Wikipedia

Leptospira interrogans

This is an old revision of this page, as edited by Kitanana (talk | contribs) at 00:25, 13 October 2023. The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Leptospira interrogans is a species of obligate aerobic spirochaete bacteria shaped like a corkscrew with hooked and spiral ends.[1] L. interrogans is mainly found in warmer tropical regions. The bacteria can live for weeks to months in the ground or water.[2] Leptospira is one of the genera of the spirochaete phylum that causes severe mammalian infections.[3] This species is pathogenic to some wild and domestic animals, including pet dogs. It can also spread to humans through abrasions on the skin, where infection can cause flu-like symptoms with kidney and liver damage.[2] Human infections are commonly spread by contact with contaminated water or soil, often through the urine of both wild and domestic animals.[2] Some individuals are more susceptible to serious infection, including farmers and veterinarians who work with animals.[4]

Leptospira interrogans
Scanning electron micrograph of Leptospira interrogans.
Scientific classification Edit this classification
Domain: Bacteria
Phylum: Spirochaetota
Class: Spirochaetia
Order: Leptospirales
Family: Leptospiraceae
Genus: Leptospira
Species:
L. interrogans
Binomial name
Leptospira interrogans
(Stimson 1907) Wenyon 1926 (Approved Lists 1980)

The bacteria cause two phases of infection, the anicteric phase and the icteric phase. The anicteric phase of infection is commonly known as phase one, in which humans exhibit fever, headache, and nausea. The icteric phase, or phase two, includes more severe symptoms including hemorrhages and renal tubular failure.[5] The main ways for testing for bacteria and diagnosing infections include the microscopic agglutination test (MAT) and PCR.[6] Leptospirosis is treated in humans by the antibiotics penicillin and doxycycline.[7][8]

L. interrogans has many properties that ensure its optimal survival in specific conditions, including two periplasmic flagella for movement and mobility. These flagella enable L. interrogans to more easily access and infect both human and mammalian tissues.[9] The species uses beta oxidation of long chain fatty acids for energy, in which oxygen and peroxides are used as the main terminal electron acceptors.[10] The L. interrogans genome consists of two circular chromosomes.[11]

Biology and Biochemistry

Morphology

L. interrogans cells are gram-negative, tightly coiled, motile spirochetes, with two periplasmic flagella.[1] One flagellum is inserted at each end of the bacterium. The cells are thin, about 0.15 µm, and long, between 6-20 µm, with a corkscrew shaped body with spiral or hooked ends.[1] The hooked ends often resemble a question mark, and this is where the name ‘interrogans’ comes from.[12] The periplasmic flagella are crucial to the bacteria's ability to move and survive in specific host cells. The leptospires reveal two unique forms of movement, translational and non translational.[13]

Metabolism/Physiology

L. interrogans displays neutralophilic properties, growing in a pH range of 7.2 - 7.6, with an optimal pH of 7.4. The bacteria also display mesophilic growth properties and grow at a temperature range of 28 °C to 30 °C.[14][12] The optimal growth of the obligate aerobe L. interrogans occurs in simple media containing vitamins, salts, and specific long chain fatty acids.[13] Leptospira require ammonium salts as well as long-chain fatty acids for metabolism.[15]

The major energy and carbon source of this organism is the beta-oxidation of long chain fatty acids. Through naturally occurring phase interfaces or its growth media, L. interrogans must physically obtain the long chain fatty acids in order to further metabolize them as an energy source.[16] Unique to the metabolic characteristics of L. interrogans, long chain unsaturated fatty acids are required for the bacterium to grow, as saturated fatty acids can only be metabolized in these conditions.[16] L. interrogans contains genes that code for the use of the TCA cycle in its metabolism.[16] L. interrogans ATP production comes through oxidative phosphorylation.[16] Oxygen serves as the terminal electron acceptor in this beta-oxidation, further classifying this bacterium as an obligate aerobe.[15][17] Evidence has also shown that peroxides such as H2O2 can also serve as a terminal electron acceptor, with catalase activity needed for survival in vivo.[16] L. interrogans has only one glucose uptake system, known as the glucose sodium symporter.[18]

