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1.
J Fish Dis ; 39(3): 269-75, 2016 Mar.
Article in English | MEDLINE | ID: mdl-25832786

ABSTRACT

Spring viraemia of carp (SVC) is a rhabdovirus infection, which has a significant economic impact in pond cultures of carp in Europe and western Independent States of the former Soviet Union. The causative agent of SVC, spring viraemia of carp virus (SVCV), has been divided into four subgroups, Ia, Ib, Ic and Id, on the basis of glycoprotein (G) protein gene sequences. In this study, a new primer set was designed from a G gene sequence of SVCV to identify the four subtypes of SVCV by reverse transcription polymerase chain reaction (RT-PCR). The specific PCR products of 369 bp were amplified from 15 SVCV isolates of all four subtypes. However, pike fry rhabdovirus (PFRV), which is antigenically related to SVCV, and other viruses antigenically related to SVCV and PFRV were not amplified. The four subtypes of SVCV were specifically amplified by the RT-PCR. Furthermore, the detection limit of the RT-PCR was 7.1 × 10(2) copies/reaction, and it was not influenced by the addition of RNA extracted from fish tissues. The RT-PCR will be applied not only to RNA extracted from viral suspensions, but also from fish tissue. It will contribute to rapid identification of SVCV in fish with clinical signs of SVC.


Subject(s)
Aquaculture/methods , Fish Diseases/diagnosis , Rhabdoviridae Infections/veterinary , Vesiculovirus/genetics , Viremia/veterinary , Animals , Carps , Reverse Transcriptase Polymerase Chain Reaction , Rhabdoviridae Infections/diagnosis , Sensitivity and Specificity , Viremia/diagnosis
2.
J Fish Dis ; 38(8): 695-712, 2015 Aug.
Article in English | MEDLINE | ID: mdl-25073413

ABSTRACT

The pathogenesis of cyprinid herpesvirus-3 (CyHV-3) was studied using different lineages of carp/koi. After exposure to the virus, infected cells were first found in the skin by histopathology and by in situ hybridization. The epidermis of the skin was most severely damaged and often sloughed off in the fish sampled on days 5 through 8, and the fish that were highly sensitive to the virus died within 8 or 10 days after infection. Serum osmolality of the infected fish, particularly just before death, was significantly lower, suggesting that the osmotic shock consequent on the damage to the skin was the direct cause of the acute deaths. On the other hand, clinical and histopathological observations indicate that the carp of a less sensitive lineage most probably died of viral encephalitis around 3 weeks after infection. For these fish, the largest number of infected cells was found in the central nervous system (CNS) sampled on day 12. A substantial amount of viral genome was found in the CNS of carp surviving more than 1 year after the infection. Thus, the CNS is probably a major target for CyHV-3, and the virus can persistently infect the CNS, presumably establishing latency.


Subject(s)
Fish Diseases/pathology , Herpesviridae Infections/veterinary , Animals , Carps , Central Nervous System/pathology , Central Nervous System/virology , Chronic Disease , Epidermis/pathology , Fish Diseases/mortality , Genome, Viral , Herpesviridae/genetics , Herpesviridae/physiology , Herpesviridae Infections/mortality , Herpesviridae Infections/pathology , Kidney/pathology , Kidney/virology
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