US Geological Survey, Alaska Science Center, 4210 University Drive, Anchorage, AK, 99508, USA,
Arch Virol. 2013 Dec;158(12):2495-503. doi: 10.1007/s00705-013-1761-0. Epub 2013 Jun 27.
Avian paramyxovirus serotype 1 (APMV-1), or Newcastle disease virus, is the causative agent of Newcastle disease, one of the most economically important diseases for poultry production worldwide and a cause of periodic epizootics in wild birds in North America. In this study, we examined the genetic diversity of APMV-1 isolated from migratory birds sampled in Alaska, Japan, and Russia and assessed the evidence for intercontinental virus spread using phylogenetic methods. Additionally, we predicted viral virulence using deduced amino acid residues for the fusion protein cleavage site and estimated mutation rates for the fusion gene of class I and class II migratory bird isolates. All 73 isolates sequenced as part of this study were most closely related to virus genotypes previously reported for wild birds; however, five class II genotype I isolates formed a monophyletic clade exhibiting previously unreported genetic diversity, which met criteria for the designation of a new sub-genotype. Phylogenetic analysis of wild-bird isolates provided evidence for intercontinental virus spread, specifically viral lineages of APMV-1 class II genotype I sub-genotypes Ib and Ic. This result supports migratory bird movement as a possible mechanism for the redistribution of APMV-1. None of the predicted deduced amino acid motifs for the fusion protein cleavage site of APMV-1 strains isolated from migratory birds in Alaska, Japan, and Russia were consistent with those of previously identified virulent viruses. These data therefore provide no support for these strains contributing to the emergence of avian pathogens. The estimated mutation rates for fusion genes of class I and class II wild-bird isolates were faster than those reported previously for non-virulent APMV-1 strains. Collectively, these findings provide new insight into the diversity, spread, and evolution of APMV-1 in wild birds.
禽流感病毒血清型 1(APMV-1),也称为新城疫病毒,是引起新城疫的病原体,这是全球家禽养殖业中最重要的经济疾病之一,也是北美野生鸟类中周期性爆发的原因之一。在这项研究中,我们检查了从阿拉斯加、日本和俄罗斯采集的候鸟中分离出的 APMV-1 的遗传多样性,并使用系统发育方法评估了洲际病毒传播的证据。此外,我们使用融合蛋白裂解位点的推断氨基酸残基预测了病毒的毒力,并估计了 I 类和 II 类候鸟分离株融合基因的突变率。本研究中测序的 73 个分离株与先前报道的野生鸟类病毒基因型最为密切相关;然而,五个 II 类 I 型基因型分离株形成了一个单系分支,表现出以前未报道的遗传多样性,符合新亚基因型指定的标准。野生鸟类分离株的系统发育分析为洲际病毒传播提供了证据,特别是 APMV-1 II 类 I 型亚基因型 Ib 和 Ic 的病毒谱系。这一结果支持候鸟迁徙可能是 APMV-1 重新分布的一种机制。从阿拉斯加、日本和俄罗斯的候鸟中分离出的 APMV-1 株的融合蛋白裂解位点预测推断的氨基酸基序与先前确定的毒力病毒不一致。因此,这些数据并没有支持这些菌株导致禽病原体出现。I 类和 II 类野生鸟类分离株融合基因的估计突变率比以前报道的非毒力 APMV-1 株的突变率更快。总的来说,这些发现为了解野生鸟类中 APMV-1 的多样性、传播和进化提供了新的见解。