Molecular Detection of Yellow Fever Virus by Real-Time Reverse Transcriptase PCR (RT-PCR)<<Return to Laboratory
Molecular detection of Yellow Fever virus (YF) by real-time reverse transcriptase PCR.
- Yellow fever
Serum is the preferred specimen; however testing may also be performed on plasma or cerebral spinal fluid (CSF). Other bodily fluids and tissues may be considered for testing, please contact the Viral Zoonoses laboratory to verify suitability. Minimum volume of 600 µl.
Collect blood in serum separator tubes – submit in 2 ml O-ring tube.
Store samples frozen until shipped for testing. Ship samples on dry 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 YF virus infection and relevant travel history.
Completed Viral Zoonoses requisition including sender laboratory name, address and telephone number. Patient name and / or identifier (specimen reference number), date of birth, test(s) requested, collection date of specimen, date of on-set of symptoms, type of specimen, and clinical and travel history of patient.
This is not a routine test. Please contact the Viral Zoonoses Diagnostic Laboratory before sending specimens.
Yellow Fever virus real-time RT-PCR based on TaqMan chemistry. Two separate singleplex assays are performed targeting two distinct genomic regions; a result is classified as positive if both targets are detected and each Ct value falls within a pre-established cut-off value for each assay. If only a single target is detected, the test is repeated and/or other testing platforms may be enlisted to resolve the interpretation of the result.
Please contact the laboratory for the turnaround time.
- Lee, E., Lobigs M. (2008). E protein domain III determinants of yellow fever virus 17D vaccine strain enhance binding to glycosaminoglycans impede virus spread, and attenuate virulence. Journal of Virology, 82, 6024-6033.