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Growth characteristics of the novel goose parvovirus SD15 strain in vitro

机译:新型鹅细小病毒SD15株的体外生长特性

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Short beak and dwarfism syndrome (SBDS) was caused by novel goose parvovirus (NGPV)--a variant of goose parvovirus (GPV). Ducks infected with NGPV shows clinical signs including growth retardation and protrusion of the tongue from an atrophied beak. SBDS outbreak was first reported at the northern coastal provinces of China during 2015 and it was again reported in Sichuan, an inland province of China in 2016. The disease caused a huge economic loss in Chinese duck feeding industry. The SD15 strain of NGPV was isolated from liver and intestinal tract tissue samples of infected ducks. Real-time quantitative PCR (qPCR) was used to estimate viral load in embryonated eggs and cells infected with adapted virus. The data showed that duck embryo fibroblasts (DEFs) were permissive to NGPV, while goose embryo fibroblasts (GEFs) cells were not, and the copy numbers of SD15 in the allantoic fluid of infected eggs remained at 105.0–106.5 copies/ml. The adaption procession of the virus was determined via qPCR, and viral proliferation was detected through indirect fluorescent antibody assay (IFA) in DEFs. It was further determined that viral copy numbers peaked at 96?h post-inoculation (hpi), which is the best time to harvest the virus in DEFs. Cytotoxic effects and cell death were observed at 72 hpi in SD15 infected DEFs, yet SD15 did not induce apoptosis. The growth characteristics of SD15 strain of NGPV determined would be beneficial for further molecular characterization of these viruses and develop potential vaccines if required.
机译:短喙和矮人综合症(SBDS)是由新型鹅细小病毒(NGPV)引起的-新型鹅细小病毒(GPV)。被NGPV感染的鸭子表现出临床症状,包括生长迟缓和舌头从萎缩的喙中伸出。 SBDS疫情于2015年首次在中国北部沿海省份报告,2016年在中国内陆省份四川再次报告。该病在中国鸭饲料行业造成了巨大的经济损失。从感染鸭子的肝脏和肠道组织样本中分离出NGPV的SD15株。实时定量PCR(qPCR)用于估计胚胎卵和适应病毒感染的细胞中的病毒载量。数据显示,鸭胚成纤维细胞(DEFs)允许NGPV,而鹅胚成纤维细胞(GEFs)细胞不允许,感染卵尿囊液中SD15的拷贝数保持在105.0–106.5拷贝/ ml。通过qPCR确定病毒的适应过程,并通过DEF中的间接荧光抗体测定(IFA)检测病毒增殖。进一步确定,病毒拷贝数在接种后96小时(hpi)达到峰值,这是在DEF中收集病毒的最佳时间。在被感染SD15的DEF中,在72 hpi时观察到细胞毒性作用和细胞死亡,但SD15不会诱导细胞凋亡。确定的NGPV SD15菌株的生长特性将有利于这些病毒的进一步分子表征,并在需要时开发潜在的疫苗。

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