Leptospirosis

Leptospirosis
Classification and external resources

Leptospirose magnified 200 times with dark-field microscope
ICD-10 A27.
DiseasesDB 7403
MedlinePlus 001376
eMedicine med/1283 emerg/856 ped/1298
MeSH C01.252.400.511

Leptospirosis (also known as Weil's disease, Weil's syndrome, canicola fever, canefield fever, nanukayami fever, 7-day fever, Rat Catcher's Yellows, Fort Bragg fever, and Pretibial fever[1]:290) is a bacterial zoonotic disease caused by spirochaetes of the genus Leptospira that affects humans and a wide range of animals, including mammals, birds, amphibians, and reptiles. The disease was first described by Adolf Weil in 1886 when he reported an "acute infectious disease with enlargement of spleen, jaundice and nephritis". Leptospira was first observed in 1907 from a post mortem renal tissue slice.[2] In 1908, Inada and Ito first identified it as the causative organism [3]and in 1916 noted its presence in rats.[4]

Though being recognised among the world's most common zoonoses, leptospirosis is a relatively rare bacterial infection in humans. The infection is commonly transmitted to humans by allowing water that has been contaminated by animal urine to come in contact with unhealed breaks in the skin, eyes or with the mucous membranes. Outside of tropical areas, leptospirosis cases have a relatively distinct seasonality with most of them occurring August–September/February–March.

Contents

Causes

Scanning electron micrograph of a number of Leptospira sp. bacteria atop a 0.1 µm polycarbonate filter

Leptospirosis is caused by a spirochaete bacterium called Leptospira spp. that has at least 5 serovars of importance in the United States and Canada causing disease in dogs (Icterohaemorrhagiae, Canicola, Pomona, Grippotyphosa, and Bratislava)[5]. There are other (less common) infectious strains. Genetically different leptospira organisms may be identical serologically and vice versa. Hence, an argument exists on the basis of strain identification. The traditional serologic system is seemingly more useful from a diagnostic and epidemiologic standpoint at the moment (which may change with further development and spread of technologies like PCR).

Leptospirosis is transmitted by the urine of an infected animal and is contagious as long as it is still moist. Although rats, mice and voles are important primary hosts, a wide range of other mammals including dogs, deer, rabbits, hedgehogs, cows, sheep, raccoons, possums, skunks, and certain marine mammals are able to carry and transmit the disease as secondary hosts. Dogs may lick the urine of an infected animal off the grass or soil, or drink from an infected puddle. There have been reports of "house dogs" contracting leptospirosis apparently from licking the urine of infected mice that entered the house. The type of habitats most likely to carry infective bacteria are muddy riverbanks, ditches, gullies, and muddy livestock rearing areas where there is regular passage of either wild or farm mammals. There is a direct correlation between the amount of rainfall and the incidence of leptospirosis, making it seasonal in temperate climates and year-round in tropical climates.

Leptospirosis is also transmitted by the semen of infected animals.[6] Slaughterhouse workers can contract the disease through contact with infected blood or body fluids.

Humans become infected through contact with water, food, or soil containing urine from these infected animals. This may happen by swallowing contaminated food or water, or through skin contact. The disease is not known to be spread from person to person and cases of bacterial dissemination in convalescence are extremely rare in humans. Leptospirosis is common among water-sport enthusiasts in specific areas as prolonged immersion in water is known to promote the entry of the bacteria. Surfers and whitewater paddlers [7] are at especially high risk in areas that have been shown to contain the bacteria, and can contract the disease by swallowing contaminated water, splashing contaminated water into their eyes or nose, or exposing open wounds to infected water.[8] Occupations at risk include veterinarians, slaughterhouse workers, farmers, sewer workers, and people working on derelict buildings, rowers are also sometimes known to contact the disease.[5]

Symptoms

Leptospiral infection in humans causes a range of symptoms, and some infected persons may have no symptoms at all. Leptospirosis is a biphasic disease that begins with flu-like symptoms (fever, chills, myalgias, intense headache). The first phase resolves, and the patient is briefly asymptomatic until the second phase begins. This is characterized by meningitis, liver damage (causing jaundice), and renal failure. The infection is often wrongly diagnosed due to the wide range of symptoms. This leads to a lower registered number of cases than actually exist. Symptoms of leptospirosis include high fever, severe headache, chills, muscle aches, and vomiting, and may include jaundice, red eyes, abdominal pain, diarrhea, and rash. The symptoms in humans appear after a 4–14 day incubation period.

