de Leeuw Olav S, Koch Guus, Hartog Leo, Ravenshorst Niek, Peeters Ben P H
Wageningen University and Research Centre, Animal Sciences Group, Division of Infectious Diseases, 8200 AB Lelystad, The Netherlands.
Central Institute for Animal Disease Control, PO Box 2004, 8203 AA Lelystad, The Netherlands.
J Gen Virol. 2005 Jun;86(Pt 6):1759-1769. doi: 10.1099/vir.0.80822-0.
Virulence of Newcastle disease virus (NDV) is mainly determined by the amino acid sequence surrounding the fusion (F) protein cleavage site, since host proteases that cleave the F protein of virulent strains are present in more tissues than those that cleave the F protein of non-virulent strains. Nevertheless, comparison of NDV strains that carry exactly the same F protein cleavage site shows that significant differences in virulence still exist. For instance, virulent field strain Herts/33 with the F cleavage site 112RRQRRF117 had an intracerebral pathogenicity index of 1.88 compared with 1.28 for strain NDFLtag, which has the same cleavage site. This implies that additional factors contribute to virulence. After generating an infectious clone of Herts/33 (FL-Herts), we were able to map the location of additional virulence factors by exchanging sequences between FL-Herts and NDFLtag. The results showed that, in addition to the F protein cleavage site, the haemagglutinin-neuraminidase (HN) protein also contributed to virulence. The effect of the HN protein on virulence was most prominent after intravenous inoculation. Interestingly, both the stem region and the globular head of the HN protein seem to be involved in determining virulence.
新城疫病毒(NDV)的毒力主要由融合(F)蛋白裂解位点周围的氨基酸序列决定,因为裂解强毒株F蛋白的宿主蛋白酶比裂解无毒株F蛋白的宿主蛋白酶存在于更多组织中。然而,对携带完全相同F蛋白裂解位点的NDV毒株进行比较发现,毒力仍存在显著差异。例如,具有F裂解位点112RRQRRF117的强毒野毒株Herts/33的脑内致病指数为1.88,而具有相同裂解位点的NDFLtag毒株的脑内致病指数为1.28。这意味着还有其他因素影响毒力。构建了Herts/33的感染性克隆(FL-Herts)后,我们通过交换FL-Herts和NDFLtag之间的序列来确定其他毒力因子的位置。结果表明,除了F蛋白裂解位点外,血凝素神经氨酸酶(HN)蛋白也对毒力有影响。HN蛋白对毒力的影响在静脉接种后最为明显。有趣的是,HN蛋白的茎区和球状头部似乎都参与了毒力的决定。