Genomics

The L. interrogans genome consists of two circular chromosomes composed of a total of almost 4.7 Mbp.[19] The larger chromosome has a total genome of 4.3 Mbp, and the smaller chromosome has a size of 350 Kbp. It has a G+C content of 35% and contains 3,400-3,700 protein-coding genes, depending on the strain.[11] The genes on the large chromosome encodes mostly housekeeping functions. Unlike most other bacteria, where the rRNA genes are clustered, in Leptospira the 16S, 23S, and 5S rRNA genes are scattered on the large chromosome.[11] Genes specifically encoding for long-chain fatty-acid usage, the TCA cycle, and electron transport chain have also been identified in L. interrogans. The detection of such genes confirms the use of oxidative phosphorylation as the primary metabolic pathway of L. interrogans. A large amount of genes related to eukaryotic cell invasion, cell attachment, and motility have been discovered. L. interrogans also has a complex set of genes associated with chemotaxis, more so than other pathogenic bacteria such as B. burgdorferi and T. palladium. Such genes able L. interrogans to be such a successful pathogen.[19]

To have the energy necessary for growth and to take over host functions, the bacterium employs methods such as oxidative stress.[20] Stress responses seen in L. interrogans include the up-regulation expression of genes encoding proteins such as chaperone proteins including clpA, heat shock proteins including GroEL, and endoflagellar proteins including flgA.[21]

Molecular pathogenesis

The loa22 gene has been classified as a virulence factor.[22]

LipL32 is the most abundant protein in L. interrogans. Although LipL32 binds to a number of extracellular matrix components in test tube experiments, there is doubt regarding where this protein is located. One study suggests that it is a subsurface membrane lipoprotein on the inner leaflet of the outer membrane.[23][24] Some outer membrane proteins, such as OmpL1, aid in the infection process of L. interrogans by allowing adherence to host cells's surface molecules.[25]

As L. interrogans is an obligate aerobe, reactive oxygen species (ROS) must be avoided during metabolism. The perRA and perRB genes encode peroxide responsive regulators, and these regulators promote host adaptation as they contain approximately 17 genes which aid in signaling.[26] L. interrogans also has a rather complex chemotaxis system compared to other pathogenic microbes, contributing to its effectiveness as a pathogen. Virulence is also related to the leptospiral LPS, which is known to uniquely activate macrophages in response to infection.[19]

The bacterial chaperone ClpB is a major driver in the overall virulence of L. interrogans, as it aids in survival inside the host, the control of stress responses, and the unique role of protein disaggregation.[20]

Environment

L. interrogans are host-associated bacteria, and most infections occur in tropical regions. In the host environment, L. interrogans are first found in the blood and subsequently moves on to infect several organs. In particular, L. interrogans cells survive and multiply at an optimal rate in the kidneys. The pathogen mostly spreads through the bodily fluids of infected animals.[17] Rats are the primary carrier of leptospirosis but do not present any symptoms, transmitting the pathogen through urine, which is able to persist in freshwater.[27] The pathogen can then enter the body of a new host through the skin and mucous membranes, as well as through the consumption of contaminated waters.[17] Leptospira often enter the body through open cuts and other wounds, though they are unable to pass through an intact skin barrier.[27] Infected wild and domestic animals can continue to excrete the bacteria into the environment for several years, and the bacteria can survive in soil and water for months at a time.[28]

Disease

For the disease, see Leptospirosis.

Humans

In humans, symptoms caused by L. interrogans are biphasic, icteric, or anicteric. The icteric form is also known as Weil's disease.[29] It has been shown in studies that L. interrogans may damage the endothelial cell lining of various vessels and organs, allowing them to leak and further spread the bacteria to other parts of the body.[30] Symptoms can appear anywhere between 2 and 4 weeks after exposure. Phase 1 of infection is anicteric, and symptoms include fever, chills, headache, muscle aches, vomiting and diarrhea. Roughly 90% of infectious cases in humans will only consist of this phase; however, it is possible for the disease to progress into phase 2, known as the icteric phase. Symptoms of the icteric phase include petechiae, hepatomegaly, jaundice, renal tubular damage, hemorrhages, and subsequent renal insufficiency.[29] Leptospirosis is treated with the antibiotics doxycycline and penicillin.[28]

