Channel catfish virus (CCV, Ictalurid herpesvirus 1) and CCV disease have been extensively studied. Yet, little is known about CCV-host interaction after resolution of the primary infection. In order to determine potential recrudescence of CCV from latency, we established latency by exposing channel catfish juveniles with CCV or a thymidine kinase-negative recombinant (CCVlacZ) at a dose that caused less than 20% mortality. Then, we evaluated antibody response by serially sampling the same fish at 0 (pre-infection), 30, 60 and 90 d post challenge (DPC). We then attempted to induce viral recrudescence by intramuscular administration of dexamethasone and sampled the fish at 2, 4, 7, or 10 d post treatment. Recrudescence was evaluated by leukocyte co-cultivation and cell culture of tissue homogenates but no virus was detected. Western blot data demonstrated the highest number of seropositive fish by 30 DPC and a secondary antibody induction after dexamethasone treatment. The antigen specificity of the secondary response corresponded to viral proteins with molecular masses similar to those recognized by the same fish by 30 DPC. The recognized proteins were predominantly large, ranging from ~90 to > 200 kDa. Expression analysis of selected virus genes at 90 DPC and following dexamethasone treatment demonstrated occasional immediate-early virus gene expression in peripheral blood leukocytes. Early and late gene expression was rarely detected. The combined data suggest restricted re-activation of CCV in our experimental system. Primary and secondary responses and virus gene expression were demonstrated in CCVlacZ-exposed fish but were less frequent than in CCV-exposed fish.KEY WORDS: Ictalurus punctatus · Teleost · Ictalurid herpesvirus 1 · Alloherpesviridae · Herpesvirus latency · Thymidine kinase-negative recombinant · Viral gene expression · Neutralizing antibody
Resale or republication not permitted without written consent of the publisherDis Aquat Org 95: [189][190][191][192][193][194][195][196][197][198][199][200][201] 2011 plex type 1 (HSV-1, Human herpesvirus 1), is characterized by expression of immediate-early (IE), early (E), and late (L) classes of viral genes in an ordered lytic cascade that culminates in the replication and packaging of viral DNA into infectious particles, and eventual lysis of the infected cells (Honess & Roizman 1974). With respect to the kinetics of gene expression, Dixon & Farber (1980) observed similar cascade regulation of the synthesis of 3 distinct classes of CCV proteins.Basic components of the morphology, biology, and genomic structure of CCV (Wolf & Darlington 1971, Plumb & Gaines 1975, Chousterman et al. 1979, Davison 1992 have been characterized since this fish herpesvirus was first isolated by Fijan (1968). CCV encodes thymidine kinase (TK), which phosphorylates thymidine and other deoxynucleotides and analogs (Hanson & Thune 1993). For HSV-1, TK is not required for growth in cell culture but is essential for virulence (Jamieson et al. 1974, Field & Wildy 1978, ...