Leptospirosis

Veterinary Client Brochure

Educate clients with the brochure Leptospirosis in Dogs and Cats, also available in Spanish (Leptospirosis en Perros y Gatos).

Leptospirosis is a disease caused by infection with Leptospira bacteria. These bacteria can be found worldwide in soil and water. There are many strains of Leptospira
bacteria that can cause disease. Leptospirosis is a zoonotic disease, which means it can be spread from animals to people. Infection in people can cause flu-like
symptoms and can cause liver or kidney disease. In the United States, most cases of human leptospirosis result from recreational activities involving water. Infection
resulting from contact with an infected pet is much less common, but it is possible.

Leptospirosis is more common in areas with warm climates and high annual rainfall but it can occur anywhere.

Risk factors for leptospirosis

Dogs are most commonly affected. Leptospirosis in cats is rare and appears to be mild although very little is known about the disease in this species. Common risk factors
for leptospirosis in dogs residing in the United States include exposure to or drinking from rivers, lakes or streams; roaming on rural properties (because of exposure to
potentially infected wildlife, farm animals, or water sources); exposure to wild animal or farm animal species, even if in the backyard; and contact with rodents or other
dogs.

Dogs can become infected and develop leptospirosis if their mucous membranes (or skin with any wound, such as a cut or scrape) come into contact with infected urine,
urine-contaminated soil, water, food or bedding; through a bite from an infected animal; by eating infected tissues or carcasses; and rarely, through breeding. It can also be
passed through the placenta from the mother dog to the puppies.

Signs of leptospirosis
The signs of leptospirosis in dogs vary. Some infected dogs do not show any signs of illness, some have a mild and transient illness and recover spontaneously, while
others develop severe illness and death.

Signs of leptospirosis may include fever, shivering, muscle tenderness, reluctance to move, increased thirst, changes in the frequency or amount of urination, dehydration,
vomiting, diarrhea, loss of appetite, lethargy, jaundice (yellowing of the skin and mucous membranes), or painful inflammation within the eyes. The disease can cause
kidney failure with or without liver failure. Dogs may occasionally develop severe lung disease and have difficulty breathing. Leptospirosis can cause bleeding disorders,
which can lead to blood-tinged vomit, urine, stool or saliva; nosebleeds; and pinpoint red spots (which may be visible on the gums and other mucous membranes or on
light-colored skin). Affected dogs can also develop swollen legs (from fluid accumulation) or accumulate excess fluid in their chest or abdomen.

Leptospirosis may be suspected based on the exposure history and signs shown by the dog, but many of these signs can also be seen with other diseases. In addition to a
physical examination, your veterinarian may recommend a number of other tests such as blood tests, urine tests, radiographs (x-rays), and an ultrasound examination.

Treatment and prevention

Leptospirosis is generally treated with antibiotics and supportive care. When treated early and aggressively, the chances for recovery are good but there is still a risk of
permanent residual kidney or liver damage.

Currently available vaccines effectively prevent leptospirosis and protect dogs for at least 12 months. Annual vaccination is recommended for at-risk dogs. Reducing your
dog’s exposure to possible sources of the Leptospira bacteria can reduce its chances of infection.

Although an infected pet dog presents a low risk of infection for you and your family, there is still some risk. If your dog has been diagnosed with leptospirosis, take the
following precautions to protect yourself:

 Administer antibiotics as prescribed by your veterinarian;

 Avoid contact with your dog’s urine;

 If your dog urinates in your home, quickly clean the area with a household disinfectant and wear gloves to avoid skin contact with the urine;

 Encourage your dog to urinate away from standing water or areas where people or other animals will have access;

 Wash your hands after handling your pet.

Leptospirosis
From Wikipedia, the free encyclopedia

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Leptospirosis
Other names Rat fever,[1] field fever,[2] rat catcher's yellows,
[3]
pretibial fever[4]

Leptospira magnified 200-fold with a dark-field microscope

Specialty Infectious disease

Symptoms None, headaches, muscle pains, fevers[5]

Complications Bleeding from the lungs, meningitis, kidney

failure[5][6]

Usual onset 7–12 days[7]

Causes Leptospira typically spread by rodents[5][8]

 Risk factors Exposure to infected animals or contaminated

water[9]

Diagnostic method Testing blood for antibodies against the

bacterium or its DNA[10]

Differential Malaria, enteric fever, rickettsiosis, dengue[11]

diagnosis

Treatment Doxycycline, penicillin, ceftriaxone[5]

Frequency ~8.5 million people per year[12]

Deaths 58,900 per year[13]