There are more than 200 diverse pathogenic Leptospira serovars, making it challenging to develop an effective vaccine.[31] However, vaccines for the serovars known as Hardjo, Pomona, Canicola, Grippotyphosa and icterohaemorrhagiae have been developed. Unfortunately, these vaccines display suboptimal protection, need frequent booster doses, and are specific to certain serovars.[31]

Dogs

Leptospirosis in canines can be divided into the four categories of reproductive, icteric, hemorrhagic, and uremic. Reproductive leptospirosis results in the premature birth of offspring or abortion, and uremic leptospirosis is referred to as Stuttgart disease.[32] L. interrogans triggers a highly inflammatory response in infected dogs. This inflammatory response results in the high expression of tumor necrosis factor alpha, referred to as TNF-α, in the uterine tissue of infected dogs. Interleukin-1β and interleukin-6 also exhibit increased levels of expression upon infection. Furthermore, L. interrogans is proven to result in the down-regulation of extracellular matrix (ECM) mRNA and proteins. These factors are likely correlated with the high susceptibility of canines to leptospirosis.[32]

References

  1. ^ a b c Nakamura S (February 2022). "Motility of the Zoonotic Spirochete Leptospira: Insight into Association with Pathogenicity". Int J Mol Sci. 23 (3): 1859. doi:10.3390/ijms23031859. PMC 8837006. PMID 35163781.
  2. ^ a b c "Leptospirosis | CDC". www.cdc.gov. 2019-03-13. Retrieved 2022-11-13.
  3. ^ Ren SX, Fu G, Jiang XG, Zeng R, Miao YG, Xu H, Zhang YX, Xiong H, Lu G, Lu LF, Jiang HQ, Jia J, Tu YF, Jiang JX, Gu WY, Zhang YQ, Cai Z, Sheng HH, Yin HF, Zhang Y, Zhu GF, Wan M, Huang HL, Qian Z, Wang SY, Ma W, Yao ZJ, Shen Y, Qiang BQ, Xia QC, Guo XK, Danchin A, Saint Girons I, Somerville RL, Wen YM, Shi MH, Chen Z, Xu JG, Zhao GP (April 2003). "Unique physiological and pathogenic features of Leptospira interrogans revealed by whole-genome sequencing". Nature. 422 (6934): 888–93. Bibcode:2003Natur.422..888R. doi:10.1038/nature01597. PMID 12712204. S2CID 4415685.
  4. ^ "Risk of Exposure | Risk of Exposure | Leptospirosis | CDC". www.cdc.gov. 2018-11-07. Retrieved 2022-10-16.
  5. ^ Wang S, Stobart Gallagher MA, Dunn N (2021). "Leptospirosis". StatPearls. Treasure Island (FL): StatPearls Publishing. PMID 28722888.
  6. ^ Behera, Sujit Kumar; Sabarinath, Thankappan; Ganesh, Balasubramanian; Mishra, Prasanta Kumar K.; Niloofa, Roshan; Senthilkumar, Kuppusamy; Verma, Med Ram; Hota, Abhishek; Chandrasekar, Shanmugam; Deneke, Yosef; Kumar, Ashok; Nagarajan, Muruganandam; Das, Deepanker; Khatua, Sasmita; Sahu, Radhakrishna (2022-06-13). "Diagnosis of Human Leptospirosis: Comparison of Microscopic Agglutination Test with Recombinant LigA/B Antigen-Based In-House IgM Dot ELISA Dipstick Test and Latex Agglutination Test Using Bayesian Latent Class Model and MAT as Gold Standard". Diagnostics. 12 (6): 1455. doi:10.3390/diagnostics12061455. ISSN 2075-4418. PMC 9221883. PMID 35741265.
  7. ^ "Treatment | Leptospirosis | CDC". www.cdc.gov. 2018-11-02. Retrieved 2023-10-13.
  8. ^ "Leptospirosis - Infectious Diseases". Merck Manuals Professional Edition. Retrieved 2023-10-13.
