AI Article Synopsis

  • - Viral nervous necrosis (VNN) is a serious disease affecting European sea bass caused by a specific virus (RGNNV), particularly impacting young fish in aquaculture settings.
  • - To investigate genetic resistance to VNN, researchers tested 4,851 individuals from different year classes and identified relevant genetic markers through genome-wide association analysis, revealing important gene regions linked to disease resistance.
  • - The study found that genetic information provided better predictions for breeding values (20-43% more accurate) compared to traditional pedigree methods, highlighting the potential for improved breeding strategies in aquaculture.

Article Abstract

Viral nervous necrosis (VNN) is an infectious disease caused by the red-spotted grouper nervous necrosis virus (RGNNV) in European sea bass and is considered a serious concern for the aquaculture industry with fry and juveniles being highly susceptible. To understand the genetic basis for resistance against VNN, a survival phenotype through the challenge test against the RGNNV was recorded in populations from multiple year classes (YC2016 and YC2017). A total of 4,851 individuals from 181 families were tested, and a subset (n∼1,535) belonging to 122 families was genotyped using a ∼57K Affymetrix Axiom array. The survival against the RGNNV showed low to moderate heritability with observed scale estimates of 0.18 and 0.25 obtained using pedigree vs. genomic information, respectively. The genome-wide association analysis showed a strong signal of quantitative trait loci (QTL) at LG12 which explained ∼33% of the genetic variance. The QTL region contained multiple genes (, , , , , , ) with and/or genes being highly relevant with a likely effect on host response in managing disease-associated symptoms. The results on the accuracy of predicting breeding values presented 20-43% advantage in accuracy using genomic over pedigree-based information which varied across model types and applied validation schemes.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8992836PMC
http://dx.doi.org/10.3389/fgene.2022.804584DOI Listing

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