• Korean Journal of Veterinary Research
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• v.43 no.3
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• pp.449-456
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• 2003

The VP2 gene of aquatic birnavirus, Korean isolate (GC-1) was cloned and expressed using the baculovirus expression system. The VP2 gene and VP2 partial gene, which contained a neutralizing epitope, were constructed for recombinant transfer vectors, for baculovirus expression. The expressed recombinant proteins were confirmed by indirect immuno fluorescence antibody (IFA), SDS-PAGE and Western blot. The level of expression was checked at regular time using IFA and Western blot. To measure the neutralizing activity of recombinant proteins against GC-1 strain, the antisera against recombinant proteins were produced by using guinea pigs. The result showed that the antisera neutralized the GC-1 strain. However, the neutralizing titer was higher in antisera against the VP2 gene expressed recombinant protein than that of VP2 partial gene recombinant protein.

• Journal of fish pathology
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• v.34 no.1
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• pp.17-22
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• 2021

Eukaryotic translation is initiated by either cap-dependent or cap-independent way, and the cap-independent translation can be initiated by the internal ribosomal entry site (IRES). In this study, to know whether the 5'UTR leader sequence of marine birnavirus (MABV) segment A and segment B can act as IRES, bicistronic vectors harboring a CMV promoter-driven red fluorescent gene (mCherry) and poliovirus IRES- or MABV's leader sequence-driven green fluorescent gene (eGFP) were constructed, then, transfected into a mammalian cell line (BHK-21 cells) and a fish cell line (CHSE-214 cells). The results showed that the poliovirus IRES worked well in BHK-21 cells, but did not work in CHSE-214 cells. In the evaluation of MABV's leader sequences, the reporter eGFP gene under the 5'UTR leader sequence of MABV's segment A was well-translated in CHSE-214 cells, indicating 5'UTR of MABV's segment A initiates translation in the cap-independent way and can be used as a fish-specific IRES system. However, the 5'UTR leader sequence of MABV's segment B did not initiate translation in CHSE-214 cells. As the precise mechanism of birnavirid IRES-mediated translation is not known, more elaborate investigations are needed to uncover why the leader sequence of segment B could not initiate translation in the present study. In addition, further studies on the host species range of MABV's segment A IRES and on the screening of other fish-specific IRESs are needed.

• Fisheries and Aquatic Sciences
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• v.3 no.1
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• pp.49-51
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• 2000

This study was performed to confirm the relationship between viral propagation and apoptosis by the infection of marine birnavirus strain (MABV NF-4) on chinook salmon embryo (CHSE-214) cells. After 6 hr viral infection, MABV was detected by PCR method. Also, as a result of DNA assay on the cells, MABV infection resulted in a typical feature of apoptosis, DNA fragmentation. The results suggest that MABV replicated to high concentrations during the early stage of infection induces apoptosis.

• Journal of fish pathology
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• v.11 no.2
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• pp.89-96
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• 1998

Marine birnavirus (MABV) has wide host range in marine organisms. To clarify various infection properties of MABV in different host species, in vitro study was performed by subculture for 10 passages in several fish cell lines. In CHSE-214, RTG-2 and RSBK-2 cells, the virus produced high yield of virus. Typical CPE with high protein expression was observed in these cells. On the contrary, the virus grown in EPC, FHM and BF-2 cells exhibited no CPE appearance although virus protein was detected. In EPC and FHM cells, the virus titer increased in later passages. The plaque size was distinctly bigger in CHSE-214, RTG-2 and RSBK-2 cells than in other cell lines. The nucleotide sequence of VP2/NS junction region on genome segment A exhibited one specific nucleotide change at 195. The different infection properties in several cell types performed in the present work might reflect in vivo MABV infection in various host species occurring in natural conditions.

• Proceedings of the Korean Society of Fisheries Technology Conference
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• 2000.05a
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• pp.438-439
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• 2000

지금까지의 연구에서 한국산 넙치 치어에서 분리된 버나바이러스는 MABV (Marine Birnavirus)와 혈청학적으로 유사하며, VP2/NS 경계영역의 염기배열도 MABV와 높은 homology를 가지고 있음을 밝혔다. 본 연구에서는 genome segment A를 중심으로 한국의 넙치에서 분리된 버나바이러스의 유전자해석을 행했다. (중략)

• Journal of fish pathology
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• v.8 no.2
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• pp.91-98
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• 1995

During 1993 and 1994, some mortalities of flounder(Paralichthy olivaceus) fry were recorded in several fish farms and viruses were isolated from 3 of the farms. Electron microscopic examination revealed that the virus particles were hexagonal and unenveloped with an average diameter of 50 to 55nm. Serological and molecular properties of these isolates were examined. The viral RNA and polypeptides patterns on electrophoresis, as well as neutralization test results, showed that these isolates were birnaviruses and two were closely related to infectious pancreatic necrosis virus(IPNV) serotype AB and one was to IPNV serotype SP. This is the first isolation of birnaviruses from marine fish in Korea.

• Journal of Microbiology
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• v.38 no.4
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• pp.260-264
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• 2000

Reverse transcription (RT)-PCR and nested PCR methods (2-step PCR) were tested for their ability to detect marine birnavirus (MBV) in cultured rockfish, Sebastes schlegeli. One set of primers for RT-PCR was designed, based on a gene of infectious pancreatic necrosis virus (IPNV), and another set of primers for nested PCR was designed based on the VP2/NS junction region of MBV. This 2-step PCR method was specific for MBV and sensitivity was heightened when nested PCR was combined to RT-PCR. This 2-step PCR method was useful for detecting MBV not only in diseased fish, but also in asymptomatic fish. These results indicate that this 2-step PCR method is useful for detecting MBV in rockfish.

• Journal of fish pathology
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• v.10 no.2
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• pp.165-176
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• 1997

Water samples collected from marine fish culture system in Korea were compared for their capability to reduce the infectivity titers of HRV (rhabdovirus olivaceus), FBV(flounder birnavirus) and RVS(retrovirus of salmonid). In addition, interaction between viruses and microorganisms present in the rearing seawater was examined. The titer of HRV and RVS were reduced at $15^{\circ}C$ to less than detectable limits within 3 to 5 days using untreated samples of seawater. No reduction of infectivity was noted in bacteria-free water treated by filtration or autoclaving. Bacteria (Pseudomonas and Vibrio sp.) isolated from the water collected from a flounder culture system showed the inactivation activity of HRV.

• Proceedings of the Korean Society of Fisheries Technology Conference
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• 2002.05a
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• pp.511-512
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• 2002

• Proceedings of the Korean Society of Fisheries Technology Conference
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• 2000.05a
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• pp.440-441
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• 2000

1990년대에 들면서, 온수 양어장에서 버나바이러스(Birnavirus)성 아가미 질병인 2차새변 벽주세포 괴사증(일명: 아가미 점상출혈증)과는 그 증상에서 차이를 보이는 아가미 질병이 발생되었다. 새변의 울혈과 괴사 병변을 주로 나타내는 본 질병은 경우에 따라 가슴지느러미와 아가미 근접복부에 출혈상을 나타내기도 한다. 병어의 병리조직학적 관찰, 분리 바이러스의 생화학적 또는 전자현미경 관찰 및 감염실험을 통해 아가미 질병의 원인 바이러스로도 H. anguillae가 인정되었으므로 이에 그 연구내용을 보고한다. (중략)