  9. ^ Qu, Jiaxin. Sequencing and comparative genomics of Leptospira interrogans serovar pomona and Leptospira kirschneri serovar grippotyphosa. The University of Oklahoma, 2007.
  10. ^ Evangelista, Karen V, and Jenifer Coburn. “Leptospira as an emerging pathogen: a review of its biology, pathogenesis and host immune responses.” Future microbiology vol. 5,9 (2010): 1413-25. doi:10.2217/fmb.10.102
  11. ^ a b c Picardeau M (2015). "Genomics, proteomics, and genetics of leptospira". Current Topics in Microbiology and Immunology. 387: 43–63. doi:10.1007/978-3-662-45059-8_4. ISBN 978-3-662-45058-1. PMID 25388132.
  12. ^ a b Hines MT (2014). "Chapter 32 - Leptospirosis". In Sellon DC, Long MT (eds.). Equine Infectious Diseases (2nd ed.). W.B. Saunders. pp. 302–311. doi:10.1016/B978-1-4557-0891-8.00032-4. ISBN 978-1-4557-0891-8.
  13. ^ a b Levett PN (April 2001). "Leptospirosis". Clinical Microbiology Reviews. 14 (2): 296–326. doi:10.1128/CMR.14.2.296-326.2001. PMC 88975. PMID 11292640.
  14. ^ Koizumi N, Watanabe H (2009). "Leptospirosis". Vaccines for Biodefense and Emerging and Neglected Diseases. Academic Press. pp. 1291–1308. doi:10.1016/B978-0-12-369408-9.00064-0. ISBN 978-0-12-369408-9.
  15. ^ a b Evangelista KV, Coburn J (September 2010). "Leptospira as an emerging pathogen: a review of its biology, pathogenesis and host immune responses". Future Microbiology. 5 (9): 1413–1425. doi:10.2217/fmb.10.102. PMC 3037011. PMID 20860485.
  16. ^ a b c d e Cameron CE (2015). Alder B (ed.). "Leptospiral structure, physiology, and metabolism". Current Topics in Microbiology and Immunology. 387. Berlin, Heidelberg: Springer: 21–41. doi:10.1007/978-3-662-45059-8_3. ISBN 978-3-662-45059-8. PMID 25388131.
  17. ^ a b c Johnson RC, Leptospira (1996). "Leptospira". In Baron S (ed.). Medical Microbiology (4th ed.). Galveston (TX): University of Texas Medical Branch at Galveston. ISBN 978-0-9631172-1-2. PMID 21413339.
  18. ^ Nascimento AL, Ko AI, Martins EA, Monteiro-Vitorello CB, Ho PL, Haake DA, et al. (April 2004). "Comparative genomics of two Leptospira interrogans serovars reveals novel insights into physiology and pathogenesis". Journal of Bacteriology. 186 (7): 2164–2172. doi:10.1128/JB.186.7.2164-2172.2004. PMC 374407. PMID 15028702.
  19. ^ a b c Ren, Shuang-Xi; Fu, Gang; Jiang, Xiu-Gao; Zeng, Rong; Miao, You-Gang; Xu, Hai; Zhang, Yi-Xuan; Xiong, Hui; Lu, Gang; Lu, Ling-Feng; Jiang, Hong-Quan; Jia, Jia; Tu, Yue-Feng; Jiang, Ju-Xing; Gu, Wen-Yi (April 2003). "Unique physiological and pathogenic features of Leptospira interrogans revealed by whole-genome sequencing". Nature. 422 (6934): 888–893. Bibcode:2003Natur.422..888R. doi:10.1038/nature01597. ISSN 1476-4687. PMID 12712204. S2CID 4415685.
  20. ^ a b Kędzierska-Mieszkowska S, Arent Z (September 2020). "AAA+ Molecular Chaperone ClpB in Leptospira interrogans: Its Role and Significance in Leptospiral Virulence and Pathogenesis of Leptospirosis". International Journal of Molecular Sciences. 21 (18): 6645. doi:10.3390/ijms21186645. PMC 7555560. PMID 32932775.
  21. ^ Lo, Miranda; Bulach, Dieter M.; Powell, David R.; Haake, David A.; Matsunaga, James; Paustian, Michael L.; Zuerner, Richard L.; Adler, Ben (2006). "Effects of Temperature on Gene Expression Patterns in Leptospira interrogans Serovar Lai as Assessed by Whole-Genome Microarrays". Infection and Immunity. 74 (10): 5848–5859. doi:10.1128/IAI.00755-06. ISSN 0019-9567. PMC 1594916. PMID 16988264.
