California Serogroup Serology and PCR

Testing Indications

California serogroup (CSG) viruses are mosquito-borne pathogens that may cause encephalitis in humans. CSG viruses circulate across Canada and the United States. Clinical cases as well as seroprevalence rates of 20-30% have been documented from coast to coast including northern regions of the country such as the Yukon and North West Territories. It is recommended that CSG viruses, and other arboviruses present in Ontario (e.g., West Nile, Powassan, Eastern equine encephalitis viruses) be part of the differential for neurological case investigations that occur during the active mosquito season. The National Microbiology Laboratory (NML) currently tests for the two most prevalent CSG viruses in Ontario and Canada, Jamestown Canyon and Snowshoe Hare viruses.1

Note: La Crosse virus, the most commonly documented CSG virus in the United States, is not present in Canada.

Specimen Collection and Handling

Specimen Requirements

Test Requested Required Requisition(s) Specimen Type Minimum Volume Collection Kit

California Group Serology

Paired serum specimens (acute AND convalescent) collected 2-3 weeks apart from patients with clinical illness2

Minimum volume of 1 mL for serological testing.

Red top or serum separator tubes

California Group Serology

Cerebrospinal fluid (CSF) paired with single serum from patients with clinical illness2

Minimum volume of 500 µL for serological testing.

Sterile tube/container and Red top or serum separator tubes

California Group Serology

Serum or CSF

Additional volume of 250 µL is required for molecular detection

Red top or serum separator tubes (serum) Or Sterile tube/container (CSF)

Submission and Collection Notes

1

Effective October 3, 2022, the Arbovirus (Non-Zika) Testing Intake Form  is a mandatory requirement for California encephalitis virus testing. PHO’s laboratory utilizes the information on the requisition and the mandatory intake form to assess testing criteria, assign appropriate tests, and provide mandatory information required by the National Microbiology Laboratory for relevant testing performed there.

2

Clinical information, including any risk factors such as mosquito exposure, and any recent travel, must be provided on the requisition before testing will be performed. Specimens not meeting NML’s acceptance criteria will be rejected for testing. Under special circumstances, testing will be considered on a case-by-case basis.

3

NML will not accept unpaired specimens. See Timing of specimen collection for details on paired specimen requirements.

4

Contact the PHO Customer service at 416-235-6556 or 1-877-604-4567 for further information.

Timing of Specimen Collection

The following paired specimens are accepted for CSG serology:

  1. Paired serum specimens (acute and convalescent) collected 2-3 weeks apart from patients with clinical illness
  2. CSF paired with single serum from patients with clinical illness.

Limitations

Persistent IgM and the high seroprevalence associated with CSG viruses in the Canadian population makes it difficult to differentiate recent from past infections from a single serum specimen, thus the need for paired sera and/or CSF.

PCR is not recommended for CSG viruses as it is not a sensitive test for CSG viruses, unless collected within 5 days of neurological onset during active mosquito season. NML will determine if molecular testing is feasible after serological testing is complete.

Preparation Prior to Transport

Specimens should be stored at 2-8°C or frozen following collection. Ship refrigerated specimens on ice packs and frozen specimens on dry ice.

Special Instructions

All specimens submitted for testing must be accompanied by a separate General Test Requisition for each specimen type collected. All fields on each requisition must be completed.

It is also MANDATORY to provide all information requested on the Arbovirus (Non-Zika) Information Intake Form. The Arbovirus (Non-Zika) Information Intake Form may be exempted if all mandatory information is available on the PHO’s General Test Requisition. Specimens submitted with missing mandatory information will not be tested until that information is provided.

Requisitions and Kit Ordering

Test Frequency and Turnaround Time (TAT)

The Turnaround Time (TAT) for IgM Enzyme Linked Immunosorbent Assay (ELISA) is 14 days from receipt at NML.

The TAT for the confirmatory Plaque Reduction Neutralization Test (PRNT) is 28 days from receipt at NML.

RT-PCR (if performed) is 14 days following the ELISA.

Reporting

Results are reported to the ordering physician or health care provider as indicated on the requisition.

Positive CSG results for encephalitis cases are reported to the Medical Officer of Health as per the Ontario Health Protection and Promotion Act.

Test Methods

Screening test: IgM ELISA only ; IgG ELISA not performed.

Confirmatory test : PRNT

Optional test: molecular detection by PCR


Algorithm

Submitted specimens will first be analyzed by the IgM ELISA to determine if the patient has developed antibodies. IgM-reactive specimens will undergo PRNT confirmation.

Note: IgG serology is not available/not performed at NML.

Specimens that are reactive will be further analyzed for the presence of neutralizing antibodies.

PCR testing will be considered on a case-by-case basis.

Mis à jour le 5 oct. 2022