4.7 Article

Evaluation of an oral DNA nanovaccine against photobacteriosis in Solea senegalensis

期刊

FISH & SHELLFISH IMMUNOLOGY
卷 117, 期 -, 页码 157-168

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.fsi.2021.07.023

关键词

Photobacteriosis; Solea senegalensis; Oral DNA nanovaccine; Chitosan nanoparticles; Immune response

资金

  1. European Maritime and Fisheries Fund 2014-2020 within the Operational Programme for Spain [PP.FEM.PPA201700.9]

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Infectious diseases are a major cause of social and economic losses in world aquaculture, with bacterial diseases such as photobacteriosis impacting the production of Senegalese sole. This study aimed to develop an oral DNA nanovaccine for S. senegalensis juveniles against Photobacterium damselae subsp. piscicida (Phdp). The results indicate that oral vaccination with CS-TPP+pPDPimpdh NPs may be acting through non-specific immune responses as well as specific humoral and cell mediated immunity, providing a promising step towards developing an oral DNA nanovaccine against Phdp in sole.
Infectious diseases are one of the main causes of social and economical losses in world aquaculture. Senegalese sole (Solea senegalensis) is an important species for aquaculture in southern Europe, whose production is affected by the appearance of bacterial diseases such as photobacteriosis, a septicemia caused by Photobacterium damselae subsp. piscicida (Phdp). The aim of this study was to obtain an oral DNA nanovaccine and to evaluate its efficacy against Phdp in S. senegalensis juveniles. For this purpose, the amplified product corresponding to the protein inosine-5 '-monophophate dehydrogenase (IMPDH) from Phdp, was cloned into the expression vector pcDNATM6.2/C-EmGFP-GW obtaining the DNA vaccine named as pPDPimpdh. The correct transcription and protein expression was verified at 48 h post tansfection in HEK293 cells. Chitosan nanoparticles (CS-TPP NPs) were prepared by ionotropic gelation and their features were appropriate for use as oral delivery system. Therefore, pPDPimpdh was protected with chitosan CS-TPP NPs throughout complex coacervation method giving as a result a DNA nanovaccine referred as CS-TPP+pPDPimpdh NPs. Sole juveniles were vaccinated orally with CS-TPP NPs, pPDPimpdh and CS-TPP+pPDPimpdh NPs followed by a challenge with Phdp at 30 days post vaccination (dpv). The relative percentage survival (RPS) for pPDPimpdh vaccinated groups was 6.25%, probably due to its degradation in the digestive tract. RPS value obtained for CS-TPP NPs and CS-TPP+pPDPimpdh NPs was 40% and antibodies were observed in both cases. However, a delay in mortality was observed in sole juveniles vaccinated orally with CS-TPP+pPDPimpdh NPs. In fact, an upregulation of tf, mhcII, cd8a and igm in the posterior gut and c3, hamp1, tf and cd4 in spleen was observed in juveniles vaccinated with CSTPP+pPDPimpdh NPs. After challenge, a modulation of cd8a and cd4 expression levels in the posterior gut and c3, tf, lyg, cd4, igm and igt expression levels in spleen was observed. Moreover, the concentration of lysozyme in skin mucus significantly increased in fish vaccinated orally with CS-TPP+pPDPimpdh NPs at 11 dpc. These data indicate that oral vaccination with CS-TPP+pPDPimpdh NPs could be acting through the non-specific immune responses as well as the specific humoral and cell mediated immunity and provide the first step toward a development of an oral DNA nanovaccine against Phdp in sole.

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