Oloruntimehin Ezekiel S, Volodina Sofya I, Patraman Ivan V, Nadtochey Grigory A, Malogolovkin Alexander S
Molecular Virology Laboratory, Martsinovsky Institute of Medical Parasitology, Tropical and Vector-Borne Diseases, First Moscow State Medical University (Sechenov University), Trubetskaya 8, 119048, Moscow, Russia.
Federal Research Center - All-Russian Research Institute of Experimental Veterinary Medicine named after K.I. Skrjabin and Y. R. Kovalenko of the Russian Academy of Sciences, Ryazanskiy pr. 24/1, 109428, Moscow, Russia.
Arch Virol. 2024 Dec 8;170(1):4. doi: 10.1007/s00705-024-06188-z.
The disease caused by goose parvovirus (GPV) affects young goslings and ducks and leads to substantial losses for farmers due to high mortality rates, reaching 70-100% in naive flocks. Here, we present the results of a study focusing on the historical virulent GPV LIV-22 strain, which was isolated in the USSR in 1972. An attenuated GPV LIV-22 vaccine strain that was generated by continuous passaging in goose embryonic fibroblasts was also studied. Phylogenetic analysis placed both GPV LIV-22 strains in the classical GPV group, close to the vaccine and low-pathogenic strains. However, several individual changes in the GPV LIV-22 VP1 gene highlight the uniqueness of the evolution and adaptation mechanism of GPV LIV-22 strains. Transmission electron microscopy (TEM) revealed severe ultrastructural changes in goose hepatocytes and enterocytes as early as 24-48 h postinfection, confirming abrupt GPV pathogenesis. This description of some of the essential characteristics of the GPV LIV-22 virulent and vaccine strain will be useful for studying GPV evolution and molecular pathogenesis.
鹅细小病毒(GPV)引起的疾病会影响幼龄雏鹅和雏鸭,由于死亡率高,给养殖户造成重大损失,在未接触过该病毒的禽群中死亡率可达70%-100%。在此,我们展示了一项针对1972年在前苏联分离出的具有历史毒性的GPV LIV-22毒株的研究结果。还对通过在鹅胚成纤维细胞中连续传代产生的减毒GPV LIV-22疫苗株进行了研究。系统发育分析将两种GPV LIV-22毒株归入经典GPV组,与疫苗株和低致病性毒株相近。然而,GPV LIV-22 VP1基因中的几个个体变化突出了GPV LIV-22毒株进化和适应机制的独特性。透射电子显微镜(TEM)显示,早在感染后24-48小时,鹅肝细胞和肠细胞就出现了严重的超微结构变化,证实了GPV发病机制的突然性。对GPV LIV-22强毒株和疫苗株一些基本特征的描述将有助于研究GPV的进化和分子发病机制。