Leptospirosis is an infection caused by corkscrew-shaped bacteria called Leptospira.[5] Signs and symptoms can range from none to mild such
as headaches, muscle pains, and fevers to severe with bleeding from the lungs or meningitis.[5][6] If the infection causes the person to turn yellow,
have kidney failure and bleeding, it is then known as Weil's disease.[6] If it also causes bleeding into the lungs then it is known as severe
pulmonary haemorrhage syndrome.[6]
Up to 10 different genetic types of Leptospira may cause disease in humans.[14] It is transmitted by both wild and domestic animals. [6] The most
common animals that spread the disease are rodents.[8] It is often transmitted by animal urine or by water or soil containing animal urine coming
into contact with breaks in the skin, eyes, mouth, or nose.[5][15] In the developing world the disease most commonly occurs in farmers and low-
income people who live in cities.[6] In the developed world it most commonly occurs in those involved in outdoor activities in warm and wet areas of
the world.[5] Diagnosis is typically by looking for antibodies against the bacterium or finding its DNA in the blood.[10]
Efforts to prevent the disease include protective equipment to prevent contact when working with potentially infected animals, washing after this
contact, and reducing rodents in areas where people live and work. [5] The antibiotic doxycycline, when used in an effort to prevent infection among
travelers, is of unclear benefit.[5] Vaccines for animals exist for certain type of Leptospira which may decrease the risk of spread to humans.
[5]
Treatment if infected is with antibiotics such as: doxycycline, penicillin, or ceftriaxone.[5] Weil's disease and severe pulmonary haemorrhage
syndrome result in death rates greater than 10% and 50%, respectively, even with treatment. [6]
It is estimated that seven to ten million people are infected by leptospirosis per year. [12] This results in about 58,900 deaths per year.[13] The disease
is most common in tropical areas of the world but may occur anywhere. [5] Outbreaks may occur in slums of the developing world.[6] The disease was
 first described by physician Adolf Weil in 1886 in Germany.[5][16] Animals which are infected may have no symptoms, mild symptoms, or severe
symptoms.[17] Symptoms may vary by the type of animal. [17] In some animals Leptospira live in the reproductive tract, leading to transmission during
mating.[18]

Contents

 1Signs and symptoms

 2Cause
o 2.1Bacteria

o 2.2Transmission

 3Pathogenesis

 4Diagnosis

 5Prevention

 6Treatment

 7Prognosis

 8Epidemiology

 9History

 10Other animals

 11References

 12External links
Signs and symptoms[edit]

Jaundice, one of the features in leptospirosis.

The symptoms appear after an incubation period of 7–12 days.[7] However, the incubation period can vary from 6 days to 29 days.[19] Leptospirosis
is a biphasic disease.[20] The first phase (acute or septic phase) ends after 3–7 days of illness. [7] The second phase (immune phase) starts with the
resolution of symptoms and appearance of antibodies. [21] Ninety percent of cases of the disease are mild leptospirosis. The rest experience severe
disease, which develops during the second stage or occurs as a single progressive illness. [22]
Leptospiral infection in humans causes a range of symptoms, and some infected persons may have no symptoms at all. The disease begins
suddenly with fever accompanied by chills, intense headache, severe muscle aches, abdominal pain, and occasionally a skin rash.[20] The
headache in leptospirosis is characteristically located at the bilateral temporal or frontal regions with throbbing pain. The person could also have
pain behind the eyes and sensitivity to light.[19] Muscle pain usually involves the calf muscle and the lower back.[19] The most characteristic feature of
leptospirosis is the conjunctival suffusion (conjunctivitis without exudate) which is not commonly found in other febrile illnesses. Other
characteristic findings on the eye include subconjunctival bleeding and jaundice.[19] Rash is rarely found in leptospirosis. When rash is found, other
alternative diagnoses such as Dengue fever and Chikungunya fever should be considered.[19] Dry cough is observed in 20% to 57% of people with
leptospirosis. Thus, this clinical feature can mislead a doctor to diagnose the disease as respiratory illness. Additionally, gastrointestinal symptoms
such as nausea, vomiting, abdominal pain, and diarrhea frequently occurs. Vomiting and diarrhea may contribute to dehydration in conjunction with
kidney failure due to excessive urine output. [19] The abdominal pain can be due to acalculous cholecystitis or inflammation of the pancreas.
[19]
Rarely, the lymph nodes, liver, and spleen may be enlarged and palpable.[21]
The disappearance of symptoms coincides with the appearance of antibodies against Leptospira and the disappearance of bacteria from the
bloodstream. The patient is asymptomatic for 3–4 days until the second phase begins with another episode of fever. [20] The immune phase can last
from 4 to 30 days. It can be anything from brain to kidney complications. [23] The hallmark of the second phase is meningitis (inflammation of the
membranes covering the brain).[24] Signs and symptoms of meningitis include severe headache and neck stiffness. In 5% to 10% of those infected
with jaundice, the disease can be rapidly progressive to multiorgan failure. [25]
Severe leptospirosis can cause liver, kidney, lungs, and brain damage. For those with signs of inflammation of membranes covering the brain and
the brain itself, altered level of consciousness can occur. A variety of neurological complications can occur such as paralysis of half of the
body, complete inflammation of whole section of spinal cord, and muscle weakness due to immune damage of the nerves supplying the muscles.
[19]
Signs of bleeding such as non-traumatic bruises at 1 mm, non-traumatic bruises more than 1 cm, nose bleeding, blackish stools due to bleeding
in stomach, vomiting blood and bleeding from the lungs can also be found. Prolongation of prothrombin time in coagulation testing is associated
with severe bleeding manifestation. However, low platelet count is not associated with severe bleeding.[19] In less than 5% of those infected,
pulmonary haemorrhage can occur at the 4th to 6th day of the illness and can be rapidly fatal. [25] Leptospira causes alveolar haemorrhage (bleeding
into the alveoli of the lungs) and massive coughing up blood. This causes acute respiratory distress syndrome. This feature increases the risk of
death to more than 50%.[19] Rarely, inflammation of heart muscles, inflammation of membranes covering the heart, abnormalities in pacemaker of
the heart and abnormal heart rhythms may occur.[21] The classic form of severe leptospirosis is known as Weil's disease, which is characterized by
liver damage (causing jaundice), kidney failure, and bleeding.[26]

