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Department of Health Services

Public Health Regional Laboratory

Zika-only virus detection (CDC Trioplex), RT-PCR

The Trioplex Real-time RT-PCR Assay (Trioplex rRT-PCR) is intended for the qualitative detection of Zika virus RNA in urine, and amniotic fluid (each collected alongside a patient-matched serum specimen).  For use in individuals who meet the Centers for Disease Control and Prevention (CDC) clinical and epidemiological criteria for Zika virus testing. Zika viruses are primarily transmitted by Aedes aegypti and Aedes albopictus mosquitos.

Portal Ordering Code

TRIO-PCR-URINE/AMNIO

CPT Code(s)

87662, 87798x2

Fee Schedule

Storage and Transport Criteria
Specimen Storage Specimen Transport
Acceptable Specimens
Minimum Volume
Frozen Range
-70°C - 0°C
Refrigerated Range
0.1°C - 8°C
Room Temperature Range
8.1°C - 30°C
Stability at
4°C - 25°C
Urine or amniotic fluid 1 mL ≤ -20°C upon receipt Reject Reject Dry ice or cold packs (acceptable)
Includes

Serum order choice is automatically ordered

Methodology

RT-PCR

Assay Category

EUA (Emergency Use Authorization)

Reference Range

See laboratory report

Alternative Names
  • Trioplex Real-time RT-PCR Assay
  • ZIKA virus
Preferred Specimen(s)
  • Urine
  • Amniotic fluid
Alternative Specimen(s)

N/A

Minimum Volume

1 mL 

Special Instructions

Collect serum in conjunction with urine or amniotic fluid.

Reject Criteria
  • Inadequately labeled specimens
  • Leaking specimens
  • QNS (quantities not sufficient)
  • Specimens not meeting the Storage & Transport criteria upon receipt at laboratory
Setup Schedule

Testing is performed on an as-needed basis.

Turn around time (TAT)

2 business days from arrival at the lab