Test Code VZIKM Zika Virus, IgM Antibody Capture ELISA, Serum
Ordering Guidance
For specimens collected less than 14 days post-symptom onset or possible Zika virus exposure, reverse transcription polymerase chain reaction testing for Zika virus using serum and urine is recommended to exclude a false-negative Zika virus IgM result. For more information see VZIKU / Zika Virus, PCR, Urine and VZIKS / Zika Virus, PCR, Serum.
Additional Testing Requirements
This is a screening test for Zika virus. As required by your local health department, confirmatory testing of a presumptive positive result may be necessary.
Due to similar clinical presentation and cross reactivity, testing for IgM-class antibodies to dengue virus is recommended to occur concurrently with Zika virus IgM testing. Order DENVP / Dengue Virus Antibody/Antigen Panel, Serum.
Specimen Required
Collection Container/Tube:
Preferred: Serum gel
Acceptable: Red top
Submission Container/Tube: Plastic vial
Specimen Volume: 1 mL
Collection Instructions:
1. Allow blood to clot at room temperature (20-25° C) for 30 to 60 minutes, then centrifuge and aliquot serum into plastic vial.
2. Send serum specimen frozen.
Useful For
Screening for the presence of IgM-class antibodies to Zika virus
This test is not intended for medical-legal use.
This test is not recommended for asymptomatic couples attempting conception.
Special Instructions
Method Name
IgM Antibody Capture Enzyme-Linked Immunosorbent Assay (MAC-ELISA)
Reporting Name
Zika Virus MAC-ELISA, IgM, SSpecimen Type
SerumSpecimen Minimum Volume
0.8 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Serum | Frozen | 30 days |
Reference Values
Negative
Interpretation
See Assessment for Zika Virus Infection for a review of the recommended testing and interpretation of results. For the most recent Centers for Disease Control and Prevention guidelines for Zika virus testing visit  www.cdc.gov/zika/index.html
Presumptive Zika Positive:
IgM-class antibodies to Zika virus (ZIKV) detected. This is a preliminary result and does not confirm evidence of ZIKV infection. Confirmatory testing may be required as determined by your local health department. False-positive results may occur in patients with other current or prior flavivirus infections (eg, dengue virus). For patients with less than 7 days of symptoms or last possible exposure to ZIKV, reverse transcription polymerase chain reaction (RT-PCR) for ZIKV on serum and urine is recommended. A positive ZIKV RT-PCR result on either specimen is confirmatory for ZIKV infection.
Other Flavivirus Positive:
Antibodies to a flavivirus, not ZIKV, were detected. Consider targeted testing for IgM-class antibodies to dengue and/or West Nile viruses as appropriate, taking into consideration patient exposure and presentation.
Negative:
No evidence of IgM-class antibodies to ZIKV. For specimens collected less than 7 days post symptom onset or possible ZIKV exposure, RT-PCR for ZIKV on serum and urine to exclude a false-negative ZIKV IgM result is recommended. For symptomatic patients with travel to dengue endemic areas, testing for IgM antibodies to dengue virus is also recommended.
Clinical Reference
1. Oduyebo T, Polen KD, Walke HT, et al. Update: Interim guidance for health care providers caring for pregnant women with possible Zika virus exposure-United States (Including U.S. Territories), July 2017. MMWR Morb Mortal Wkly Rep. 2017;66(29):781-793
2. Waggoner JJ, Pinsky BA. Zika virus: Diagnostics for an emerging pandemic threat. J Clin Microbiol. 2016;54(4):860-867
3. Theel ES, Hata DJ. Diagnostic testing for Zika virus: a post outbreak update. J Clin Microbiol. 2018;56(4):e01972-17. doi:10.1128/JCM.01972-17
Day(s) Performed
Bimonthly on the first and third Wednesday; fifth Wednesday when applicable
Report Available
Same day/1 to 14 daysPerforming Laboratory
Mayo Clinic Laboratories in RochesterTest Classification
This test has been cleared, approved, or is exempt by the US Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.CPT Code Information
86794
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
VZIKM | Zika Virus MAC-ELISA, IgM, S | 80824-6 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
VZIKM | Zika Virus MAC-ELISA, IgM, S | 80824-6 |
Forms
If not ordering electronically, complete, print, and send an Infectious Disease Serology Test Request (T916) with the specimen.