Cause[edit]
Bacteria[edit]

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

Leptospirosis belongs to the genus Leptospira which are aerobic,[21] right-handed helical[14] bacteria ; sized at 6 to 20 micrometers. Hooked ends of
this bacterium give it a "question mark" shape.[27] Like Gram-negative bacteria, Leptospira have an outer membrane studded
with lipopolysaccharide (LPS) on the surface, an inner membrane, and a layer of peptidoglycan. However, unlike Gram-negative bacteria, the
peptidoglycan layer in Leptospira lies closer to the inner membrane than the outer membrane. This results in a fluid outer membrane loosely
associated with the cell wall.[28] In addition, Leptospira have two flagella located in the periplasm.[27] Chemoreceptors at the poles of the bacteria
sense various substrates and change the direction of the bacteria's movement. [14] The bacteria are traditionally visualised using dark-field
microscopy with silver staining or immunofluorescence staining.[29]
A total of 22 species of Leptospira have been identified.[14] The species can be divided into three clades based on their 16S rRNA sequence. The
first is the "pathogens" clade comprising the eight species that can cause severe disease in humans: L. alexanderi, L. borgpetersenii, L.
interrogans, L. kirschneri, L. mayottensis, L. noguchii, L. santarosai, and L. weilii, along with two related species that are not known to cause
disease in any animal.[14] The second clade comprises five "intermediate" species that may cause mild disease in humans. [14] The remaining seven
species are in the "saprophytes" clade which are known to consume decaying matter (saprotrophic nutrition).[14] Pathogenic Leptospira do not
multiply in the environment. Leptospira require high humidity for survival but can remain alive in environments such as stagnant water or
contaminated soil. The bacteria can be killed by temperatures of 50 °C (122 °F) and can be inactivated by 70% ethanol, 1% sodium
hypochloride, formaldehyde, detergents, and acids.[25]
Leptospira are also classified based on their serovar. The diverse sugar composition of the lipopolysaccharide on the surface of the spirochete is
responsible for the antigenic difference between serovars.[30] About 300 pathogenic serovars of Leptospira are recognized.[14] Antigenically related
serovars (belonging to the same serogroup) may belong to different species because of horizontal gene transfer of LPS biosynthetic genes
between different species.[14] Currently, the cross agglutination absorption test and DNA-DNA hybridisation are used to classify Leptospira species,
but are time consuming. Therefore, total genomic sequencing could potentially replace these two methods as the new gold standard of
classifying Leptospira species.[14]
Transmission[edit]
The bacteria can be found generally in various water-logged environments such as muddy riverbanks, ditches, gullies, and muddy livestock rearing
areas where there is a regular passage of wild or farm mammals. [31] The L. interrogans species can survive in low nutrient environments such as
moist soil and fresh water for prolonged periods.[27] However, L. borgpetersenii is devoid of critical genes necessary for survival in the environment.
[27]
Pathogenic Leptospira have been found in the form of aquatic biofilms, which may aid survival in the environment. [32]
The incidence of leptospirosis correlates directly with the amount of rainfall, making the disease seasonal in temperate climates and year-round in
tropical climates.[31] The risk of contracting leptospirosis depends upon the risk of disease carriage in the community and the frequency of exposure.
[19]
In rural areas, farming and animal husbandry are the major risk factors for contracting leptospirosis. [27] Poor housing and inadequate sanitation
also increase the risk of infection.[19] In tropical and semi-tropical areas, like South and South-east Asia, the disease is often
become widespread after heavy rains, sometimes after flooding. Periods of heavy rain followed by days of little or no rain seemed to be the setting
for leptospirosis epidemics in these parts of the world. [33]
The bacteria is carried by various animals. Although Leptospira have been detected in reptiles and birds, only mammals are able to transmit the
bacteria to humans and other animals.[34] Rats, mice, and moles are important primary hosts, but a wide range of other mammals including dogs,
deer, rabbits, hedgehogs, cows, sheep, swine, raccoons, opossums, skunks, and certain marine mammals carry and transmit the disease as
secondary hosts. In Africa, a number of wildlife hosts have been identified as carriers, including the banded mongoose, Egyptian fox, Rusa deer,
and shrews.[35] There are various machanisms where the animals can infect each other. Dogs may lick the urine of an infected animal off the grass
or soil, or drink from an infected puddle. House-bound domestic dogs have contracted leptospirosis, apparently from licking the urine of infected
mice in the house.[19] Leptospirosis can also be transmitted via the semen of infected animals. [31] The duration of bacteria being consistently present
in animal urine are long. In some animals such as cows, the bacterial shedding can persist for one year. [25]
Leptospirosis is transmitted by the urine of an infected animal and is contagious as long as the urine is still moist. [34] Humans become infected
through contact with water, food, or soil that contains urine from these infected animals. This may happen by swallowing contaminated food or
water or through skin contact.[36] The presence of wounds or fissures on the legs are a risk factor for acquiring the infection. [27] Occupations at risk of
contracting leptospirosis include veterinarians, slaughterhouse workers, countryside rangers, farmers, sailors on rivers, sewer maintenance
workers, waste disposal facility workers, and people who work on derelict buildings. [37] Slaughterhouse workers can contract the disease through
contact with infected blood or body fluids.[9] The disease was once mostly work-related but is now often also related to adventure tourism and
recreational activities.[6] Leptospirosis is common among water-sports enthusiasts in specific areas, as prolonged immersion in water promotes the
entry of the bacterium. Surfers and whitewater paddlers [36] such as rowers, kayakers and canoeists[9] However, Leptospira is unlikely to penetrate
intact skin.[21] The disease is not known to spread between humans, and bacterial dissemination in recovery period is extremely rare in humans.
[21]
Once humans are infected, bacterial shedding from the kidneys usually persists for up to 60 days. [25]
Rarely, leptospirosis can be transmitted through organ transplant. [38] Infection through the placenta during pregnancy is also possible.[39][40]
[41]
Leptospirosis can cause miscarriage and infection in infants.[42]

