Shaping our future: animal health in a global trading environment

Ireland is currently experiencing both the positive and negative effects of global trade in agricultural products. With increasing global competition, there is little doubt that Irish agricultural product must increasingly compete on the basis of quality, rather than price

Transcription of signal-3 cytokines, IL-12 and IFNalphaß, coincides with the timing of CD8alphaß up-regulation durinig viral infection of common carp (Cyprinus carpio L.)

Mammalian naïve CD8+ T cells are activated by antigen (signal 1) and CD28 costimulation (signal 2) to undergo several rounds of cell division, but programming for survival, effector function and memory requires a third signal that can be provided by IL-12 and/or type I interferons. Functional studies indicate that the route of antigen presentation and costimulation are conserved from fish to mammals. However, the potential of IL-12 and IFN¿ß to act as signal-3 cytokines in infections inducing a CTL response has not been examined in fish. We report the cloning of CD8¿ and CD8ß homologues, each present in duplicate copies and of two TCR-C¿ isoforms in European common carp. The identification of (cytotoxic) T cell marker sequences and the availability of sequences coding for the signal-3 cytokines in the same fish species, allowed us to investigate by RT-qPCR their kinetics of gene expression during viral and parasitic infection. Our results show that transcription of signal-3 cytokines occurred concomitantly with CD8¿ß up-regulation exclusively at 4 days post-primary viral infection. No regulation of IL-12 and IFN¿ß was observed after parasitic infection. Our data provide evidences for an evolutionary conservation of function for IL-12 and IFN¿ß to act as third signal during CTL activation. In addition, we suggest that a CD8¿2/ß1 and a p35p40b association could be the preferred combinations for the formation of a functional CD8 co-receptor and an IL-12p70 heterodimer during viral infection. The relevance of our findings to future vaccination strategies in fish is discussed

Transcription of signal-3 cytokines, IL-12 and IFNalphaß, coincides with the timing of CD8alphaß up-regulation durinig viral infection of common carp (Cyprinus carpio L.)

Mammalian naïve CD8+ T cells are activated by antigen (signal 1) and CD28 costimulation (signal 2) to undergo several rounds of cell division, but programming for survival, effector function and memory requires a third signal that can be provided by IL-12 and/or type I interferons. Functional studies indicate that the route of antigen presentation and costimulation are conserved from fish to mammals. However, the potential of IL-12 and IFN¿ß to act as signal-3 cytokines in infections inducing a CTL response has not been examined in fish. We report the cloning of CD8¿ and CD8ß homologues, each present in duplicate copies and of two TCR-C¿ isoforms in European common carp. The identification of (cytotoxic) T cell marker sequences and the availability of sequences coding for the signal-3 cytokines in the same fish species, allowed us to investigate by RT-qPCR their kinetics of gene expression during viral and parasitic infection. Our results show that transcription of signal-3 cytokines occurred concomitantly with CD8¿ß up-regulation exclusively at 4 days post-primary viral infection. No regulation of IL-12 and IFN¿ß was observed after parasitic infection. Our data provide evidences for an evolutionary conservation of function for IL-12 and IFN¿ß to act as third signal during CTL activation. In addition, we suggest that a CD8¿2/ß1 and a p35p40b association could be the preferred combinations for the formation of a functional CD8 co-receptor and an IL-12p70 heterodimer during viral infection. The relevance of our findings to future vaccination strategies in fish is discussed

Optimizing genomic prediction of host resistance to koi herpesvirus disease in carp

AbstractGenomic selection (GS) is increasingly applied in breeding programmes of major aquaculture species, enabling improved prediction accuracy and genetic gain compared to pedigree-based approaches. Koi Herpesvirus disease (KHVD) is notifiable by the World Organisation for Animal Health and the European Union, causing major economic losses to carp production. Genomic selection has potential to breed carp with improved resistance to KHVD, thereby contributing to disease control. In the current study, Restriction-site Associated DNA sequencing (RAD-seq) was applied on a population of 1,425 common carp juveniles which had been challenged with Koi herpes virus, followed by sampling of survivors and mortalities. Genomic selection (GS) was tested on a wide range of scenarios by varying both SNP densities and the genetic relationships between training and validation sets. The accuracy of correctly identifying KHVD resistant animals using genomic selection was between 8 and 18 % higher than pedigree best linear unbiased predictor (pBLUP) depending on the tested scenario. Furthermore, minor decreases in prediction accuracy were observed with decreased SNP density. However, the genetic relationship between the training and validation sets was a key factor in the efficacy of genomic prediction of KHVD resistance in carp, with substantially lower prediction accuracy when the relationships between the training and validation sets did not contain close relatives.</jats:p

Investigation of ornamental fish entering the EU for the presence of ranaviruses

A survey was performed on ornamental fish imported into the EU to detect viral agents belonging to the genus Ranavirus. The objective was to gain knowledge of the potential for these systemic iridoviruses to gain entry into the EU via international trade in ornamental fish. A total of 208 pooled samples, representing 753 individual fish, were tested. The samples included 13 orders and 37 families, originating from different countries and continents. Tissues from fish that died during or just after transport were collected and examined by standard virological techniques in epithelioma papulosum cyprini cells, by transmission electron microscopy and by PCR for the detection of the major capsid protein and DNA polymerase gene sequences of ranaviruses. Virus was isolated from nine fish species but ranavirus was not identified in those samples. The results suggest that ranaviruses are not highly prevalent in ornamental fish imported into the EU