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首页> 外文期刊>Veterinary research >Low virulent infectious salmon anaemia virus (ISAV) replicates and initiates the immune response earlier than a highly virulent virus in Atlantic salmon gills
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Low virulent infectious salmon anaemia virus (ISAV) replicates and initiates the immune response earlier than a highly virulent virus in Atlantic salmon gills

机译:在大西洋鲑鱼腮中,低毒传染性鲑鱼贫血病毒(ISAV)比高毒力病毒更早复制并开始免疫反应

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Observations from the field and experimental evidence suggest that different strains of infectious salmon anaemia virus (ISAV) can induce disease of varying severity in Atlantic salmon. Variation in host mortality and dissemination of ISAV isolates with high and low virulence was investigated using immersion challenge; from which mortality, pathological, immunohistochemical and preliminary molecular results have been previously published. Here, real-time RT-PCR analysis and statistical modelling have been used to further investigate variation in virus load and the response of four select immune genes. Expression of type I and II interferon (IFN), Mx and γIFN induced protein (γIP) to high and low pathogenic virus infection were examined in gill, heart and anterior kidney. In addition, a novel RNA species-specific assay targeting individual RNA types was used to investigate the separate viral processes of transcription and replication. Unexpectedly, the low virulent ISAV (LVI) replicated and transcribed more rapidly in the gills compared to the highly virulent virus (HVI). Subsequently LVI was able to disseminate to the internal organs more quickly and induced a more rapid systemic immune response in the host that may have offered some protection. Contrary to this, HVI initially progressed more slowly in the gills resulting in a slower generalised infection. However HVI ultimately reached a higher viral load and induced a greater mortality.
机译:来自现场的观察和实验证据表明,不同种类的传染性鲑鱼贫血病毒(ISAV)可以在大西洋鲑鱼中诱发不同严重程度的疾病。使用浸没攻击研究宿主死亡率的变化以及高毒力和低毒力的ISAV分离株的传播。先前已发表了有关死亡率,病理学,免疫组化和初步分子结果的文章。在这里,实时RT-PCR分析和统计模型已被用来进一步研究病毒载量的变化和四个选择的免疫基因的反应。在g,心脏和前肾中检查了I型和II型干扰素(IFN),Mx和γIFN诱导的蛋白(γIP)对高致病性病毒感染和低致病性病毒感染的表达。此外,针对个体RNA类型的新型RNA物种特异性测定用于研究转录和复制的独立病毒过程。出乎意料的是,与高毒力病毒(HVI)相比,低毒力ISAV(LVI)在the中复制和转录更快。随后,LVI能够更快地传播到内部器官,并在宿主中诱导更快的全身免疫反应,这可能提供了一些保护。与此相反,HVI最初在the中的进展较慢,导致较慢的全身感染。但是,HVI最终达到了更高的病毒载量,并导致了更高的死亡率。

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