Pathogenesis[edit]
When animals ingest the bacteria, the bacteria circulate in the blood stream, then lodge themselves into the kidneys through
the glomerulular or peritubular capillaries. The bacteria then pass into the lumens of the renal tubules and colonise the brush border and proximal
convoluted tubule. This causes the continuous shedding of bacteria in the urine without the animal experiencing significant ill effects. This
relationship between the animal and the bacteria is known as commensal relationship and the animal is known as a reservoir host.[19]
Humans are the accidental host for leptospirosis.[27] The bacteria enters the human body through breaches in the skin or through the mucous
membrane, then into the bloodstream. The bacteria later attach to the endothelial cells of the blood vessels and extracellular matrix (complex
network of proteins and carbohydrates that present between the cells). The flagella of the bacteria help it move between cell
layers. Leptospira binds to a variety of cells such as fibroblasts, macrophages, endothelial cells, and kidney epithelial cells.[14] Additionally, surface
leptospiral immunoglobulin-like (Lig) proteins such as LigB, whose gene is found in all pathogenic Leptospira species, help Leptospira bind to
several proteins such as complement proteins, thrombin, fibrinogen, and plasminogen.[14]
Through innate immune system, endothelial cells of the capillaries in the human body are activated by the presence of these bacteria. The
endothelial cells produce cytokines and antimicrobial peptides against the bacteria. These products regulate the coagulation cascade and
movements of white blood cells.[14] Macrophages presented in humans are able to engulf Leptospira. However, Leptospira are able to reside and
proliferate in the cytoplasmic matrix after being ingested by human macrophages, which later results in the death of the macrophages.[27] Those
with severe leptospirosis can experience a high level of cytokines such as Interleukin 6, Tumor necrosis factor alpha (TNF alpha), and Interleukin
10. The high level of cytokines causes sepsis-like symptoms which is life-threatening instead of helping to fight against the infection. Those who
have high risk of sepsis during a leptospirosis infection are found to have the HLA-DQ6 genotype, possibly due to superantigen activation, which
damages bodily organs.[19]
Humoral immunity is the main immune response against the Leptospira cells. Agglutinating antibodies such as Immunoglobulin
M and Immunoglobulin G antibodies are produced against the bacteria. Such antibodies are mainly directed against the LPS.[27] Leptospira’s LPS
only activates toll-like receptor 2 (TLR2) in monocytes in humans. The Lipid A molecule of the bacteria is not recognized by
human TLR4 receptors. Therefore, the lack of Leptospira recognition by TLR4 receptors probably contributes to leptospirosis disease process in
humans.[27]
Although there are various mechanisms in the human body to fight against the bacteria, the Leptospira is well adapted to such inflammatory
condition created by the human body.[14] In the bloodstream, Leptospira can activate host plasminogen to become plasmin that breaks down
extracellular matrix, degrades fibrin clots and complemental proteins (C3b and C5) to avoid opsonisation. The bacteria can also recruit
complement regulators such as Factor H, C4b-binding protein, factor H-like binding protein, and vitronectin to prevent the activation of membrane
attack complex on its surface. Leptospira also secretes proteases to degrade complement proteins such as C3. Leptospira can bind to thrombin
that decreases the fibrin formation. Reduced fibrin formation increases the risk of bleeding. [14] Specifically, the L. interrogans serovar Pomona has
the SphA gene, which codes for Sphingomyelinase C that break down red blood cells. L. interrogans serovar Lai has the SphH gene, which codes
for pore-forming protein and the sph2 gene where both of them damage the membranes of red blood cells.[27]
Leptospira spreads rapidly to all organs through the bloodstream. The bacteria are subsequently cleared from the human body except in the
kidneys where they persist.[14] Leptospira mainly affects the liver. Congested liver sinusoids and perisinusoidal spaces have been
reported. Leptospira tend to invade spaces between hepatocytes. Hepatocyte apoptosis has also been reported. The damaged hepatocytes and
hepatocyte intercellular junctions cause leakage of bile into blood, resulting in elevated levels of bilirubin in those with jaundice. Meanwhile, in the
lungs, petechiae or frank bleeding can be found at alveolar septum and spaces between alveoli.[19] Leptospira can cause mild to severe kidney
failure. This is possibly due to reduced expression of Sodium–hydrogen antiporter 3 at the proximal renal tubule, causing reduced water absorption
and increased urinary excretion. In humans, TLR2 detection of Leptospira causes inflammation of the kidney in the first two weeks of infection
which results in interstitial nephritis. The kidney failure can recover completely or ended up as atrophy and fibrosis.[19] Rarely, inflammation of the
heart muscles, coronary arteries, and aorta are found.[23]

