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1.
Theriogenology ; 84(1): 170-6.e2, 2015 Jul 01.
Article in English | MEDLINE | ID: mdl-25896075

ABSTRACT

Modern out-of-season egg production in Atlantic salmon (Salmo salar) increases the risk of postovulatory aging (POA) of oocytes. Postovulatory aging is known to influence oocyte quality in salmonids, but reliable tests for POA are lacking in Atlantic salmon egg production. To address this problem, we have collected oocytes from the same 20 Atlantic salmon females sequentially in approximately 1-week intervals, from the start of ovulation until 28 days postovulation (dpo), to determine the effect of natural retention of matured oocytes in body coelomic cavity on further performance of embryos and juveniles produced from those oocytes. Also, we investigated oocyte water hardening and several coelomic fluid parameters as potential quantitative indicators of POA. Oocyte quality decreased significantly from 22 dpo onward, as inferred from decrease in fertilization success and survival of embryos, alevins, and juveniles and increase in alevin and juvenile deformity rates. The occurrence of head deformities was significantly related to postovulatory age of oocytes. Coelomic fluid pH decreased significantly at 28 dpo and correlated positively with fertilization rates (r = 0.45), normal eyed embryo rates (r = 0.67), and alevin relative survival rates (r = 0.63) and negatively correlated with total alevin deformity rates (r = -0.59). Oocyte weight gain at 60 minutes decreased significantly at 28 dpo and correlated negatively with total alevin deformities and the occurrence of cranial nodules (r = -0.99). Generally, quality of ovulated oocytes remained stable for the first 2 weeks after ovulation. Later on, POA negatively influenced Atlantic salmon embryo, alevin, and juvenile performance. For the first time, we show a long-term effect of POA on salmonid juvenile performance. Standardized pH measurements of coelomic fluid could potentially improve embryo and juvenile production by identifying low-quality oocytes at an early stage during the production.


Subject(s)
Cellular Senescence , Oocytes/cytology , Salmo salar/physiology , Animals , Embryo, Nonmammalian/cytology , Embryo, Nonmammalian/physiology , Hydrogen-Ion Concentration , Larva/growth & development , Oocytes/growth & development , Salmo salar/embryology , Salmo salar/growth & development , Seasons
2.
Fish Shellfish Immunol ; 31(1): 1-9, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21232605

ABSTRACT

Selective breeding has been employed to improve resistance to infectious diseases in aquaculture and it is of importance to investigate the expression profiles of immune genes together with complement activity of Atlantic salmon with different genetic background in response to pathogens, in particular against Aeromonas salmonicida. This study examined acute phase products, and several central T cell cytokines and a transcription factor in different tissues, namely head kidney, spleen and liver, in two families of Atlantic salmon with high and low mortalities, after challenge by A. salmonicida. The results showed that the expression pattern of target genes differed in lymphoid and non-lymphoid organs in the two families. Generally, in lymphoid organs, higher expression of pro-inflammatory genes, such as TLR5M, TLR5S, GATA3, IFN-γ, IL-17D, as well as the pleiotropic cytokine gene IL-10 in the resistant family was observed at the same time point. One may speculate that a relatively high immune response is a pre-requisite for increased survival in a A. salmonicida challenge test. In addition, the resistant fish possessed higher complement activity pre-challenge compared to susceptible fish. Complement activity may be applied as an indicator in selective breeding for enhanced disease resistance.


