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Test ID MGRP Mycoplasma genitalium, Molecular Detection, PCR

Useful For

Rapid, sensitive, and specific identification of Mycoplasma genitalium from genitourinary and reproductive sources

Method Name

Real-Time Polymerase Chain Reaction (PCR) Using LightCycler and Fluorescent Resonance Energy Transfer (FRET)
(PCR is utilized pursuant to a license agreement with Roche Molecular Systems, Inc.)

Reporting Name

Mycoplasma genitalium PCR

Specimen Type

Varies

The high sensitivity of amplification by PCR requires the specimen to be processed in an environment in which contamination of the specimen by Mycoplasma genitalium DNA is not likely.

 

Forms: If not ordering electronically, complete, print, and send a Microbiology Test Request Form (T244) with the specimen (http://www.mayomedicallaboratories.com/it-mmfiles/microbiology_test_request_form.pdf).

 

Specimen source is required.

 

Submit only 1 of the following specimens:

 

Specimen Type: Swab

Sources: Cervix, urethra, urogenital, vaginal

Container/Tube:                                                  

Preferred: Culture swab transport system (Dacron or rayon swab with aluminum or plastic shaft with either Stuart or Amies liquid medium)

Acceptable: Swab in transport media: M4, M5 (Supply T484), universal transport medium, or ESwab

Specimen Volume: One Swab

Collection Instructions:

1. Vaginal: Collect specimen by swabbing back and forth over mucosa surface to maximize recovery of cells.

2. Urethra or Cervical: Collect specimen by inserting swab 1 to 3 cm and rotating 360 degrees.

3. Place swab back into swab cylinder.

 

Specimen Type: Fluid

Sources: Amniotic, pelvic, prostatic secretion, reproductive drainage, semen

Container/Tube:         

Preferred: Sterile container

Acceptable: Container with 3 mL of transport media: M4, M5 (Supply T484), or universal transport media

Specimen Volume: 1-2 mL

 

Specimen Type: Urine, kidney/bladder stone, ureter

Container/Tube: Sterile container

Specimen Volume: 10 mL or entire specimen

 

Specimen Type: Tissue

Sources: Placenta, products of conception, genitourinary

Container/Tube: Sterile container

Specimen Volume: 5 mm

Collection Instructions: Submit only fresh tissue.

Specimen Minimum Volume

Pelvic Fluid, Amniotic Fluid, Prostatic Secretions, Semen, Reproductive Drainage or Fluid: 1 mL; Urine: 2 mL; Swab: 1 swab

Specimen Stability Information

Specimen Type Temperature Time
Varies Refrigerated (preferred) 7 days
  Frozen  7 days

Clinical Information

Mycoplasma genitalium causes acute and chronic nongonococcal urethritis, cervicitis, and pelvic inflammatory disease. Culture isolation is technically challenging; PCR is the diagnostic test of choice.

Reference Values

Not applicable

Cautions

Interfering substances may affect the accuracy of this assay; results should always be interpreted in conjunction with clinical and epidemiological findings.

 

This test does not detect other mycoplasmas or ureaplasmas.

Day(s) Performed

Monday through Friday

Report Available

3 days

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