Diagnosis[edit]

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

For those who are infected, a complete blood count may show high white cell count and low platelet count. When low hemoglobin count is present
together with low white cell count and thromobocytopenia, bone marrow suppression should be considered.[19] Erythrocyte sedimentation
rate and C-reactive protein may also be elevated.[21]
The kidneys are commonly involved in leptospirosis. Blood urea and creatinine levels will be elevated although the urine output is normal or high.
Leptospirosis causes increased potassium excretion in the urine, which leads to low potassium level in the blood[19] and low sodium level.[21] Thus,
those infected who have poor oral intake and high urine output will often have severe dehydration which increases the risk of death. [19] Urine
analysis may reveal the presence of protein, presence of white blood cells, and microscopic haematuria.[21] The bacteria then move into kidneys
after 10 days. Therefore, a urine culture will remain positive for leptospirosis from 10 days until 30 days of infection. [21]
For those with liver involvement, mild elevations of transaminases and direct bilirubin can be observed in liver function tests. The Leptospira
Icterohaemorrhagiae serogroup is most commonly associated with jaundice and elevated bilirubin levels. In those with glucose-6-phosphate
dehydrogenase deficiency, leptospirosis can contribute to acute hemolytic anaemia and conjugated hyperbilirubinemia.
[19]
Abnormal serum amylase and lipase levels (associated with pancreatitis) can be seen in those who are admitted into a hospital due to
leptospirosis. Impaired kidney function with creatinine clearance less than 50 ml/min is associated with elevated pancreatic enzymes.[19]
In those who have lung involvement, a chest X-ray may demonstrate diffuse alveolar opacities. [19] Both lungs are usually involved, with infection
more commonly at the bases and periphery of the lungs, which can be present as early as 24 hours of the infection. Other patterns such
as interstitial lung disease, pleural effusion, and ground-glass opacity of the lungs are uncommon.[43]
For those with severe headache that shows signs of meningitis, a lumbar puncture can be attempted. If infected, cerebrospinal fluid (CSF)
examination shows lymphocytic predominance with a cell count of 500/mm3, protein between 50 and 100 mg/ml, and normal glucose levels. These
findings are consistent with aseptic meningitis.[19]
Rapid detection of Leptospira can be done by detecting the IgM antibodies using ELISA. Typically, isolates of L. biflexa antigen are used to detect
the IgM antibodies. This test can quickly determine the diagnosis and help in early treatment of leptospirosis. However, the test specificity depends
upon the type of antigen used, the presence of antibodies from previous infections, and the presence of other diseases such as Epstein-Barr
virus infection, viral hepatitis, and cytomegalovirus infection can cause false positive results.[19] Other rapid screening test have been developed
such as dipsticks, latex and slide agglutination tests.[21]
The Microscopic Agglutination Test (MAT) is the reference test for the diagnosis of leptospirosis. [19] MAT is a test where human or animal serum is
mixed with various types of Leptospira antigens serovars. The mixture is then examined under a microscope to look for agglutination. The MAT is
then read by dark field microscopy. The highest dilution where 50% agglutination occurs is the end result. [19] MAT titres of 1:100 to 1:800 are
diagnostic of leptospirosis.[21] A fourfold or greater rise in titre of two sera taken at symptoms onset and at 3 to 10 days of disease onset confirms
the diagnosis. During the acute phase of the disease, MAT is not specific in detecting a serotype of Leptospira because of cross-reactivity between
the serovars.[19] In the convalescent phase, MAT is more specific in detecting the serovar types.[19] MAT requires a panel of live antigens and
requires laborious work.[23]
Leptospiral DNA can be amplified by using polymerase chain reaction (PCR) from serum, urine, aqueous humour, CSF, and autopsy specimens.
[19]
PCR can detect the presence of leptospiral DNA in blood even after the initiation of antibiotics. [21] It can also detect the presence of the bacteria
without the appearance of antibodies during the first few days of the infection. [23] During the first eight days of infection, the bacteria can be detected
by quantitative PCR and can reach as high is 106 bacteria per ml of blood.[19] The inability of human TLR4 to recognise the Leptospires allows the
bacterial titres to be significantly higher when compared to Enterobacteriaceae infections.[19] Although PCR can detect more cases when compared
to culture, it cannot detect the specific serotype of Leptospira, thus affecting its value in epidemiological studies.[19] MAT subsequently replaces
PCR in detecting Leptospira infection.[19]
Molecular typing such as pulsed-field gel electrophoresis, multilocus sequence typing, multiple loci VNTR analysis can identify Leptospira to
species level by analyzing 16S ribosomal RNA gene of isolates.[23]
Leptospira is a slow-growing bacteria. Blood samples containing Leptospira can be cultured in both liquid and solid media with nutrients such
as long-chain fatty acids, vitamin B1 and B12, and ammonium salts.[27] The most common medium used is Ellinghausen-McCullough-Johnson-
Harris medium (EMJH), which contains oleic acid, bovine serum albumin, and polysorbate,[27] incubated at 28 to 30 °C.[44] Other samples that can be
cultured are: CSF and peritoneal washings during the first week of infection, and urine samples from the second week of infection. However, since
survival of Leptospira is limited in urine, a phosphate buffered saline is used to enhance the bacteria growth in urine culture. Since contamination is
prevalent in urine cultures, antibiotics such as fluorouracil are used to inhibit the growth of other bacteria in culture. The cultures are examined
weekly under a dark field microscope until 13 weeks of incubation. [19]

