Test ID MPRP Mycoplasma pneumoniae, Molecular Detection, PCR
Useful For
Diagnosis of infections due to Mycoplasma pneumoniae
Special Instructions
Method Name
Rapid Polymerase Chain Reaction (PCR) Using Light Cycler and Fluorescent Resonance Energy Transfer (FRET)
(PCR is utilized pursuant to a license agreement with Roche Molecular Systems, Inc.)
Reporting Name
Mycoplasma pneumoniae PCRSpecimen Type
VariesThe high sensitivity of amplification by PCR requires the specimen to be processed in an environment in which contamination of the specimen by Mycoplasma pneumoniae DNA is unlikely.
Forms: If not ordering electronically, complete, print, and send 1 of the following forms with the specimen:
Microbiology Test Request Form (T244) (http://www.mayomedicallaboratories.com/it-mmfiles/microbiology_test_request_form.pdf)
Neurology Test Request Form (T732) (http://www.mayomedicallaboratories.com/it-mmfiles/neurology-request-form.pdf)
Specimen source is required.
Submit only 1 of the following specimens:
Specimen Type: Respiratory
Sources: Bronchial washing, bronchoalveolar lavage, tracheal secretions, sputum
Container/Tube:
Preferred: Sterile container
Acceptable: Specimen in M4, M5, or UTM
Specimen Volume: 1 mL
Specimen Type: Swab
Sources: Throat, nasal, or nasopharyngeal
Container/Tube:
Preferred: Culture swab transport system (Dacron or rayon swab with aluminum or plastic shaft with either Stuart or Amies liquid medium)
Acceptable: Culture transport swab (Stuart's media) or place swab in M4, M5, UTM, or ESwab
Specimen Volume: Swab
Collection Instructions:
1. Collect specimen by swabbing back and forth over mucosa surface to maximize recovery of cells.
2. Place swab back into swab cylinder.
Specimen Type: Fluid
Sources: Pleural, pericardial, cerebrospinal
Container/Tube: Sterile vial
Specimen Volume: 0.5 mL
Specimen Minimum Volume
Respiratory: 0.5 mL; Fluid: 0.5 mL; Swab: 1 swab
Specimen Stability Information
Specimen Type | Temperature | Time |
---|---|---|
Varies | Refrigerated (preferred) | 7 days |
Frozen | 7 days |
Clinical Information
Mycoplasma pneumoniae is a small bacterium transmitted via organism-containing droplets. It is a cause of upper respiratory infection, pharyngitis, and tracheobronchitis, particularly in children, and has been associated with approximately 20% of cases of community acquired pneumonia.(1) Central nervous system and cardiac manifestations are probably the most frequent extrapulmonary complications of infections due to Mycoplasma pneumoniae. The disease is usually self-limited although severe disease has been reported in immunocompromised patients.(2)
Identification of Mycoplasma pneumoniae by culture-based methods is time consuming and insensitive. Serology based assays for Mycoplasma pneumoniae have several drawbacks. The development of IgM antibodies takes approximately 1 week and the IgM response in adults may be variable or it may be decreased in immunosuppressed individuals.(3,4) Confirmation of the disease may be dependent on the observation of a 4-fold rise in IgG antibody titers between acute and convalescent specimens, several weeks following the initial onset of illness, providing clinical utility only for retrospective testing.(4) Real-time PCR offers a rapid and sensitive option for detection of Mycoplasma pneumoniae DNA from clinical specimens.
Reference Values
Not applicable
Cautions
This assay should only be used for testing of respiratory tract specimens (throat swabs, nasopharyngeal swabs, tracheal secretions, sputum, and bronchoalveolar lavage fluid) and pleural/chest fluid, pericardial fluid, and cerebrospinal fluid.
Day(s) Performed
Monday through Sunday
Report Available
3 daysPerforming Laboratory

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
87581