Subject(s)
Aeromonas salmonicida/immunology , Cytokines/genetics , Fish Diseases/genetics , Furunculosis/genetics , Gram-Negative Bacterial Infections/veterinary , Salmo salar/genetics , Transcription Factors/genetics , Animals , Base Sequence , Cytokines/immunology , Fish Diseases/immunology , Fish Diseases/microbiology , Fish Proteins/genetics , Fish Proteins/immunology , Furunculosis/immunology , Furunculosis/microbiology , Gene Expression , Gram-Negative Bacterial Infections/genetics , Gram-Negative Bacterial Infections/immunology , Gram-Negative Bacterial Infections/microbiology , Immunity, Innate , Kidney/immunology , Kidney/metabolism , Kidney/microbiology , Liver/immunology , Liver/metabolism , Liver/microbiology , Molecular Sequence Data , Salmo salar/immunology , Salmo salar/microbiology , Spleen/immunology , Spleen/metabolism , Spleen/microbiology , Transcription Factors/immunology
3.
Immunogenetics ; 55(4): 210-9, 2003 Jul.
Article in English | MEDLINE | ID: mdl-12811427

ABSTRACT

Few studies have yet addressed the functional aspects of MHC molecules in fish. To lay the foundation for this, we evaluated the association between disease resistance and MHC class I and class II polymorphism in Atlantic salmon. Standardized disease challenge trials were performed on a semi-wild Atlantic salmon population with subsequent MHC typing and statistical analysis. The pathogens employed were infectious salmon anaemia virus (ISAV) causing infectious salmon anaemia and the Aeromonas salmonicida bacteria causing furunculosis. The material consisted of 1,182 Atlantic salmon from 33 families challenged with A. salmonicida and 1,031 Atlantic salmon from 25 families challenged with ISAV. We found highly significant associations between resistance towards infectious diseases caused by both pathogens and MH class I and class II polymorphism in Atlantic salmon. The observed associations were detected due to independently segregating MH class I and class II single loci, and inclusion of a large number of fish allowing an extensive statistical analysis.


Subject(s)
Genes, MHC Class II , Genes, MHC Class I , Salmo salar/genetics , Salmo salar/immunology , Aeromonas/pathogenicity , Alleles , Animals , Fish Diseases/genetics , Fish Diseases/immunology , Gram-Negative Bacterial Infections/genetics , Gram-Negative Bacterial Infections/immunology , Gram-Negative Bacterial Infections/veterinary , Orthomyxoviridae/pathogenicity , Orthomyxoviridae Infections/genetics , Orthomyxoviridae Infections/immunology , Orthomyxoviridae Infections/veterinary , Polymorphism, Genetic , Quantitative Trait Loci , Salmo salar/microbiology , Salmo salar/virology
4.
Proc Biol Sci ; 269(1504): 2029-33, 2002 Oct 07.
Article in English | MEDLINE | ID: mdl-12396502

ABSTRACT

The extreme polymorphism found at some major histocompatibility complex (MHC) loci is believed to be maintained by balancing selection caused by infectious pathogens. Experimental support for this is inconclusive. We have studied the interaction between certain MHC alleles and the bacterium Aeromonas salmonicida, which causes the severe disease furunculosis, in Atlantic salmon (Salmo salar L.). We designed full-sibling broods consisting of combinations of homozygote and heterozygote genotypes with respect to resistance or susceptibility alleles. The juveniles were experimentally infected with A. salmonicida and their individual survival was monitored. By comparing full siblings carrying different MHC genotypes the effects on survival due to other segregating genes were minimized. We show that a pathogen has the potential to cause very intense selection pressure on particular MHC alleles; the relative fitness difference between individuals carrying different MHC alleles was as high as 0.5. A co-dominant pattern of disease resistance/susceptibility was found, indicative of qualitative difference in the immune response between individuals carrying the high- and low-resistance alleles. Rather unexpectedly, survival was not higher among heterozygous individuals as compared with homozygous ones.


Subject(s)
Aeromonas/immunology , Alleles , Gram-Negative Bacterial Infections/immunology , Major Histocompatibility Complex/genetics , Salmo salar/genetics , Salmo salar/immunology , Animals , Fish Diseases/immunology , Fish Diseases/microbiology , Gene Frequency , Genes, MHC Class II/genetics , Genetic Predisposition to Disease/genetics , Genetic Variation/genetics
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