Prevention[edit]

A notice board by a lakeside in Sarawak, Malaysia that warns against swimming in the lake as the pool has been tested positive for pathogenic Leptospira.

The incidence of leptospirosis cases can be reduced by improving housing, infrastructure, and sanitation standards. Rodent abatement efforts and
flood mitigation projects can also help to prevent leptospirosis. [19] Proper use of Personal protective equipment (PPE) by people who have a high
risk of occupational exposure can prevent leptospirosis infections in most cases. [19] Effective rat control and avoidance of urine contaminated water
sources are essential preventive measures.[6]
Human vaccines are available only in a few countries, such as Cuba and China.[6] Both human and animal vaccines only cover a few strains of the
bacteria.[45] Side effects such as nausea, injection site redness and swelling have been reported after the vaccine was injected. Since the immunity
induced by one serovar of Leptospirosis is only protective against that specific serovar of leptospirosis, trivalent vaccines have been developed.
[19]
However, leptospiral vaccines do not confer long lasting immunity to humans or animals. [14] Dog vaccines are effective for at least one year. [45]
Doxycycline has been provided once a week as a prophylaxis to minimize infections during outbreaks in endemic regions. [46] Doxycycline was
found to be effective in reducing the number of leptospirosis cases in military personnel undergoing exercises in the jungles. In another study,
doxycycline administered after exposure to antibiotics was found reduce the number of people with symptomatic disease after a heavy rainfall
in endemic areas.[19] However, there is no strong evidence that chemoprophylaxis is effective in containing outbreaks of leptospirosis, [47] and use of
antibiotics increases antibiotic resistance. Pre-exposure prophylaxis may be beneficial for individuals traveling to high-risk areas for a short stay. [48]

