Diseases of marine mammals can be difficult to diagnose because of the life history and protected status of these animals. Stranded marine mammals have been a particularly useful resource to discover and comprehend the diseases that plague these top predators.Additionally, advancements in high-throughput sequencing (HTS) has contributed to the discovery of novel pathogens in these animals. In this study, we use a combination of HTS and stranded harbor seals (Phoca vitulina) to better understand a known and unknown brain disease. To do this, we used transcriptomics to evaluate brain tissues from seven neonatal harbor seals that expired from an unknown cause of death (UCD) and compared them to four neonatal harbor seals that had confirmed phocine herpesvirus (PhV-1) infections in the brain. Comparing these two disease states we found that UCD animals showed a significant abundance of fatty acid metabolic transcripts in their brain tissue, thus we speculate that a fatty acid metabolic dysregulation contributed to the death of these animals. Furthermore, we were able to describe the response of four young harbor seals with PhV-1 infections in the brain. PhV-1 infected animals showed a significant ability to mount an innate and adaptive immune response, especially to combat viral infections.Our data also suggests that PhV-1 can hijack host pathways for DNA packaging and exocytosis. This is the first study to use transcriptomics in marine mammals to understand host and viral interactions and assess the death of stranded marine mammals with an unknown disease. Furthermore, we show the value of applying transcriptomics on stranded marine mammals for disease characterization.
14Diseases of marine mammals can be difficult to diagnose because of the life history and 15 protected status of these animals. Stranded marine mammals have been a particularly useful 16 resource to discover and comprehend the diseases that plague these top predators. Additionally, 17 advancements in high-throughput sequencing (HTS) has contributed to the discovery of novel 18 pathogens in these animals. In this study, we use a combination of HTS and stranded harbor seals 19 (Phoca vitulina) to better understand a known and unknown brain disease. To do this, we used 20 transcriptomics to evaluate brain tissues from seven neonatal harbor seals that expired from an 21 unknown cause of death (UCD) and compared them to four neonatal harbor seals that had 22 confirmed phocine herpesvirus (PhV-1) infections in the brain. Comparing these two disease 23 states we found that UCD animals showed a significant abundance of fatty acid metabolic 24 transcripts in their brain tissue, thus we speculate that a fatty acid metabolic dysregulation 25 contributed to the death of these animals. Furthermore, we were able to describe the response of 26 four young harbor seals with PhV-1 infections in the brain. PhV-1 infected animals showed a 27 significant ability to mount an innate and adaptive immune response, especially to combat viral 28 infections. Our data also sug...