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Nanoliposomes encapsulating immunostimulants modulate the innate immune system and elicit protection in zebrafish larvae

机译:包封免疫刺激剂的纳米脂质体调节先天免疫系统并在斑马鱼幼虫中引出保护

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摘要

Here we present immunostimulant-loaded nanoliposomes (NLc) as a strategy to protect zebrafish larvae against bacterial infection. The NLc encapsulate crude lipopolysaccharide (LPS) from E. coli and polyinosinic:polycytidylic acid (Poly I:C), a synthetic analogue of viral dsRNA. Fluorescently-labeled NLc were ingested by zebrafish larvae 4 days post fertilization, when administrated by bath immersion, and accumulated in ;the intestine. RT-qPCR analysis showed the expression of innate immune related genes (tnf alpha, ill beta, nos2a, irfla and ptgs2a) was significantly upregulated at 48 h post NLc, treatment. A zebrafish larvae infection model for Aeromonas hydrophila was set up by bath immersion, achieving bacterial-dose-dependent significant differences in survival at day 5 post infection in both injured and non-injured larvae. Using this model, NI., protected non injured zebrafish larvae against an A. hydrophila lethal infection. In contrast, neither the empty nanoliposomes nor the mixture of immunostimulants could protect larvae against lethal challenges. Our results demonstrate that nanoliposomes could be further developed as an efficient carrier, widening the scope for delivery of other immunostimulants in aquaculture.
机译:在这里,我们将负载免疫增生的纳米脂质体(NLC)作为保护斑马鱼幼虫免受细菌感染的策略。 NLC从大肠杆菌和多胞苷(Polycyidylic)(Poly I:C)中包装来自大肠杆菌和多胞苷的粗脂多糖(LPS),是病毒DsRNA的合成类似物。当受精后4天通过浴浸,并积累的肠道,通过斑马鱼幼虫4天摄取荧光标记的NLC。 RT-QPCR分析显示在NLC后48小时内显着上调了先天免疫相关基因的表达(TNFα,IRβ,NOS2A,IRFLA和PTGS2A)。 Zebrafish幼虫感染模型通过浴浸来设立疏水液,在伤害和非伤害幼虫两次感染后的生存中取得的细菌剂量依赖性显着差异。使用此模型,Ni。,受到A.患有A.疏水症的非受伤的斑马鱼幼虫。相比之下,空纳米骨骺和免疫刺激剂的混合物都不能保护幼虫免受致命挑战。我们的结果表明,纳米脂质体可以进一步开发为有效的载体,扩大了水产养殖中其他免疫刺激剂的范围。

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