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Epic Code LAB809 Leptospira, IgM, Serum

Additional Codes

Mayo code: LEPDT

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Useful For

Aids in the diagnosis of leptospirosis

Specimen Type


Specimen Required


Preferred: Serum gel

Acceptable: Red top

Specimen Volume: 0.3 mL

Collection Instructions: Serum should be collected according to standard practices. Acute and convalescent specimens obtained to determine seroconversion should be collected 2 or more weeks apart.

Laboratory Test Directory Note:

COLLECTION NOTE: Volumes listed are in serum or plasma, draw approximately 2 1/2 times the requested volume in whole blood.

Specimen Minimum Volume

0.1 mL


If not ordering electronically, complete, print, and send a Microbiology Test Request (T244) with the specimen.


This is test is intended to be used as an aid for the diagnosis of acute or recent leptospirosis due to infection with Leptospira species.


This is a qualitative immunodot test for detection of IgM-class antibodies to Leptospira species.

A negative result by this assay does not exclude the possibility of leptospirosis and all results must be correlated with clinical presentation and exposure history.

Specimen Stability Information

Specimen Type Temperature Time Special Container
Serum Refrigerated (preferred) 30 days
  Frozen  30 days

Reject Due To

Gross hemolysis Reject
Gross lipemia Reject


The temporal IgM immune response can vary among patients. Therefore, a single negative result by this assay should not be used to exclude diagnosis, especially in patients with symptoms suggestive of leptospirosis who have an appropriate exposure history.


This test does not distinguish between acute or past infection. Clinical correlation is required. Patients may remain seropositive for months to possibly years following resolution of disease; therefore, this test cannot be used to establish cure or response to therapy.

Clinical Information

Leptospirosis is a zoonotic disease of worldwide prevalence, though the majority of infections occur in warm, tropical climates. Wild mammals, typically rodents, are the primary, natural reservoir for pathogenic strains of Leptospira, however, domestic animals (eg, dogs) also represent a major source of human infection. Leptospira are Gram-negative spirochetes with at least 20 different species in the genus. Of these, at least 9 species are considered pathogenic, including the most common agent of leptospirosis, Leptospira interrogans.


Transmission occurs through indirect human contact (eg, via mucous membranes or abraded skin) with water, food, or soil contaminated with animal urine containing the Leptospira spirochetes. Following infection, the incubation period can range from 3 to 30 days depending on the inoculum dose and immune status of the individual.


The clinical manifestations of leptospirosis can vary, ranging from a mild, flu-like illness (eg, headache, malaise, fever, arthralgia, fatigue) to fulminant disease, with severe liver and kidney involvement. The latter manifestation was previously referred to as Weil disease. Leptospira organisms may be found in the blood at the onset of disease and can persist for approximately 1 week. Subsequently, spirochetes may be found in the urine and can persist for 2 to 3 months; however, shedding may be intermittent and the numbers of organisms present may be low.


While Leptospira can be grown in culture, this is a fastidious organism and requires immediate transport to the laboratory. Additionally, detectable growth requires prolonged incubation (1-6 weeks), limiting the utility of culture for acute diagnosis. For this reason, serologic detection for antibodies to Leptospira remains the method of choice for rapid diagnosis. IgM-class antibodies to this spirochete are detectable by day 6 of illness and remain detectable for 2 to 3 months following symptom onset.

Method Name

Enzyme-Linked Immunoassay Dot (Immunodot)

Report Available

Same day/1 to 5 days

Reporting Name

Leptospira, IgM, S

Reference Values




IgM antibodies to Leptospira species detected suggesting recent infection. Antibody presence alone cannot be used to definitively diagnose acute infection, as antibodies from a prior exposure or infection may remain detectable for a prolonged period of time.



Result should be interpreted with caution. Additional testing of a second, convalescent specimen is recommended. If the specimen remains borderline reactive, a second serological method should be considered if leptospirosis infection is still suspected.



No IgM antibodies to Leptospira detected. Since antibodies may not be present or may be present at undetectable levels during early disease, repeat testing of a convalescent sample collected in 2 to 3 weeks is recommended.

Method Description

The GenBio IgM ImmunoDOT Leptosirosis test utilizes an enzyme-linked immunoassay (EIA) dot technique for the detection of IgM antibodies. Leptospira biflexa, serovar Patoc 1 strain antigens are dispensed as discrete dots onto a solid membrane. After adding the test specimen to a reaction cuvette, an assay strip is inserted, allowing patient antibodies reactive with the test antigens to bind to the strip's solid support member. Alkaline phosphatase conjugated goat antihuman IgM antibodies are allowed to react with bound patient antibodies. Finally, the strip is transferred to an enzyme substrate reagent, which reacts with bound alkaline phosphatase to produce an easily seen, distinct spot.(Package insert: ImmunoDOT Leptospira IgM. GenBio;06/2019)

Day(s) Performed

Monday, Wednesday, Friday

Clinical Reference

1. Centers for Disease Control and Prevention, National Center for Emerging and Zoonotic Infectious Diseases (NCEZID), Division of High-Consequence Pathogens and Pathology (DHCPP): Leptospriosis. Reviewed March 13, 2019. Accessed October 16, 2020. Available at

2. Costa F, Hagan JE, Calcagno J, et al: Global morbidity and mortality of Leptospirosis: A systemic review. PLoS Negl Trop Dis. 2015 Sept;9(9):e0003898 doi: 10.1371/journal.pntd.0003898

Test Classification

This test has been cleared, approved, or is exempt by the US Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.

CPT Code Information


LOINC Code Information

Test ID Test Order Name Order LOINC Value
LEPDT Leptospira, IgM, S 23201-7


Result ID Test Result Name Result LOINC Value
65183 Leptospira, IgM, S 23201-7