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Test ID TOXB Toxoplasma gondii, Molecular Detection, PCR, Blood

Useful For

Supporting the diagnosis of active toxoplasmosis, particularly in immunocompromised individuals

Method Name

Polymerase Chain Reaction (PCR)/DNA Probe Hybridization

(PCR is utilized pursuant to a license agreement with Roche Molecular Systems, Inc.)

Reporting Name

Toxoplasma gondii PCR, B

Specimen Type

Whole Blood EDTA

Container/Tube: Lavender top (EDTA)

Specimen Volume: 1 mL

Specimen Minimum Volume

0.3 mL

Specimen Stability Information

Specimen Type Temperature Time
Whole Blood EDTA Refrigerated (preferred) 7 days
  Frozen  7 days

Clinical Information

Toxoplasma gondii is an intracellular protozoan parasite that chronically infects 10% or more of the adult population in the United States. Transmission may occur by ingestion of undercooked meat containing cysts, by direct contact with the feces of an infected cat excreting infectious oocysts, and vertically through the placenta. Accurate diagnosis is crucial because of the different therapeutic options.

 

Serology is the traditional method for diagnosing toxoplasmosis and ascertaining the previous exposure history of the host.(1) Active toxoplasmosis is suggested by the presence of IgM antibodies, but elevated anti-IgM titers are often absent in immunocompromised patients. In addition, elevated IgM can persist from an acute infection that may have occurred as long ago as 1 year. Serologic results may also be unreliable or challenging to interpret in immunocompromised patients and in suspected intrauterine infection.

 

Detection of Toxoplasma gondii DNA by PCR has proven to be a rapid and reliable alternative or supportive method for the diagnosis of toxoplasmosis. When performed on blood, it may detect circulating parasite DNA and thus confirm or support the results of serologic testing. PCR testing on peripheral blood has been used successfully to detect cases of ocular toxoplasmosis(2) as well as invasive disease in allogeneic stem cell recipients.(3,4)

Reference Values

Negative

Cautions

This assay is designed for use in patients with a clinical history and symptoms consistent with toxoplasmosis. This test should not be used to screen healthy patients.

 

Blood may not be a sensitive specimen for detecting organ specific disease (eg, ocular or cerebral toxoplasmosis). In this case, other specimens (eg, ocular fluid, CSF, fresh tissue) should be considered.

 

Results should be interpreted with consideration of clinical and laboratory findings. A negative result does not indicate absence of disease. Reliable results depend on adequate specimen collection and the absence of inhibiting substances.

Day(s) Performed

Monday through Saturday; Varies

Report Available

1 day/same day

Performing Laboratory

Mayo Medical Laboratories in Rochester

Test Classification

This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the U.S. Food and Drug Administration.

CPT Code Information

87798

NY State Approved

Yes