The incubation period (time of exposure to first symptoms) in animals is anywhere from 2 to 20 days. In dogs the liver and kidney are most commonly damaged by leptospirosis. Vasculitis can occur, causing edema and potentially disseminated intravascular coagulation (DIC). Myocarditis, pericarditis, meningitis, and uveitis are also possible sequelae. [5] One should strongly suspect leptospirosis and include it as part of a differential diagnosis if the sclerae of the dog's eyes appear jaundiced (even slightly yellow). The absence of jaundice does not eliminate the possibility of leptospirosis, and its presence could indicate hepatitis or other liver pathology rather than leptospirosis. Vomiting, fever, failure to eat, reduced urine output, unusually dark or brown urine, and lethargy are also indications of the disease.

Complications

Complications include meningitis, extreme fatigue, hearing loss, respiratory distress, azotemia, and renal interstitial tubular necrosis, which results in renal failure and often liver failure (the severe form of this disease is known as Weil's disease, though it is sometimes named Weil Syndrome[9]). Cardiovascular problems are also possible.

Diagnosis

Kidney tissue, using a silver staining technique, revealing the presence of Leptospira bacteria

On infection the microorganism can be found in blood for the first 7 to 10 days (invoking serologically identifiable reactions) and then moving to the kidneys. After 7 to 10 days the microorganism can be found in fresh urine. Hence, early diagnostic efforts include testing a serum or blood sample serologically with a panel of different strains. It is also possible to culture the microorganism from blood, serum, fresh urine and possibly fresh kidney biopsy. Kidney function tests (Blood Urea Nitrogen and creatinine) as well as blood tests for liver functions are performed. The latter reveal a moderate elevation of transaminases. Brief elevations of aspartate aminotransferase (AST), alanine aminotransferase (ALT), and gamma-glutamyltransferase (GGT) levels are relatively mild. These levels may be normal, even in children with jaundice. Diagnosis of leptospirosis is confirmed with tests such as Enzyme-Linked Immunosorbent Assay (ELISA) and PCR. Serological testing, the MAT (microscopic agglutination test), is considered the gold standard in diagnosing leptospirosis. As a large panel of different leptospira need to be subcultured frequently, which is both laborious and expensive, it is underused, mainly in developing countries.

Differential diagnosis list for leptospirosis is very large due to diverse symptomatics. For forms with middle to high severity, the list includes dengue fever and other hemorrhagic fevers, hepatitis of various etiologies, viral meningitis, malaria and typhoid fever. Light forms should be distinguished from influenza and other related viral diseases. Specific tests are a must for proper diagnosis of leptospirosis. Under circumstances of limited access (e.g., developing countries) to specific diagnostic means, close attention must be paid to anamnesis of the patient. Factors like certain dwelling areas, seasonality, contact with stagnant contaminated water (Bathing swimming, working on flooded meadows, etc) and/or rodents in the medical history support the leptospirosis hypothesis and serve as indications for specific tests (if available).

Leptospira can be cultured in Ellinghausen-McCullough-Johnson-Harris medium, which is incubated at 28 to 30 °C.[10] The median time to positivity is three weeks with a maximum of 3 months. This makes culture techniques useless for diagnostic purposes, but is commonly used in research.

Prevention

Doxycycline may be used to prevent infection in adventure travelers to high risk areas.[11]

Treatment

Leptospirosis treatment is a relatively complicated process comprising two main components: suppressing the causative agent and fighting possible complications. Aetiotropic drugs are antibiotics, such as cefotaxime, doxycycline, penicillin, ampicillin, and amoxicillin (doxycycline can also be used as a prophylaxis). There are no human vaccines; animal vaccines are only for a few strains, and are only effective for a few months. Human therapeutic dosage of drugs is as follows: doxycycline 100 mg orally every 12 hours for 1 week or penicillin 1–1.5 MU every 4 hours for 1 week. Doxycycline 200–250 mg once a week is administered as a prophylaxis. In dogs, penicillin is most commonly used to end the leptospiremic phase (infection of the blood), and doxycycline is used to eliminate the carrier state.

