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Ranaviruses are emerging pathogens associated with worldwide epizootics in farmed and wild ectothermic vertebrates. In this study, we determined the full genomes of eight ranaviruses isolated from marbled sleeper goby ( Oxyeleotris marmorata), goldfish ( Carassius auratus), guppy ( Poecilia reticulata), tiger frog ( Hoplobatrachus tigerinus), Asian grass frog ( Fejervarya limnocharis), and East Asian bullfrog ( H. rugulosus) cultured or imported into Thailand. These ranaviral isolates induced the same cytopathic effects (i.e., progression of coalescing round plaques) in epithelioma papulosum cyprini (EPC) cell cultures. Transmission electron microscopy of infected EPC cells revealed cytoplasmic viral particles with ultrastructural features typical for ranaviruses. Pairwise genetic comparisons of the complete major capsid protein coding sequences from the Thai ranaviruses displayed the highest identity (99.8%–100%) to a ranavirus (tiger frog virus; TFV) isolated from diseased tiger frogs cultured in China, a slightly lower identity (99.3%–99.4%) to a ranavirus (Wamena virus; WV) isolated from diseased green tree pythons ( Morelia viridis) illegally exported from Papua New Guinea, and a lower identity to 35 other ranaviruses (93.7%–98.6%). Phylogenomic analyses supported the eight Thai ranaviruses, Chinese TFV, and WV as a subclade within a larger frog virus 3 clade. Our findings confirm the spread of TFV among cultured fish and amphibians in Asia and likely in reptiles in Oceania. Biosecurity measures are needed to ensure TFV does not continue to spread throughout Southeast Asia and to other parts of the world via international trade.

The 149,343-bp genome of silurid herpesvirus 1, which was isolated in Thailand from glass catfish, was sequenced. The genome was most closely related to that of ictalurid herpesvirus 2, which infects black bullhead catfish. To our knowledge, this was the first silurid catfish alloherpesvirus genome to be sequenced.

Five immunostimulants were injected intraperitoneally into striped snakeheads (Channa striata). The inhibitory effects of the serum and macrophages collected from the treated fish on the germination and subsequent growth of Aphanomyces invadans (=piscicida), the causative agent of epizootic ulcerative syndrome (EUS), were then assessed. Salar-bec, a vitamin premix, and Ergosan, an alginate, both stimulated the inhibitory effects of serum on the germination and subsequent growth of A. invadans cysts, and the inhibitory effect of macrophages on growth. Betamak C85, a yeast extract containing β glucans and mannans, and Lysoforte, a lysophospholipid biosurfactant, induced little or no improvement in the parameters measured. Oro glo layer dry, a xanthophyll preparation, was rejected because of high mortalities among injected fish. Salar-bec showed the greatest improvement in the inhibition of both germination and growth by serum, and of growth by macrophages. It was selected for a tank trial in which snakeheads were fed on pellets coated with 2 g kg−1 Salar-bec, then injected with A. invadans. Control fish were fed on uncoated feed. Although the incidence of infection was not affected, hyphae appeared later in treated fish and granulomata developed faster at the infection site, suggesting an enhanced ability to contain the infection. Relative percent survival of treated fish was 59.2% higher than the controls over the 40-day trial. Anti-A. invadans antibody concentration was higher in treated fish, which may also have contributed to the containment of the infection.