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. 2019 Dec 24;67(3):1189–1197. doi: 10.1111/tbed.13452

Table 4.

The results of virologic and serologic testing of in‐contact horse sera housed at the same stables of the first equine WNND case in Austria in 2016

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.

a

Commercial ELISA kits (IDVet) were used to measure the presence of IgG and IgM antibodies reactive to West Nile virus (WNV) antigen.

b

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).