Trout oral VP2 DNA vaccination mimics transcriptional responses occurring after infection with infectious pancreatic necrosis virus (IPNV)

被引:32
|
作者
Ballesteros, Natalia A. [2 ]
Rodriguez Saint-Jean, Sylvia S. [2 ]
Perez-Prieto, Sara I. [2 ]
Coll, Julio M. [1 ]
机构
[1] INIA, Dpto Biotecnol, Madrid 28040, Spain
[2] CSIC, Ctr Invest Biol, Dpto Microbiol Mol & Biol Infecc, Madrid 28040, Spain
关键词
Infectious pancreatic necrosis virus; VP2; Oral DNA vaccines; Trout; IPNV; SALMON SALMO-SALAR; INTERFERON-INDUCED GENES; RAINBOW-TROUT; ATLANTIC SALMON; ONCORHYNCHUS-MYKISS; HEAD-KIDNEY; MX PROTEIN; EXPRESSION; FISH; INDUCTION;
D O I
10.1016/j.fsi.2012.09.004
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
Time-course and organ transcriptional response profiles in rainbow trout Oncorhynchus mykiss were studied after oral DNA-vaccination with the VP2 gene of the infectious pancreatic necrosis virus (IPNV) encapsulated in alginates. The profiles were also compared with those obtained after infection with IPNV. A group of immune-related genes (stat1, ifn1, ifng, mx1, mx3, il8, il10, il11, il12b, tnf2, mhc1uda, igm and igt) previously selected from microarray analysis of successful oral vaccination of rainbow trout, were used for the RTqPCR analysis. The results showed that oral VP2-vaccination qualitatively mimicked both the time-course and organ (head kidney, spleen, intestine, pyloric ceca, and thymus) transcriptional profiles obtained after IPNV-infection. Highest transcriptional differential expression levels after oral vaccination were obtained in thymus, suggesting those might be important for subsequent protection against IPNV challenges. However, transcriptional differential expression levels of most of the genes mentioned above were lower in VP2-vaccinated than in IPNV-infected trout, except for ifn1 which were similar. Together all the results suggest that the oral-alginate VP2-vaccination procedure immunizes trout against IPNV in a similar way as IPNV-infection does while there is still room for additional improvements in the oral vaccination procedure. Some of the genes described here could be used as markers to further optimize the oral immunization method. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1249 / 1257
页数:9
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