Detection of Newcastle disease virus (NDV) and avian pathotyping of NDV iso
lates are extremely important because the appearance of virulent virus has
significant economic consequences in terms of vaccination, eradication, and
the ability to export poultry products. By using nucleotide and amino acid
(aa) homology analysis, we could demonstrate that a NDV broiler isolate is
a velogenic virus. This analysis was done after mean death time and intrac
erebral pathogenicity index tests gave inconsistent results. By establishin
g a nucleotide sequence dendrogram, we found that the disputed Ber-Tuvia wa
s clearly in the same group as the known Herev-Laet, a velogenic isolate. T
he difference between Ber-Tuvia 32 and the Herev-Laet velogenic isolate was
6% as opposed to >16% of the meso- and lentogenic isolates. The Ber-Tuvia
isolate contains the Arg/Arg and Lys/Arg aa at positions 112, 113 and 115,
116, respectively in the fusion protein cleavage aa sequence, which is typi
cal for virulent NDV isolates.