Immunofluorescence Assay (IFA) - IgG

Immunofluorescence Assay (IFA) IgG to Coxiella burnetii.

• Q fever

Serum sample. Minimum volume required – 0.5 mL.

Submit in a sterile microcentrifuge tube.

Store samples refrigerated or frozen until shipped for testing. Ship frozen samples on dry ice, and refrigerated samples on wet ice

Shipping of specimens shall be done by a TDG certified individual in accordance with TDG regulations. For additional information regarding classification of specimens for the purposes of shipping, consult either Part 2 Appendix 3 of the TDG Regulations or section 3.6.2 of the IATA Dangerous Goods Regulations as applicable.

Suspected Q fever infection.

Completed Rickettsia and Related Zoonotic Diseases requisition including sender name, address and telephone number. Patient name or identifier (referring lab #), date of birth, suspected exposure, test(s) requested, clinical history. Type of specimen and date collected. If possible, include the antibiotics administered and travel history.

N/A

Testing is performed, in whole or in part, using an IVD testing kit which has not been fully validated/verified due to a lack of well-characterized panel.

Samples are screened for antibodies to C. burnetii phase I and phase II antigen using the Focus Diagnostics Q fever IFA IgG kit. 

15 calendar days.

Pathogen Safety Data Sheets: Infectious Substances – Coxiella burnetii

Q Fever