Yu Kexiang, Ma Xiuli, Sheng Zizhang, Qi Lihong, Liu Cunxia, Wang Dan, Huang Bing, Li Feng, Song Minxun
Institute of Poultry Science, Shandong Academy of Agricultural Sciences, Jinan, Shandong, China.
Department of Biochemistry and Molecular Biophysics, Columbia University, New York, New York, USA.
J Clin Microbiol. 2016 Aug;54(8):1999-2007. doi: 10.1128/JCM.03244-15. Epub 2016 May 18.
A recent epizootic outbreak, in China, of duck beak atrophy and dwarfism syndrome (BADS) was investigated using electron microscopic, genetic, and virological studies, which identified a parvovirus with a greater similarity to goose parvovirus (GPV) (97% protein homology) than to Muscovy duck parvovirus (MDPV) (90% protein homology). The new virus, provisionally designated GPV-QH15, was found to be antigenically more closely related to GPV than to MDPV in a virus neutralization assay. These findings were further supported by phylogenetic analysis showing that GPV-QH15 evolved from goose lineage parvoviruses, rather than from Muscovy duck- or other duck species-related parvoviruses. In all, two genetic lineages (GPV I and GPV II) were identified from the GPV samples analyzed, and GPV-QH15 was found to be closely clustered with two known goose-origin parvoviruses (GPVa2006 and GPV1995), together forming a distinctive GPV IIa sublineage. Finally, structural modeling revealed that GPV-QH15 and the closely related viruses GPVa2006 and GPV1995 possessed identical clusters of receptor-interacting amino acid residues in the VP2 protein, a major determinant of viral receptor binding and host specificity. Significantly, these three viruses differed from MDPVs and other GPVs at these positions. Taken together, these results suggest that GPV-QH15 represents a new variant of goose-origin parvovirus that currently circulates in ducklings and causes BADS, a syndrome reported previously in Europe. This new finding highlights the need for future surveillance of GPV-QH15 in poultry in order to gain a better understanding of both the evolution and the biology of this emerging parvovirus.
近期中国发生了鸭喙萎缩和侏儒症综合征(BADS)的 epizootic 疫情,运用电子显微镜、遗传学和病毒学研究方法进行了调查。研究发现一种细小病毒,与鹅细小病毒(GPV)的相似性(蛋白质同源性为 97%)高于与番鸭细小病毒(MDPV)的相似性(蛋白质同源性为 90%)。在病毒中和试验中,新病毒暂命名为 GPV-QH15,发现其抗原性与 GPV 的关系比与 MDPV 更为密切。系统发育分析进一步支持了这些发现,表明 GPV-QH15 是从鹅系细小病毒进化而来,而非从番鸭或其他鸭种相关的细小病毒进化而来。总共从分析的 GPV 样本中鉴定出两个遗传谱系(GPV I 和 GPV II),并且发现 GPV-QH15 与两种已知的鹅源细小病毒(GPVa2006 和 GPV1995)紧密聚类,共同形成一个独特的 GPV IIa 亚谱系。最后,结构建模显示 GPV-QH15 以及与之密切相关的病毒 GPVa2006 和 GPV1995 在 VP2 蛋白中具有相同的受体相互作用氨基酸残基簇,VP2 蛋白是病毒受体结合和宿主特异性的主要决定因素。值得注意的是,这三种病毒在这些位置与 MDPV 和其他 GPV 不同。综上所述,这些结果表明 GPV-QH15 代表一种新的鹅源细小病毒变体,目前在雏鸭中传播并导致 BADS,该综合征先前在欧洲有报道。这一新发现凸显了未来对家禽中 GPV-QH15 进行监测的必要性,以便更好地了解这种新兴细小病毒的进化和生物学特性。