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Chikungunya virus

Clinical Specimen Submission Guidance

Submit all specimens to 150 Richmond Street, Suite 100, Providence, RI 02903. Open Monday to Friday 8:30 AM to 4:30 PM.   Learn how and where to drop off your lab samples at our Laboratory Central Services webpage.

Lab

STI & Arbovirus Laboratory 401-222-5591

Analyte Name

Chikungunya virus

Disease

Chikungunya Virus Infection (Chikungunya)

Test Description

Testing performed at RI State Health Laboratories (RISHL) -preauthorization required

PCR (whole blood): The BioFire Global Fever Special Pathogens Panel (GFSPP) is an FDA-cleared, qualitative, multiplexed, nucleic acid-based PCR assay. For additional information refer to: https://health.ri.gov/laboratory-testing/clinical-specimen-submission-guidance/global-fever-special-pathogens-panel

Note: When testing for mosquito-borne viruses (Chikungunya, Dengue, West Nile, Yellow Fever), the GFSPP may not reliably detect the presence of arbovirus RNA once patients are outside the acute phase of infection, namely the first 1 to 7 days after symptoms onset.

Testing performed at CDC -preauthorization required

Plaque Reduction Neutralization Test (PRNT) (serum) 

Special Instructions

PREAUTHORIZATION by RIDOH Center for Acute Infectious Disease Epidemiology (401) 222-2577 is required for both GFSPP and PRNT.

All specimens must be submitted to the CDC through State Health Departments and not submitted directly to CDC.

Specimen

All specimens should be acute (0-7 days post onset date).

Global Fever Panel (PCR: Collect 5 mL whole blood in EDTA tube and promptly store at 2° - 8°C. 

If specimen cannot be transported to RISHL within 24 hours, then the specimen should be frozen at or below -20°C.

Testing at CDC:

Serum: collect blood in red top tube or serum separator tube, spin, pour off serum and submit >= 2mL in a sterile plastic screw-capped tube. Store serum at 2° - 8°C.

Specimen Identification

CLIA regulations require specimens be labeled with at least two patient identifiers. Examples of identifiers are first and last name, date of birth, chart/medical record number. The specimen container must be labeled to match the test requisition or the electronic order.

Form Required

Rhode Island State Health Laboratories (RISHL) test requisition form https://health.ri.gov/forms/LabRequisitionForm.pdf

CDC 50.34 Form is required for PRNT testing

Test Request

Global Fever Special Pathogens Panel - prior approval from RIDOH Center for Infectious Disease Epidemiology required.

CDC Testing:

Write "Chikungunya PRNT" under Comments/Other Test Requests

Transport

Transport specimens as soon as possible. Must be received within 4 days of collection.

Contact the RISHL STI & Arbovirus Lab (401) 222-5591 prior to transport.

Refrigerated: Transport and deliver to the laboratory within 24 hours of collection at 2-8°C in a cooler able to maintain specimen temperature. A plug-in electric cooler is recommended, however, a cooler packed with excess frozen gel packs is acceptable as long as the transport temperature is maintained at 2-8°C. 

Frozen: If specimen previously frozen, it must be transported on frozen gel packs in insulated shipper.

Specimens must be transported and packaged in accordance with current federal shipping regulations.

Integrity

Non-Hemolyzed

Specimen Rejection Criteria

The following rejection criteria will be used to ensure accurate specimen information and specimen condition for testing:

  • Specimen received outside acceptable transport range
  • Demographics different / Unable to read identifiers on specimen
  • Two identifiers required on specimen
  • Expired / Incorrect collection kit
  • Insufficient quantity
  • No specimen received
  • Specimen leaked in transit
  • Specimen too old
Normal Value

Global Fever Panel (PCR): Not detected

 

Reporting Requirement

Providers must report patient information on Chikungunya Virus Infection immediately using the RIDOH reportable disease form.

Turnaround Time

GFSPP PCR = 1 day

PRNT = CDC 4 weeks

Note: The PRNT turnaround time listed includes the possibility that the test being ordered is part of a larger testing algorithm.