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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, Urine

Specimen Type

Urine

Specimen 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 days

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Test 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