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首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Bicistronic DNA vaccine macromolecule complexed with poly lactic-co-glycolic acid-chitosan nanoparticles enhanced the mucosal immunity of Labeo rohita against Edwardsiella tarda infection
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Bicistronic DNA vaccine macromolecule complexed with poly lactic-co-glycolic acid-chitosan nanoparticles enhanced the mucosal immunity of Labeo rohita against Edwardsiella tarda infection

机译:双函箱DNA疫苗大分子与聚乳酸 - 共乙醇酸 - 壳聚糖纳米粒子络合,增强了Labeo rohita的粘膜免疫性针对Edwardella tarda感染

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DNA vaccine is an important tool to elicit both humoral and cellular immunity. Present study investigates mucosal immune response of Labeo rohita (15 +/- 04 g) to plasmid DNA (pDNA) vaccine macromolecule complexed with nanoparticles (NPs). Poly lactic-co-glycolic acid (PLGA), Chitosan (Chit) and PLGA-Chit-NPs were synthesized by double emulsion solvent evaporation method. Synthesized NPs were complexed with pDNA (pGPD + IFN) vaccine construct. Size and zeta potential of PLGA-NPs, Chit-NPs and PLGA-Chit-NPs-pDNA complex were recorded to be 120 nm and +0.5 mV, 117 nm and +32 mV, 189 nm and +11 mV, respectively. Immunization by immersion was carried out in two groups receiving PLGA-Chit-NPs-pDNA (T1) and PLGA-NPs-pDNA (T2) respectively. After immersion, samples were collected on 0, 2, 4, 7, 15 and 30 days from mucosa-associated lymphoid tissues (MALT) for mRNA expression studies of IgM, IgD and IgZ using qRT-PCR. Significant up-regulation of the mRNA expression of IgM, IgD, and IgT were observed in MALT in immunized fish compared to control. After 30 days post-immunization fish were infected with a virulent strain of Edwardsiella tarda. The highest relative percentage survival was observed in T1 (64.7%) compared to T2. The study showed better efficiency of pDNA-PLGA-Chit-NPs compared to pDNA-PLGA-NPs for inducing adaptive mucosal immunity in fish. (C) 2020 Elsevier B.V. All tights reserved.
机译:DNA疫苗引起体液和细胞免疫的重要工具。南亚野鲮(15 +/-04克)的本研究调查粘膜免疫应答质粒与纳米颗粒(NP)复合的DNA(质粒DNA)疫苗大分子。聚乳酸 - 共 - 乙醇酸(PLGA),壳聚糖(捷)和PLGA-吹水纳米粒通过双乳液溶剂蒸发方法来合成。合成纳米粒子用质粒DNA(PGPD + IFN)疫苗构建复合。大小和PLGA-的NP,吹水纳米粒和PLGA-吹水-NPS-的pDNA复杂的ζ电位,记录分别为120纳米和0.5毫伏,117纳米和32毫伏,189纳米和11毫伏。通过浸入免疫接种是在两组接收PLGA-吹水-NPS-的pDNA(T1)和PLGA-NPS-分别的pDNA(T2)进行的。浸渍后,将样品收集在0,2,4,7,15和30天,从粘膜相关淋巴组织(MALT),用于使用qRT-PCR的IgM,IgD和IgZ的mRNA的表达的研究。在MALT未观察到免疫鱼的IgM,IgD和IGT的mRNA表达的显著上调与对照相比。 30天后免疫后的鱼被感染迟钝爱德华氏菌的毒力株。在T1相比T2(64.7%)中观察到最高的相对百分比存活。该研究显示,相较于质粒DNA-PLGA纳米粒在鱼适应性诱导粘膜免疫的质粒DNA-PLGA-吹水-NP的更好的效率。 (C)2020爱思唯尔B.V.所有紧身衣保留。

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