Walleye epidermal hyperplasia virus

Phylogenetic analysis of the three confirmed Epsilonretroviruses shows they are related. After cloning techniques, sequence analysis determined that WEHV-1 and WEHV-2 are similar in size and share 95% amino acid identity in the pol region of reverse transcriptase. This finding suggests that they are different strains of the same virus or likely distinct species. The two types of WEHV also share over 80% of their amino acid sequence with the third member of the epsilonretrovirus genus. Included in this analysis was the observation of a homologous genomic organization in all three Epsilonretroviruses.[4]

Walleye epidermal hyperplasia lesions are characteristically broad, flat, translucent plaques that range in size (2–50 mm in diameter). Lesions are most often observed in sexually mature fish although transmission studies have shown that fingerling fish can be infected using cell-free virus components extracted from lesions. Multiple growths are also known to coalesce into larger lesions. Seasonal observations of the fish by scientists and sportsmen show a high incidence of the condition during the late fall, winter, and early spring months. Mortality in the host fish is hypothesized to be less related to the virus and more to secondary infections that invade necrotic tissue. These viruses have evolved a means to maintain a fine balance between its own proliferation and leaving behind a fit and reproductive host.[2]

As with other skin lesion retroviruses, the in-lake transmission of the WEHV particles appears to be the result of contact with water harboring released infectious viral particles or close contact with other fish. The infection proliferates in temperatures between 0–5 °C (32–41 °F), and this may be why it occurs primarily in the fall and spring. With this seasonal prevalence, it is suggested that an inverse relationship exists between water temperature and skin lesion size/abundance. This is especially evident in the fact that few walleye show signs of the condition during the summer months. The nature of the seasonality of this condition is linked to a couple possible hypotheses: (1) low water temperatures and immune suppression, and (2) the physiological stress associated with spring spawning It is important to note that this disease is not classified as zoonotic and is not known to infect humans.[5]

Molecular studies of retroviruses have been partly responsible for elucidating the mechanisms responsible for oncogenesis. The Epsilonretroviruses provide a unique model for understanding the development and regression of tumors due to its seasonal prevalence and genetic evolutionary baggage. Proteins encoded by these viruses function in cell cycle regulation, alteration of cell-signaling pathways to promote proliferation and suppression of host cell apoptosis, and induction of apoptosis. The genetic and transcriptional similarities of the three classified Epsilonrertovirus suggest that these viruses share homologous mechanisms to replicate and proliferate.[2][3]