Abstract

Cyprinid herpesvirus 2 (CyHV-2, species Cyprinid herpesvirus 2) causes severe mortality in ornamental goldfish, crucian carp (Carassius auratus), and gibel carp (Carassius gibelio). It has been shown that the genomic DNA of CyHV-2 could be detected in subclinical fish, which implied that CyHV-2 could establish persistent infection. In this study, the latency of CyHV-2 was investigated in the survival fish after primary infection. CyHV-2 genomic DNA was detected in multiple tissues of acute infection samples; however, detection of CyHV-2 DNA was significantly reduced in fish recovered from the primary infection on day 300 postinfection. No active viral gene transcription, such as DNA polymerase and ORF99, was detected in recovered fish. Following temperature stress, an increase of CyHV-2 DNA copy numbers and gene transcription were observed in tissues examined, which suggests that CyHV-2 was reactivated under stress. In addition, a cell line (GCBLat1) derived from the brain tissue from CyHV-2-exposed fish harbored CyHV-2 genome but did not produce infectious virions under normal culture conditions. However, CyHV-2 replication and viral gene transcription occurred when GCBLat1 cells were treated with trichostatin A (TSA) or phorbol 12-myristate 13-acetate (TPA). It suggests CyHV-2 can remain latent in vitro and can reactivate under stress condition.

Highlights

  • Cyprinid herpesvirus 2 (CyHV-2, species Cyprinid herpesvirus 2), known as herpesviral hematopoietic necrosis virus of goldfish (Carassius auratus), causes high mortality in the farmed ornamental goldfish crucian carp (Carassius carassius) and gibel carp (Carassius gibelio) [1]

  • Highlights > CyHV-2 established latency following primary infection. > CyHV-2 latency could be reactivated by temperature stress in vivo. > A novel cell line derived from the brain of gibel carp was established and denoted by GCBLat1. > The GCBLat1 cell line supports CyHV-2 latency and reactivation

  • The latently infected GCBLat1 can be reactivated and can produce infectious virions. This cell line offers an in vitro model to investigate the mechanism of latency and reactivation for CyHV-2

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Summary

Introduction

Cyprinid herpesvirus 2 (CyHV-2, species Cyprinid herpesvirus 2), known as herpesviral hematopoietic necrosis virus of goldfish (Carassius auratus), causes high mortality in the farmed ornamental goldfish crucian carp (Carassius carassius) and gibel carp (Carassius gibelio) [1]. Outbreaks of CyHV-2 in wild gibel carp were reported in natural water reservoirs in Hungary, Czech Republic, and Italy [2,3]. Acute infection of CyHV-2 often occurs at a water temperature range of 15–25 ◦C and causes necrosis of gill and hematopoietic organs [4]. Injection of a kidney homogenate from those subclinical fish can cause acute CyHV-2 infection and mortality in the naïve fish [7]. These studies implied that CyHV-2 could establish a persistent infection

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