Supportive therapy measures (esp. in severe cases) include detoxification and normalization of the hydro-electrolytic balance. Glucose and salt solution infusions may be administered; dialysis is used in serious cases. Elevations of serum potassium are common and if the potassium level gets too high special measures must be taken. Serum phosphorus levels may likewise increase to unacceptable levels due to renal failure. Treatment for hyperphosphatemia consists of treating the underlying disease, dialysis where appropriate, or oral administration of calcium carbonate, but not without first checking the serum calcium levels (these two levels are related). Corticosteroids administration in gradually reduced doses (e.g., prednisolone starting from 30–60 mg) during 7–10 days is recommended by some specialists in cases of severe haemorrhagic effects. Organ specific care and treatment are essential in cases of renal, liver or heart involvement.

Epidemiology

Annual rates of infection vary from 0.02 per 100,000 in temperate climates to 10 to 100 per 100,000 in tropical climates.[12]

History

Leptospirosis was postulated as the cause of an epidemic among native Americans along the coast of present-day Massachusetts that occurred immediately before the arrival of the Pilgrims in 1620 and wiped out most of the native population.[13] Earlier proposals included plague, yellow fever, smallpox, influenza, chickenpox, typhus, typhoid fever, trichinellosis, meningitis, and syndemic infection of hepatitis B virus with the delta agent.[14][15][16][17] None are as consistent with all the evidence as leptospirosis. While the disease may have been brought to the New World by Europeans, its spread was also influenced by the high-risk quotidian activities of the Native Americans. The leptospirosis hypothesis is supported by the occurrence of modern outbreaks identified as severe leptospirosis, some accompanied by high mortality rates (the Andaman Islands in the late 1980s, the Philippines in 2009, Ireland in 2010).[18][19][20]

The Indian lifestyle exposed them to the leptospiral life cycle.

The cause of this epidemic has been a mystery, while other outbreaks in the same time frame are fairly well established. The epidemic is considered a pivotal event in American history since the failure of the Plymouth Bay colony might have meant the failure of British colonization in North American [21] A noted historian has said that the epidemic was the most important event in American history between the discovery of America by Columbus and the signing of the Declaration of Independence.

Before Weil's characterization in 1886, the disease known as infectious jaundice was very likely the same as Weil's disease, or severe icteric leptospirosis. During the Egyptian campaign, Napoleon's army suffered from what was probably infectious jaundice.[22] Infectious jaundice occurred among troops during the American Civil War[23] It was also reported among troops at Gallipoli and other battles of World War I, where the sodden conditions of trench warfare favored infection. Terms used in early 20th century descriptions of leptospirosis include the pseudo-dengue of Java, seven-day fever, autumn fever, Akiyama disease and marsh or swamp fever. L icterohaemorrhagieae was identified as the causative agent in Pre-World War II outbreaks in Japan, which were characterized by jaundice and a high mortality rate.

