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Molecular Detection

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Requisition Forms

Reference Details

Description:

Molecular detection of Leptospira species in clinical specimens.

Test Category:
Molecular Detection
Pathogen:
Leptospira spp.
Laboratory:
Illnesses and Diseases:
  • Leptospirosis
Specimen:

Whole blood, urine, tissue or cerebrospinal fluid (CSF). Minimum required volumes are as follows:

• Whole Blood – 0.5 mL
• Urine (fresh) – 5 mL
• Tissue – 1-5 mg
• CSF – 0.5 mL

Collection Method:

Collect blood in EDTA tubes. Avoid heparin. Do not centrifuge. Aseptically collect samples into sterile, leak-proof container made of freeze-thaw and shatter-resistant plastic, without additives.

Specimen Processing, Storage and Shipping:

Store specimens refrigerated up to 5 days and ship with freezer packs. If > 5 days, freeze at -20 °C and ship on dry ice.

Transportation of Dangerous Goods:

Shipping of specimens shall be done by a TDG certified individual in accordance with TDG regulations. For additional information regarding classification of specimens for the purposes of shipping, consult either Part 2 Appendix 3 of the TDG Regulations or section 3.6.2 of the IATA Dangerous Goods Regulations as applicable.

 

Patient Criteria:

Symptoms of Leptospira spp. infection may include fever, headache, chills, severe malaise, skin rash, vomiting, diarrhea, myalgia, conjunctival suffusion, jaundice, kidney and/or liver failure, meningitis and chest pains. Contact with an infected animal (dogs, cattle, raccoons, rodents, etc.) or recent travel to locations known to be endemic for Leptospira spp.

Accompanying Documentation:

Completed Requisition for Molecular Testing for Selected Zoonotic Agents.

Comments:

Specimens may be subject to rejection if they are not the appropriate sample type, have insufficient volume or not accompanied by relevant patient information or clinical history. This test is performed for investigational purposes.

Methods and Interpretation of Results:

Testing is performed, in whole or in part, using a lab-developed test which has not been fully validated/verified.

Extracted DNA is screened by an in-house real-time PCR assay specific for Leptospira spp. Samples that screen positive are subject to confirmatory testing. Initiation of antibiotic treatment prior to testing may result in decreased bacterial genome which will affect the outcome of PCR testing.

Turnaround Time:

21 calendar days.

Contact:
Phone #: (204) 789-6068
Fax: (204) 789-2082
References:
  1. Levett, P.N. Leptospirosis (2001) Clin. Micro. Rev. (14): 296-326.
  2. Stoddard R. A., Gee J. E., Wilkins P. P., McCaustland K., et al.2009. Detection of pathogenic Leptospira spp. through TaqMan polymerase chain reaction targeting the LipL32 gene. Diagn. Microbiol. Infect. Dis. 64:247–255.
  3. Mohd Ali, MR et. al., Development and validation of pan-Leptospira Taqman qPCR for the detection of Leptospira spp. in clinical specimens. Molec and Cell Probes 38 (2018) 1-6
Guidelines:
Related Information: