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Test Code MUMPR Mumps Virus, Molecular Detection, PCR, Buccal


Ordering Guidance


Polymerase chain reaction testing (this test) is recommended as the first-line test if a patient has symptoms of mumps (ie, fever, swollen salivary/parotid glands).

 

If serology has been performed and IgM-class antibodies against mumps are detected (MMPGM / Mumps Virus Antibody, IgM and IgG, Serum), this test should be ordered to confirm mumps infection.



Shipping Instructions


Specimens should be transported as soon as possible.



Specimen Required


Specimen Type: Buccal Swab

Supplies: Culturette (BBL Culture Swab) (T092)

Container/Tube: Sterile container with transport media

Specimen Volume: Entire collection

Collection Instructions:

1. Collect specimen by swabbing back and forth over mucosal surface around buccal cavity (the space near the upper rear molars between the cheek and the teeth) to maximize recovery of cells.

2. Swab must be placed into viral transport media (eg, M4-RT, M4, M5, Barthels FlexTrans Media or Jiangsu Transport Media)


Useful For

Rapid qualitative detection of mumps virus using buccal swab specimens

Reporting Name

Mumps Virus PCR, Buccal

Specimen Type

Swab

Specimen Minimum Volume

0.3 mL

Specimen Stability Information

Specimen Type Temperature Time Special Container
Swab Refrigerated (preferred) 7 days
  Frozen  7 days

Reject Due To

E-swab, calcium alginate-tipped swab, wood swab, dry swab, or transport swab containing gel or charcoal additive  Reject
Throat swab Reject

Reference Values

Negative

Supportive Data

The following validation data support the use of this assay for clinical testing.

 

Accuracy:

Accuracy studies were performed by testing negative and positive (near the limit of detection) urine and buccal swab samples. Both urine and buccal swabs yielded 100% positive agreement and 100% negative agreement with expected results.

 

Analytical Sensitivity/Limit of Detection:

The lower limit of detection of this assay is 1.25 genome copies/mcL for urine and buccal swabs.

 

Precision:

Inter-assay and intra-assay precisions were 100%.

 

Specificity:

No sequences were identified that would result in cross-reactivity with the assay by in silico analysis. No cross-reactivity was detected in experiments testing a panel of nucleic acid extracts from more than 50 bacterial, fungal, and viral organisms causing similar disease or commonly found in urine or buccal swabs.

 

Reportable Range:

This is a qualitative assay, and the results are reported as either negative or positive for the mumps virus target.

Day(s) Performed

Monday through Friday

Report Available

1 to 3 days

Specimen Retention Time

1 week

Performing Laboratory

Mayo Clinic Laboratories in Rochester

CPT Code Information

87798

LOINC Code Information

Test ID Test Order Name Order LOINC Value
MUMPR Mumps Virus PCR, Buccal 47532-7

 

Result ID Test Result Name Result LOINC Value
617823 Mumps Virus PCR, Buccal 47532-7