Table 4.
Horse no. |
RT‐qPCR WNV |
IgMa | IgGa |
PRNT80b WNV |
PRNT80b TBEV |
PRNT80b USUV |
---|---|---|---|---|---|---|
1 | − | − | − | nt | nt | nt |
2 | − | − | − | nt | nt | nt |
3 | − | − | − | nt | nt | nt |
4 | − | − | +/− | − | nt | nt |
5 | − | − | − | nt | nt | nt |
6 | − | − | +/− | − | nt | nt |
7 | − | − | +/− | − | nt | nt |
8 | − | − | + | − | nt | nt |
9 | − | − | + | 1:80 | − | − |
10 | − | − | − | nt | nt | nt |
11 | − | − | − | nt | nt | nt |
12 | − | − | − | nt | nt | nt |
13 | − | − | + | 1:160 | − | − |
14 | − | − | + | − | nt | nt |
+, positive; −, negative; +/−, weak positive; nt, not tested.
Commercial ELISA kits (IDVet) were used to measure the presence of IgG and IgM antibodies reactive to West Nile virus (WNV) antigen.
Endpoint titres for 80% plaque reduction neutralization assay (PRNT80) were performed for antibody‐positive samples against WNV, tick‐borne encephalitis virus (TBEV) and Usutu virus (USUV).