Genome-Wide Association Analysis for Resistance to Infectious Pancreatic Necrosis Virus Identifies Candidate Genes Involved in Viral Replication and Immune Response in Rainbow Trout (Oncorhynchus mykiss)

Author:

Rodríguez Francisco H12ORCID,Flores-Mara Raúl13ORCID,Yoshida Grazyella M14ORCID,Barría Agustín1ORCID,Jedlicki Ana M1ORCID,Lhorente Jean P4ORCID,Reyes-López Felipe5ORCID,Yáñez José M16

Affiliation:

1. Facultad de Ciencias Veterinarias y Pecuarias, Universidad de Chile, 8820808, La Pintana, Santiago, Chile

2. Facultad de Medicina Veterinaria y Zootecnia, Universidad Nacional del Altiplano, Av. Floral 1153, Puno, Perú

3. Escuela Profesional de Medicina Veterinaria y Zootecnia, Facultad de Ciencias de la Salud, Universidad Andina Néstor Cáceres Velásquez, Juliaca, Puno, Perú

4. Benchmark Genetics Chile, Puerto Montt, Chile

5. Department of Cell Biology, Physiology and Immunology, Universitat Autònoma de Barcelona, 08193, Barcelona, Spain, and

6. Núcleo Milenio INVASAL, Concepción 4070386, Chile

Abstract

Abstract Infectious pancreatic necrosis (IPN) is a viral disease with considerable negative impact on the rainbow trout (Oncorhynchus mykiss) aquaculture industry. The aim of the present work was to detect genomic regions that explain resistance to infectious pancreatic necrosis virus (IPNV) in rainbow trout. A total of 2,278 fish from 58 full-sib families were challenged with IPNV and 768 individuals were genotyped (488 resistant and 280 susceptible), using a 57K SNP panel Axiom, Affymetrix. A genome-wide association study (GWAS) was performed using the phenotypes time to death (TD) and binary survival (BS), along with the genotypes of the challenged fish using a Bayesian model (Bayes C). Heritabilities for resistance to IPNV estimated using genomic information, were 0.53 and 0.82 for TD and BS, respectively. The Bayesian GWAS detected a SNP located on chromosome 5 explaining 19% of the genetic variance for TD. The proximity of Sentrin-specific protease 5 (SENP5) to this SNP makes it a candidate gene for resistance against IPNV. In case of BS, a SNP located on chromosome 23 was detected explaining 9% of the genetic variance. However, the moderate-low proportion of variance explained by the detected marker leads to the conclusion that the incorporation of all genomic information, through genomic selection, would be the most appropriate approach to accelerate genetic progress for the improvement of resistance against IPNV in rainbow trout.

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology

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