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1.
Genome ; 61(1): 33-42, 2018 Jan.
Article in English | MEDLINE | ID: mdl-29035683

ABSTRACT

Little is known about the genetic architecture of traits important for salmonid restoration ecology. We mapped quantitative trait loci (QTL) using single nucleotide polymorphisms (SNPs) for juvenile body length, weight, shape, and vertical skin pigmentation patterns (parr marks) within three hybrid backcross families between European and North American subspecies of Atlantic salmon. Amounts of variation in skin colour and pattern quantified in the two second-generation transAtlantic families exceeded the ranges seen in purebred populations. GridQTL analyses using low-density female-specific linkage maps detected QTL showing experiment-wide significance on Ssa02, Ssa03, Ssa09, Ssa11, Ssa19, and Ssa26/28 for both length and weight; on Ssa04 and Ssa23 for parr mark number; on Ssa09 and Ssa13 for parr mark contrast; and on Ssa05, Ssa07, Ssa10, Ssa11, Ssa18, Ssa23, and Ssa26/28 for geometric morphometric shape coordinates. Pleiotrophic QTL on Ssa11 affected length, weight, and shape. No QTL was found that explained more than 10% of the phenotypic variance in pigmentation or shape traits. Each QTL was approximately positioned on the physical map of the Atlantic salmon genome. Some QTL locations confirmed previous studies but many were new. Studies like ours may increase the success of salmon restoration projects by enabling better phenotypic and genetic matching between introduced and extirpated strains.


Subject(s)
Quantitative Trait Loci , Salmo salar/genetics , Animals , Body Size/genetics , Body Weight/genetics , Chromosome Mapping , Crosses, Genetic , Female , Male , Phenotype , Polymorphism, Single Nucleotide , Salmo salar/anatomy & histology , Skin Pigmentation/genetics
2.
J Fish Dis ; 41(9): 1373-1384, 2018 Sep.
Article in English | MEDLINE | ID: mdl-29938793

ABSTRACT

The infectious salmon anaemia virus (ISAV) is capable of causing a significant disease in Atlantic salmon, which has resulted in considerable financial losses for salmon farmers around the world. Since the first detection of ISAV in Canada in 1996, it has been a high priority for aquatic animal health management and surveillance programmes have led to the identification of many genetically distinct ISAV isolates of variable virulence. In this study, we evaluated the virulence of three ISAV isolates detected in Atlantic Canada in 2012 by doing in vivo-controlled disease challenges with two sources of Atlantic salmon. We measured viral loads in fish tissues during the course of infection. Sequences of the full viral RNA genomes of these three ISAV isolates were obtained and compared to a high-virulence and previously characterized isolate detected in the Bay of Fundy in 2004, as well as a newly identified ISAV NA-HPR0 isolate. All three ISAV isolates studied were shown to be of low to mid-virulence with fish from source A having a lower mortality rate than fish from source B. Viral load estimation using an RT-qPCR assay targeting viral segment 8 showed a high degree of similarity between tissues. Through genomic comparison, we identified various amino acid substitutions unique to some isolates, including a stop codon in the segment 8 ORF2 not previously reported in ISAV, present in the isolate with the lowest observed virulence.


Subject(s)
Genome, Viral , Isavirus/genetics , Isavirus/pathogenicity , Orthomyxoviridae Infections/veterinary , Salmo salar/virology , Amino Acid Substitution , Animals , Canada/epidemiology , Codon, Terminator , Fish Diseases/epidemiology , Fish Diseases/virology , Genomics , Isavirus/isolation & purification , Orthomyxoviridae Infections/virology , Real-Time Polymerase Chain Reaction , Sequence Analysis, DNA , Viral Load , Virulence
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