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Whole-Body Analysis of a Viral Infection: Vascular Endothelium is a Primary Target of Infectious Hematopoietic Necrosis Virus in Zebrafish Larvae

机译:病毒感染的整体分析:血管内皮细胞是斑马鱼幼虫中感染性造血坏死病毒的主要目标

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摘要

The progression of viral infections is notoriously difficult to follow in whole organisms. The small, transparent zebrafish larva constitutes a valuable system to study how pathogens spread. We describe here the course of infection of zebrafish early larvae with a heat-adapted variant of the Infectious Hematopoietic Necrosis Virus (IHNV), a rhabdovirus that represents an important threat to the salmonid culture industry. When incubated at 24°C, a permissive temperature for virus replication, larvae infected by intravenous injection died within three to four days. Macroscopic signs of infection followed a highly predictable course, with a slowdown then arrest of blood flow despite continuing heartbeat, followed by a loss of reactivity to touch and ultimately by death. Using whole-mount in situ hybridization, patterns of infection were imaged in whole larvae. The first infected cells were detectable as early as 6 hours post infection, and a steady increase in infected cell number and staining intensity occurred with time. Venous endothelium appeared as a primary target of infection, as could be confirmed in fli1:GFP transgenic larvae by live imaging and immunohistochemistry. Disruption of the first vessels took place before arrest of blood circulation, and hemorrhages could be observed in various places. Our data suggest that infection spread from the damaged vessels to underlying tissue. By shifting infected fish to a temperature of 28°C that is non-permissive for viral propagation, it was possible to establish when virus-generated damage became irreversible. This stage was reached many hours before any detectable induction of the host response. Zebrafish larvae infected with IHNV constitute a vertebrate model of an hemorrhagic viral disease. This tractable system will allow the in vivo dissection of host-virus interactions at the whole organism scale, a feature unrivalled by other vertebrate models.
机译:众所周知,在整个生物体中,病毒感染的进展非常困难。小而透明的斑马鱼幼虫构成了一个有价值的系统,用于研究病原体如何传播。我们在这里描述了斑马鱼早期幼虫的热适应过程,即传染性造血坏死病毒(IHNV)的变种,它是对鲑鱼养殖业构成重要威胁的弹状病毒。在病毒复制的允许温度24℃下孵育时,经静脉注射感染的幼虫在三到四天内死亡。感染的宏观体征遵循高度可预测的过程,尽管心律持续不断,但速度减慢,然后停止血流,随后失去触摸反应性,最终导致死亡。使用整个原位杂交,感染模式成像在整个幼虫。最早的感染细胞早在感染后6小时就可以检测到,并且感染细胞数量和染色强度随时间稳定增长。静脉内皮似乎是感染的主要目标,可以通过实时成像和免疫组织化学在fli1:GFP转基因幼虫中证实。第一批血管破裂是在血液循环停止之前发生的,并且在各个地方都可以观察到出血。我们的数据表明感染从受损的血管扩散到下面的组织。通过将受感染的鱼转移到不允许病毒繁殖的28°C温度下,可以确定何时病毒产生的损害变得不可逆转。在任何可检测到的宿主反应诱导之前许多小时达到了此阶段。感染了IHNV的斑马鱼幼虫构成了出血性病毒疾病的脊椎动物模型。这种易于处理的系统将允许在整个生物体范围内对​​宿主病毒相互作用进行体内解剖,这是其他脊椎动物模型所无法比拟的。

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