References

  1. ↑ James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 0-7216-2921-0. 
  2. ↑ Stimson AM (1907). "Note on an organism found in yellow-fever tissue." Public Health Reports 22:541.
  3. ↑ Inada R, Ito Y. A report of the discovery of the causal organism (a new species of spirocheta) of Weil's disease. Tokyo Ijishinshi. 1908;1915:351-60.
  4. ↑ Inanda R, Ido Y, Hoke R, Kaneko R, Ito H. The Etiology, Mode of Infection and Specific Therapy of Weil's Disease. J Exper Med 23;377:1916.
  5. ↑ 5.0 5.1 5.2 Langston CE, Heuter KJ (July 2003). "Leptospirosis. A re-emerging zoonotic disease". The Veterinary clinics of North America. Small animal practice 33 (4): 791–807. doi:10.1016/S0195-5616(03)00026-3. PMID 12910744. 
  6. ↑ Kiktenko VS; Balashov, NG; Rodina, VN (1976). "Leptospirosis infection through insemination of animals". J Hyg Epidemiol Microbiol Immunol. 21 (2): 207–213. PMID 987112. 
  7. ↑ Kayaking as a risk factor for leptospirosis. Shaw RD, Mo Med. 1992; 89(6):354-7 (ISSN: 0026-6620)
  8. ↑ Seven Surfing Sicknesses, .
  9. ↑ Weil syndrome definition - Medical Dictionary definitions of popular medical terms easily defined on MedTerms
  10. ↑ Rule PL, Alexander AD (1986). "Gellan gum as a substitute for agar in leptospiral media". J Clin Microbiol 23 (3): 500–504. PMID 3754265. 
  11. ↑ Pavli A, Maltezou HC (2008). "Travel-acquired leptospirosis". J Travel Med 15 (6): 447–53. doi:10.1111/j.1708-8305.2008.00257.x. PMID 19090801. 
  12. ↑ Pavli A, Maltezou HC (2008). "Travel-acquired leptospirosis". J Travel Med 15 (6): 447–53. doi:10.1111/j.1708-8305.2008.00257.x. PMID 19090801. 
  13. ↑ Marr JS, Cathey JT. New hypothesis for cause of an epidemic among Native Americans, New England, 1616–1619. Emerg Infect Dis [serial on the Internet]. 2010 Feb. http://www.cdc.gov/EID/content/16/2/281.htm DOI: 10.3201/edi1602.090276
  14. ↑ Webster N. A brief history of epidemic and pestilential diseases. Hartford (CT): Hudson and Goodwin; 1799
  15. ↑ Williams H. The epidemic of the Indians of New England, 1616-1620, with remarks on Native American infections. John Hopkins Hospital Bulletin. 190920:340-9.
  16. ↑ Bratton TL. The identity of the New England Indian epidemic of 1616-19. Bull Hist Med. 1988;62:351-83.
  17. ↑ Speiss A, Speiss BD. New England pandemic of 1616-1622. cause and archeological implication. Man in the Northeast. 1987;34:71-83.
  18. ↑ Vijayachari P, Sugunan AP, Sharma S, Roy S, Natarajaseenivasan K, Sehgal SC. Leptospirosis in the Andaman Islands, India. Trans R Soc Trop Med Hyg. 2008;102:117-22. DOI: 10.1016/j.trstmh.2007.08.012
  19. ↑ ProMED-mail. Leptospirosis - Philippines (02): background. ProMED-mail 2009; 18 Oct: 20091018.3579. <http://www.promedmail.org>. Accessed 16 January 2010.
  20. ↑ ProMED-mail. Leptospirosis, fatal - Ireland (02): background. ProMED-mail 2010; 06 Jan: 20100106.0055. <http://www.promedmail.org>. Accessed 16 January 2010.
  21. ↑ 1616: The Counterfactual
  22. ↑ Strong RP. Stitt's Diagnosis, Prevention and Treatment of Tropical Diseases. Seventh Edition. Blakiston: York PA; 1944.
  23. ↑ Neill M. The problem of acute infectious jaundice in the United States. Public Health Rep. 1918;33:717-26.

External links

Further reading

Infectious diseases · Bacterial diseases: BV4 non-proteobacterial G- (primarily A00-A79, 001-041,080-109)
Spirochaete
Spirochaetaceae
Treponema
Treponema pallidum (Syphilis/Bejel, Yaws) · Treponema carateum (Pinta) · Treponema denticola
Borrelia

Borrelia burgdorferi/Borrelia afzelii (Lyme disease, Erythema chronicum migrans, Neuroborreliosis)

Borrelia recurrentis (Louse borne relapsing fever) · Borrelia hermsii/Borrelia duttoni/Borrelia parkeri (Tick borne relapsing fever)
Leptospiraceae
Leptospira
Leptospira interrogans (Leptospirosis)
Spirillaceae
Spirillum
Spirillum minus (Rat-bite fever/Sodoku)
Chlamydiaceae
Chlamydophila
Chlamydophila psittaci (Psittacosis) · Chlamydophila pneumoniae
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Chlamydia trachomatis (Chlamydia, Lymphogranuloma venereum, Trachoma)
Bacteroidetes
Bacteroides fragilis · Bacteroides forsythus · Capnocytophaga canimorsus · Porphyromonas gingivalis · Prevotella intermedia
Fusobacteria

Fusobacterium necrophorum (Lemierre's syndrome) · Fusobacterium nucleatum · Fusobacterium polymorphum

Streptobacillus moniliformis (Rat-bite fever/Haverhill fever)

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