Abstract
Cutthroat trout virus (CTV) is a non-pathogenic fish virus belonging to the Hepeviridae family, and it is distantly related to hepatitis E virus (HEV). Here, we report the development of an efficient cell culture system where CTV can consistently replicate to titers never observed before with a hepevirus. By using the rainbow trout gill (RTGill-W1) cell line, CTV reaches 1010 geq/mL intracellularly and 109 geq/mL extracellularly within 5–6 days in culture. We additionally established a qPCR system to investigate CTV infectivity, and developed a specific antibody directed against the viral capsid protein encoded by ORF2. With these methods, we were able to follow the progressive accumulation of viral RNA and the capsid protein, and their intracellular distribution during virus replication. Virus progeny purified through iodixanol density gradients indicated—that similar to HEV—CTV produced in cell culture is also lipid-associated. The lack of an efficient cell culture system has greatly impeded studies with HEV, a major human pathogen that causes hepatitis worldwide. Although several cell culture systems have recently been established, the replication efficiency of HEV is not robust enough to allow studies on different aspects of the virus replication cycle. Therefore, a surrogate virus that can replicate easily and efficiently in cultured cells would be helpful to boost research studies with hepeviruses. Due to its similarities, but also its key differences to HEV, CTV represents a promising tool to elucidate aspects of the replication cycle of Hepeviridae in general, and HEV in particular.
Highlights
Cutthroat trout virus (CTV) was first isolated from spawning adult trout in 1988 [1]
It is likely that ORF3 encodes a phosphoprotein, which in hepatitis E virus (HEV) is required for budding and for the formation of lipid-associated progeny particles, which are observed in serum and cell culture supernatant (SN) [4]
We describe the development of a cell culture system where CTV replicates with an efficiency never before observed with HEV or with any other member of the Hepeviridae family, and the establishment of analytical tools to characterize the infection
Summary
Cutthroat trout virus (CTV) was first isolated from spawning adult trout in 1988 [1]. Based on the similarities to hepatitis E virus (HEV), CTV was classified as a member of the Hepeviridae family [2]. This family has been divided into two proposed genera, Orthohepevirus (all mammalian and avian HEV isolates) and Piscihepevirus (CTV) [3]. The location of ORF3 is similar to that of HEV genotype 4, where its 50 end does not overlap with ORF1. Upon pairwise alignment with HEV, it was shown that the nucleotide sequence identity of the 50 UTR is 44%, and that that of the 30 UTR is 40%.
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