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一种使用报告细胞系测量大西洋鲑鱼病毒血症指标的方法。

A method to measure an indicator of viraemia in Atlantic salmon using a reporter cell line.

机构信息

Marine Scotland Science, Marine Laboratory, Victoria Road, Aberdeen AB11 9DB, Scotland, UK.

出版信息

J Virol Methods. 2013 Aug;191(2):113-7. doi: 10.1016/j.jviromet.2013.04.009. Epub 2013 Apr 18.

Abstract

RTG-P1 is a transgenic fish cell line producing luciferase under the control of the IFN-induced Mx rainbow trout gene promoter. This cell line was used to measure viraemia of Salmonid alphavirus (SAV), the cause of Salmon Pancreas Disease (SPD), a serious disease in farmed Atlantic salmon. Two SAV genotype 1 (SAV1) isolates were used in this study, F93-125 (tissue-culture adapted, from Ireland) and 4640 (from a field case in Scotland). The kinetics and magnitude of luciferase activity were monitored versus the time of infection. During a direct infection experiment, the induction of luciferase significantly increased 16- and 4-fold after incubation for 6 days with F93-125 at 15 and 20°C, respectively. Filtration and heat treatment experiments demonstrated that the luciferase induction in RTG-P1 was dependent on viral replication. Unlike many cell lines used in fish viral diagnostic, RTG-P1 is not sensitive to salmonid serum, therefore, viraemia could be successfully monitored on serum collected from fish during a cohabitation challenge with 4640 isolate. A peak of viraemia could be detected 16 days post IP inoculation of the shedders. This novel cost-effective method to measure viraemia does not rely on development of cytopathic effect (CPE) in culture, is compatible with non-lethal blood collections in fish and can be used to assign emerging diseases to a viral aetiology.

摘要

RTG-P1 是一种转基因鱼类细胞系,在 IFN 诱导的虹鳟鱼 Mx 基因启动子的控制下产生荧光素酶。该细胞系用于测量鲑鱼甲肝病毒 (SAV) 的病毒血症,SAV 是养殖大西洋鲑鱼胰腺疾病 (SPD) 的病因,这是一种严重的疾病。本研究使用了两种 SAV 基因型 1 (SAV1) 分离株,F93-125(组织培养适应株,来自爱尔兰)和 4640(来自苏格兰的田间病例)。监测了感染时间与荧光素酶活性的动力学和幅度。在直接感染实验中,在 15 和 20°C 下用 F93-125 孵育 6 天后,荧光素酶的诱导显著增加了 16 倍和 4 倍。过滤和热处理实验表明,RTG-P1 中的荧光素酶诱导依赖于病毒复制。与鱼类病毒诊断中使用的许多细胞系不同,RTG-P1 对鲑鱼血清不敏感,因此可以成功监测与 4640 分离株同居挑战期间从鱼类采集的血清中的病毒血症。在 16 天的 IP 接种后,可以检测到病毒血症的峰值。这种新型经济有效的测量病毒血症的方法不依赖于培养中细胞病变效应 (CPE) 的发展,与鱼类非致死性血液采集兼容,可用于将新发疾病归因于病毒性病因。

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