Protective immunity against spring viremia of carp virus by mannose modified chitosan loaded DNA vaccine.

Virus Res

College of Animal Science and Technology, Northwest A&F University, Xinong Road 22nd, Yangling, Shaanxi 712100, China. Electronic address:

Published: October 2022

AI Article Synopsis

  • A study investigated a new DNA vaccine (CS-M-G) using mannose-modified chitosan to combat Spring viremia of carp virus (SVCV) in aquaculture.
  • The vaccine demonstrated effective immune response, showing significant antibody levels and persistent antigen expression post-vaccination.
  • Results indicated that the CS-M-G vaccine provided a high survival rate of 62.1% against SVCV, suggesting its potential for developing future aquatic vaccines.

Article Abstract

Spring viremia of carp virus (SVCV) usually be considered as one of the serious in viral diseases of aquaculture, and DNA vaccine with novel delivery mechanism or adjuvant has proven to be a promising and effective strategy to control aquatic animal diseases. In this study, the mannose-modified chitosan, a carrier system for vaccine delivery, were used to developed a chitosan-encapsulated DNA vaccine (CS-M-G) against SVCV, then investigated immune response induced by the vaccine. Our results showed that CS-M-G was confirmed the spherical or elliptical with even distribution and ranging from approximately 50 to 150 nm in size, the expression of the antigen gene could still be detected after 21 d post vaccination. The CS-M-G induces the highest antibody levels in the 20 μg dose group which is about 3 times than naked plasmid group at 21 d post vaccination, and still hold a higher level than control group at 28 d post vaccination. On the side, strongest protection with relative percent survival of 62.1% in the 20 μg CS-M-G group, which could produce significantly higher enzyme activities and up-regulated expression of immune-associated genes than control group. Thus, our results indicate that DNA vaccine loaded with mannose-modified chitosan induces strong immune response and provided an effective protection against SVCV infection, may be helpful and extended for developing more aquatic animal vaccines in the future.

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Source
http://dx.doi.org/10.1016/j.virusres.2022.198896DOI Listing

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