Moreover, in the spleen, both vaccines induced a significant reduction of CD4 levels at day 7 or 14. For CD8α, the find more IPNV vaccine had no significant effects on muscle and spleen, but significantly reduced CD8α mRNA levels at day 7 to then significantly increase them at day 14. By contrast, the VHSV vaccine strongly induced its levels in muscle and to a less extent in the head kidney, but significantly
reduced its levels in spleen. To assess the generation of specific antibodies, we evaluated the neutralizing capacity of serum from vaccinated fish 30 days post-vaccination (Table 2). Sera from empty plasmid vaccinated fish showed a very low neutralizing activity, (titers of 60 ± 10) comparable to sera obtained from untreated trout. IPNV DNA vaccination resulted in a significant increase in the neutralizing antibodies with titers up to 800 (mean titers of 443.75 ± 113.17). We evaluated the viral load through VP1 gene expression
after intraperitoneal injection of IPNV in control and pIPNV-PP see more vaccinated trout 30 days post-vaccination (Fig. 6). Very variable levels of virus were detected in the 5 PBS-injected fish. The injection with the empty plasmid resulted in a reduced viral load (27-fold) and IPNV was detected in 4 out of 5 fish. However, the viral load was considerably reduced in fish vaccinated with the pIPNV-PP construct (665-fold). In this case, IPNV was Non-specific serine/threonine protein kinase only detected in 1 out of 5 fish sampled. Outbreaks of IPNV are still one of the major problems caused
by viral diseases in modern aquaculture. Although some experimental vaccines have been developed so far, only a few have been commercialised, and the protective effect against IPNV demonstrated in laboratory trials are not consistent with field observations. This may, however, be due to the fact that in the field the fish may be exposed to several other pathogens in addition to IPNV. Every year, many Atlantic salmon fish farms and hatcheries (30–40%) have high mortalities due to IPNV outbreaks [7]. It has been speculated that this high impact of IPNV despite the availability of the vaccine in some countries could be due to the poor antigenic nature of the IPNV antigens produced in different expression systems, the difficulty to establish good challenge models for IPNV or that the vaccinated fish are already infected [8], [11], [12] and [13]. All this reminds us of the necessity for new and improved vaccines for early vaccination of salmonids before they naturally get infected with IPNV. In this sense, DNA vaccines are promising tools since they have been proved as very effective for fish rhabdovirus, reaching protection up to 100% and lasting more than 2 years [14] and [15].
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