Treatment[edit]
Most leptospiral cases resolve spontaneously. Early initiation of antibiotics may prevent the progression to severe disease. Therefore, in resource
limited settings, antibiotics can be started once leptospirosis is suspected in history taking and examination. [19]
For mild leptospirosis, antibiotic recommendations such as doxycycline, azithromycin, ampillicin and amoxicillin were solely based on in
vitro testing.[21] In 2001, the World Health Organization published a report which recommended oral doxycycline (2 mg/kg up to 100 mg 12 hourly)
for 5 to 7 days for those with mild leptospirosis. Tetracycline, ampicillin, and amoxicillin can also be used in such cases.[49] However, in areas
where rickettsia and leptospirosis are both endemic, either azithromycin or doxycycline are the drugs of choice. [21]
Based on a 1988 study, intravenous (IV) benzylpenicillin (also known as penicillin G) is recommended for the treatment of severe leptospirosis.
[21]
Intravenous benzylpenicillin (30 mg/kg up to 1.2g 6 hourly) is used for 5 to 7 days. Amoxicillin, ampicillin, and erythromycin may also be used for
severe cases.[49] Ceftriaxone (1g IV every 24 hours for 7 days) and penicillin G (1.5 million units IV every six hours for seven days) have been
shown to have similar efficacy in treating severe leptospirosis. [19][21][50] In another study on severe leptospirosis conducted in 2004,
both cefotaxime (1g IV every six hours for seven days) and doxycycline (200 mg initially followed by 100 mg IV every 12 hours for seven days)
showed similar efficacy when compared to penicillin G (1.5 million units IV every six hours for seven days). [21][51] Therefore, there is no evidence on
risk of death reduction when comparing the usage of intravenous benzylpenicillin with ceftriaxone or cefotaxime. [21] Another study conducted in
2007 also showed no difference in efficacy between doxycycline (200 mg initially followed by 100 mg orally every 12 hours for seven days)
or azithromycin (2 g on day 1 followed by 1 g daily for two more days) for suspected leptospirosis. There was no difference in the resolution of
fever and azithromycin is better tolerated than doxycycline. [52][53][54]
Those who can be treated as outpatients should receive doxycycline or azithromycin. Doxycycline can shorten the duration of leptospirosis by two
days, improve symptoms, and prevent the shedding of organisms in urine. Azithromycin and amoxicillin are given to pregnant women and children.
[19]
Rarely, a Jarisch–Herxheimer reaction can develop in the first few hours after antibiotic administration. [21] However, according to a meta-
analysis done in 2012, the benefit of antibiotics in the treatment of leptospirosis was unclear although the use of antibiotics may reduce the
duration of illness by two to four days.[21][53] Another meta-analysis done in 2013 reached a similar conclusion. [21][54]
For those with severe leptospirosis, such as potassium wasting with high kidney output dysfunction, intravenous hydration and potassium
supplements should be given to prevent dehydration and hypokalemia. When acute kidney failure occurs, early initiation
of haemodialysis or peritoneal dialysis can help to improve survival. For those with respiratory failure, tracheal intubation with low tidal
volume improves survival rates.[19]
The use of corticosteroids has been proposed for the treatment of leptospirosis because Leptospira infection can induce the release of chemical
signals which promote inflammation of blood vessels in the lungs. However, there is insufficient evidence to determine whether the use of
corticosteroids is beneficial.[21][55]

Prognosis[edit]
The overall risk of death for leptospirosis is 5% to 10%. [27] For those with jaundice, the case fatality can increase to 5% to 15%. [25] For those infected
presented with confusion and neurological signs, they have a high risk of death. [19] Other factors that increase the risk of death include: reduced
urine output, age more than 36 years, and respiratory failure. [19] With proper care, most of those infected will recover completely. Those with acute
kidney failure may suffer persistent mild kidney impairment post recovery.[19] In those with severe lung involvement, the risk of death is 50 to 70%. [21]
Thirty percent of affected people may suffer chronic leptospirosis syndrome for up to two years which is characterized by weakness, muscle pain,
and headaches.[19] Eye problems can occur in 10% of those who recovered from leptospirosis. [25] These complications can range from mild anterior
uveitis to severe panuveitis (which involves all the three vascular layers of the eye) post recovery. In up to 80% of those infected, leptospira DNA
can be found in the aqueous humour of the eye.[19] The eye problems usually have good prognosis when being treated or they are self-limiting. [25]