  22. ^ Verma V, Kala D, Gupta S, Kumar H, Kaushal A, Kuča K, et al. (April 2021). "Leptospira interrogans Outer Membrane Protein-Based Nanohybrid Sensor for the Diagnosis of Leptospirosis". Sensors. 21 (7): 2552. Bibcode:2021Senso..21.2552V. doi:10.3390/s21072552. PMC 8038715. PMID 33917354.
  23. ^ Pinne M, Haake DA (2013-01-08). Hartskeerl RA (ed.). "LipL32 Is a Subsurface Lipoprotein of Leptospira interrogans: presentation of new data and reevaluation of previous studies". PLOS ONE. 8 (1): e51025. Bibcode:2013PLoSO...851025P. doi:10.1371/journal.pone.0051025. PMC 3544172. PMID 23323152.
  24. ^ Murray GL (2015). "The molecular basis of leptospiral pathogenesis". Current Topics in Microbiology and Immunology. 387: 139–85. doi:10.1007/978-3-662-45059-8_7. ISBN 978-3-662-45058-1. PMID 25388135.
  25. ^ Robbins GT, Hahn BL, Evangelista KV, Padmore L, Aranda PS, Coburn J (April 2015). "Evaluation of cell binding activities of Leptospira ECM adhesins". PLOS Neglected Tropical Diseases. 9 (4): e0003712. doi:10.1371/journal.pntd.0003712. PMC 4397020. PMID 25875373.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  26. ^ Grassmann AA, Zavala-Alvarado C, Bettin EB, Picardeau M, Benaroudj N, Caimano MJ (December 2021). "The FUR-like regulators PerRA and PerRB integrate a complex regulatory network that promotes mammalian host-adaptation and virulence of Leptospira interrogans". PLOS Pathogens. 17 (12): e1009078. doi:10.1371/journal.ppat.1009078. PMC 8638967. PMID 34855918.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  27. ^ a b Eshghi A, Pappalardo E, Hester S, Thomas B, Pretre G, Picardeau M (August 2015). "Pathogenic Leptospira interrogans exoproteins are primarily involved in heterotrophic processes". Infection and Immunity. 83 (8): 3061–3073. doi:10.1128/IAI.00427-15. PMC 4496612. PMID 25987703.
  28. ^ a b "Leptospirosis | CDC". www.cdc.gov. 2019-03-13. Retrieved 2021-11-23.
  29. ^ a b Wang S, Stobart Gallagher MA, Dunn N (2021). "Leptospirosis". StatPearls. Treasure Island (FL): StatPearls Publishing. PMID 28722888.
  30. ^ Sato, Hiromi; Coburn, Jenifer (2017-07-27). "Leptospira interrogans causes quantitative and morphological disturbances in adherens junctions and other biological groups of proteins in human endothelial cells". PLOS Neglected Tropical Diseases. 11 (7): e0005830. doi:10.1371/journal.pntd.0005830. ISSN 1935-2735. PMC 5549773. PMID 28750011.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  31. ^ a b Wang Z, Jin L, Wegrzyn A (December 2007). "Leptospirosis vaccines". Microbial Cell Factories. 6: 39. doi:10.1186/1475-2859-6-39. PMC 2231387. PMID 18072968.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  32. ^ a b Wang W, Gao X, Guo M, Zhang W, Song X, Wang T, et al. (October 2014). "Leptospira interrogans induces uterine inflammatory responses and abnormal expression of extracellular matrix proteins in dogs". Microbial Pathogenesis. 75: 1–6. doi:10.1016/j.micpath.2014.07.011. PMID 25153777.
Retrieved from "https://en.wikipedia.org/w/index.php?title=Leptospira_interrogans&oldid=1179873170"