Test Code MEASU Measles Virus, Molecular Detection, PCR, Urine
Ordering Guidance
Polymerase chain reaction testing (this test) is recommended as the first-line test if a patient has symptoms of measles (ie, cough, fever, conjunctivitis, rash).
If serology has been performed and IgM-class antibodies against measles are detected (ROGM / Measles (Rubeola) Virus Antibody, IgM and IgG, Serum), this test should be ordered to confirm measles infection.
Shipping Instructions
Specimens must be shipped at refrigerated temperature. Specimens received frozen will be rejected.
Specimen Required
Supplies: Urine Tubes, 10 mL (T068)
Container/Tube: Plastic, 10-mL urine tube
Specimen Volume: 1 mL
Collection Instructions:
1. Collect a random urine specimen.
2. No preservative
Useful For
Identifying measles infection using random urine specimens
Method Name
Real-Time Polymerase Chain Reaction (PCR)
Reporting Name
Measles Virus PCR, UrineSpecimen Type
UrineSpecimen Minimum Volume
0.3 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Urine | Refrigerated | 7 days |
Reject Due To
Samples that have been heat inactivated Urine containing preservatives |
Reject |
Clinical Information
Measles virus is a single-stranded, negative-sense RNA paramyxovirus belonging to the genus Morbillivirus that causes acute respiratory illness. Symptoms of infection include fever, malaise, cough, coryza, and conjunctivitis. Following the onset of symptoms, individuals typically develop a pathognomonic enanthema (Koplik spots) followed by a maculopapular rash. Measles virus is transmitted via inhalation of aerosols or respiratory droplets and is highly contagious. Measles virus can also be transmitted by direct contact with infected secretions or contaminated fomites. Laboratory confirmation of measles cases can be through serologic detection of measles-specific IgM antibodies or molecular detection of measles virus RNA. The use of reverse-transcription polymerase chain reaction can provide increased sensitivity and specificity compared to serologic testing if specimens are collected early after rash onset. Collection of both respiratory and urine samples for analysis is recommended to increase the likelihood of detecting the virus.
Reference Values
Negative
Day(s) Performed
Monday through Friday
Report Available
1 to 3 daysPerforming Laboratory
Mayo Clinic Laboratories in RochesterTest Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.CPT Code Information
87798