emerging Infectious Disease. 2005 Jan. Volume 11(1), p. 36-41.

Charon, NW., Greenberg, EP., Koopman, MBH., and Limberger RJ. "Spirochete chemotaxis, motility, and the structure of the spirochetal periplasmic flagella." Research in Microbiology. 1992. 143(6). p. 97-603.

Fraser, CM., Casjens, S., Huang, WM., Sutton, GG., Clayton, R. et al. "Genomic sequence of a Lyme disease spirochaete, Borrelia burgdorferi." Nature. 1997 Dec 11;390(6660):580-6.

Juncadella IJ, Garg R, et al. "T-cell signaling pathways inhibited by the tick saliva immunosuppressor, Salp15." FEMS Immunology & Medical Microbiology. 2007 April. 49(3). p. 433-438.

"Lyme Disease." Center For Disease Control: Division of Vector-Borne Infectious Diseases.

Motaleb, MA. et al. "Borrelia burgdorferi periplasmic flagella have both skeletal and motility functions." Proceedings of the National Academy of Sciences of the USA. 2000 Sept 26. Volume 97(20). p. 10899−904.

Ohnishi J, Piesman J, De Silva AM. "Antigenic and genetic heterogeneity of Borrelia burgdorferi populations transmitted by ticks." Proceedings of the National Academy of Sciences of the USA. 2001 Jan 16. Volume 98(2). p. 670-675.

Purser JE, Lawrenz MB, Caimano MJ, Howell JK, Radolf JD, Norris SJ. "A plasmid-encoded nicotinamidase (PncA) is essential for infectivity of Borrelia burgdorferi in a mammalian host." Molecular Microbiology. 2003 May. Volume 48(3), p. 753–764.

Rosa, PA., Tilly, K., and Stewart, PE. "The Burgeoning Molecular Genetics of the Lyme Disease Spirochaete." Nature Reviews Microbiology. 2005. Volume 3(2), p. 129-143.\

Schwan TG, Piesman J, Golde WT, Dolan MC, Rosa PA. "Induction of an outer surface protein on Borrelia burgdorferi during tick feeding." Proceedings of the National Academy of Sciences of the USA. 1995 Mar 28. Volume 92(7). p. 2909-13.

"Transmission of Lyme Disease." National Institute of Allergy and Infectious Disease: National Institute of Health.

Woodman ME., Cooley AE., et al. "Borrelia burgdorferi Binding of Host Complement Regulator Factor H Is Not Required for Efficient Mammalian Infection." Infection and Immunity. 2007 June. Volume 75(6), p 3131-9.

Wormser GP., et al. "The clinical assessment, treatment, and prevention of lyme disease, human granulocytic anaplasmosis, and babesiosis: clinical practice guidelines by the Infectious Diseases Society of America." Clinical Infectious Diseases. 2006 Nov 1. Volume 43(9), p. 1089-1134.

Edited by Dan Holligan, student of Rachel Larsen and Kit Pogliano at UCSD.