Florida Bureau of Public Health laboratories
Arbovirus SN
Arbovirus PRNT is a lab developed test that measures the ability of antibodies to neutralize viruses.
Analyte(s)
Eastern equine encephalitis (EEE), St. Louis encephalitis (SLE), dengue (DEN), West Nile (WN), Zika (ZIK), and Oropouche (OROV)
Test Code
EEE: 1520, OROV:Â 1565, WNV & SLE:Â 1522, ZIK: 1536, or DEN: 1524
Testing Location
Testing Department
Virology
Pre-approval Required?
Yes.
Requires prior approval from regional epidemiology and notification to the testing lab. Contact the local county health department (CHD) to start the process for approval.
Required Forms
BPHL Test Requisition, DH1847
Include all required fields, who authorized the testing, onset date, collection date, travel history, and symptoms.
Turn Around time
7 – 21 business days after receipt at the laboratory
Minimum Volume
0.5 mL
Collection Media
Vacutainer (red stopper) or serum-separator tube (tiger/red – topped tube)
Specimen Sources
Serum: single sample or paired serum*
Specimen Labeling
Specimen must be labeled with at least two unique patient identifiers, e.g., name and DOB.
Information on the specimen must match the requisition and/or test order.Â
Special SPecimen Preparation
*Paired Sera Collection:
1. First specimen (acute) collected in red top tube 1-3 days after onset of illness. Separate serum and store refrigerated at 2 8° C until second specimen is collected.
2. Second specimen (convalescent) collected in red top tube 10-14 days after first specimen.
3. Ship sera together overnight at 2 – 8° C
Storage Conditions
Store specimens at 2 – 8° C or frozen at -20° C or lower until time of shipment.
Packaging and Shipping
Specimens should be shipped on frozen ice packs at 2 – 8° C or frozen on dry ice at -20° C or lower. It the specimens were stored frozen, then they should be shipped frozen to avoid a freeze thaw cycle.
Separate specimens into different bags to help prevent cross contamination.
Include paperwork with specimens but separate them physically by placing the paperwork in the outer pocket of the biohazard bag.
unsatisfactory specimen
1) Requisition form was not fully completed with all required fields
2) No patient identification on specimen tube
3) Patient identifiers on the specimen do not match the requisition or test order
4) Specimen damaged or leaked in transit
5) Specimen was received outside the required temperature range
Interferences and Limitations
None
Reference Range
Negative: Not detected
Result Indicator
Positive: Titer and interpretation
Negative: Not detected
Reference lab
CDC if needed
Reflex testing
None