Epidemiology[edit]
It is estimated that seven to ten million people are infected by leptospirosis annually. [12] One million cases of severe leptospirosis occur annually,
with 58,900 deaths.[13] Leptospirosis is found in both urban and rural areas in tropical, subtropical, and temperate regions. The risk of death is 5 to
10%.[27]
Annual rates of infection vary from 0.1 to 1 per 100,000 in temperate climates to 10 to 100 per 100,000 in tropical climates. [46][56] The disease is
persistently observed in South and Southeast Asia, Oceania, Caribbean, [27] Latin America and Africa.[25] Antarctica is the only place not affected by
leptospirosis.[25] In the United States, there were 100 to 150 leptospirosis cases annually. [57] In 1994, leptospirosis ceased to be a notifiable disease
in the United States except in 36 territories where leptospirosis are prevalent such as Hawaii, Texas, California, and Puerto Rico. [58] About 50% of
the cases occurred in Puerto Rico. In January 2013, leptosprirosis was reinstated as a nationally notifiable disease in the United States. [57]
The number of new cases of leptospirosis is difficult to estimate since many cases are not reported. There are many reasons for this, but the
biggest issue is differentiating the disease from other conditions with a similar presentation. [56] Laboratory testing is lacking in many areas.[56] The
global incidence of leptospirosis has been underestimated because most affected countries lack notification or notification is not mandatory. [19] In
the context of global epidemiology, the socioeconomic status of many of the world's population is closely tied to malnutrition; subsequent lack of
micronutrients may lead to increased risk of infection and death due to leptospirosis infection. [59] Micronutrients such as iron, calcium,
and magnesium represent important areas of future research.[59]
The number of cases increases during the rainy season in the tropics and during the late summer or early fall in Western countries. This happens
because leptospires survive best in fresh water, damp alkaline soil, vegetation, and mud with temperatures higher than 22 °C.[60] This also leads to
increased risk of exposure to populations during flood conditions, and leptospire concentrations to peak in isolated pools during drought. There is
no evidence of leptospirosis having any effect on sexual and age-related differences. [60] However, a major risk factor for development of the disease
is occupational exposure, a disproportionate number of working-aged males are affected. [60] There have been reported outbreaks where more than
40% of people are younger than 15.[60] Outbreaks that occurred after the 1940s in the United States have happened mostly in the late summer
seasons, which happens to be the driest part of the year. The people at the highest risk for leptospirosis are young people whose age ranges from
5–16 years old, and can also range to young adults. [61]

History[edit]
The disease was first described by Adolf Weil in 1886 when he reported an "acute infectious disease with enlargement of spleen, jaundice,
and nephritis."[16] Even before Weil's description, the disease was known as "rice field jaundice" in ancient Chinese text, "autumn fever", "seven-day
fever"[62], and "nanukayami fever"[63] in Japan; in Europe and Australia, the disease was associated with certain occupations with names such as
"cane-cutter's disease", "swine-herd's disease", and "Sclammfieber" (mud fever). [62] It has historically been known as "black jaundice", [64] or "dairy
farm fever" in New Zealand.[65] Leptospirosis was postulated as the cause of an epidemic among Native Americans along the coast of what is
now New England during 1616-19. The disease was most likely brought to the New World by Europeans.[66]
Leptospira was first observed in 1907 from a post mortem kidney tissue slice by Stimson using silver deposition staining technique. He called the
organism Spirocheta interrogans because the bacteria resembles a question mark.[62][67] In 1908, a Japanese research group led by Inada and Ito
first identified this bacterium as the causative agent of leptospirosis [68] and in 1916 noted its presence in rats.[69] Leptospirosis were frequently
contracted by coal mine workers in Japan. The organism was named Spirocheta icterohaemorrhagiae. The Japanese group also experimented
with the first leptospiral immunisation studies in guinea pigs. They demonstrated that by injecting the infected guinea pigs with sera
from convalescent humans or goats, passive immunity can be provided to the guinea pigs. In 1917, the Japanese group discovered rats as the
carriers of leptospirosis.[62] Unaware of the Japanese group's work, two German groups independently and almost simultaneously published their
first demonstration of transmitting leptospiral infection in guinea pigs in October 1915. They named the organism Spirochaeta
nodosa and Spirochaeta Icterogenes respectively.[62]
Leptospirosis was subsequently recognised as a disease of all mammalian species. In 1933, Dutch workers reported the isolation of Leptospira
canicola which specifically infects dogs. In 1940, the strain that specifically infects cattle was first reported in Russia. [62] In 1942, soldiers at Fort
Bragg, North Carolina were recorded to have an infectious disease which caused rash over their shinbones. This disease was later known to be
caused by leptospirosis.[19] By the 1950s, the number of serovars that infects various mammals had expanded significantly. In the 1980s,
leptospirosis was recognised as a veterinary disease of major economic importance. [62]
In 1982, there were about 200 serovars of Leptospira available for classification. The International Committee on Systematic Bacteriology's
subcommittee on Taxonomy of Leptospira proposed classifying these serovars into two big groups: L. interrogans containing pathogenic serovars
and L. biflexa containing saprohytic serovars.[62] In 1979, the leptospiral family of Leptospiraceae was proposed. In the same year, Leptospira
illini was reclassified as the new genus Leptonema. In 2005, Leptospira parva was classified as Turneriella.[62] With DNA-DNA
hybridisation technology, L. interrogans was divided into seven species. More Leptospira species have been discovered since then. [62] The WHO
established the Leptospirosis Burden Epidemiology Reference Group (LERG) to review the latest disease epidemiological data of leptospirosis,
formulate a disease transmission model, and identify gaps in knowledge and research. The first meeting was convened in 2009. In 2011, LERG
estimated that the global annual incidence of leptospirosis is 5 to 14 cases per 100,000 population. [19]