Research Article

A Two-Step Lyssavirus Real-Time Polymerase Chain Reaction Using Degenerate Primers with Superior Sensitivity to the Fluorescent Antigen Test

Table 1

FAT and RTCIT-negative samples from various species used for the evaluation of the specificity of the lyssavirus qRT-PCR.

SpeciesMatrixProvider FAT/RTCITGeneric lyssavirus
qRT-PCR

Bats (Pipistrellus, Myotis, and Eptesicus  serotinus)1Brain tissueRabies NRC, WIV-ISP, Belgium 100NegativeNegative
Red Fox (Vulpes  vulpes)1Brain tissueRabies NRC, WIV-ISP, Belgium 10NegativeNegative
Dog (Canis  Lupus  familiaris)1Brain tissueRabies NRC, WIV-ISP, Belgium 10NegativeNegative
Cat (Felix  cati)1Brain tissueRabies NRC, WIV-ISP, Belgium 10NegativeNegative
Mouse (Mus  Musculus)2Brain tissueRabies NRC, WIV-ISP, Belgium 20NegativeNegative
Human (Homo  Sapiens)3Cerebrospinal fluidRabies NRC, WIV-ISP, Belgium 10NegativeNegative
Human (Homo  Sapiens)3SalivaRabies NRC, WIV-ISP, Belgium 5NegativeNegative
Human (Homo  Sapiens)3Skin tissueRabies NRC, WIV-ISP, Belgium 1NegativeNegative

Samples collected on the Belgian territory between 2007 and 2012 in the frame of the national surveillance system to guarantee the rabies-free status of Belgium.
2Specific-pathogen-free female Swiss outbred laboratory mice obtained from Harlan (Boxmeer, The Netherlands).
3Patients with encephalitis symptoms sent to the national reference centre for rabies virus, Belgium.