• 한국가금학회지
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• 제35권1호
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• pp.85-99
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• 2008

국내 육계 농장에서 avian reovirus의 감염 여부를 확인하기 위한 ELISA 검사법을 이용한 혈청 검사와 바이러스 분리 및 2개 농장에서 분리된 바이러스를 SPF 닭에 공격 접종하여 병원성을 확인한 결과, 다음과 같은 결론을 얻었다. 1. 1일령 육계 병아리에서 avian reovirus에 대한 모체이행 항체 역가 검사를 통하여 육용종계에서 avian reovirus에 대한 항체 보유 상태가 매우 다양하며, 이로 인해 후 대 병아리의 항체 수준도 매우 불균일하게 분포된다는 것을 알 수 있었다. 2. 육계에서 avian reovirus에 대한 모체 이행 항체 역가는 14일령 전에 대부분 소실되며, 그 이후 혈청 역가가 상승하는 것이 확인되어 국내 육계 농장에서도 avian reovirus가 감염이 되는 것을 확인할 수 있었으며, 각 농장의 감염 상황 및 계군의 면역 정도에 따라 혈청 역가가 다양하게 분포함을 알 수 있었다. 3. RT-PCR을 이용한 avian reovirus 확인 결과, 1일령 병아리에서 모두 음성으로 확인되었고, 14일령과 출하 일령에 2개 농장에서 양성으로 나타나, 국내 육계 농장에서 avian reovirus 감염은 주로 14일령 이후에 나타나는 것으로 판단되었다. 4. 본 실험에서 실시한 ELISA, RT-PCR, 전자현미경 관찰을 통하여 국내 육계 농가에서의 ARV 감염과 존재를 확인할 수 있었다. 그러나 검사 방법간의 결과가 불일치한 것은 avian reovirus의 분리가 감염된 농장의 상황, 닭의 감염 일령 및 분리 장기에 따라 차이가 있음을 알 수 있었다. 5. 9일령 SPF 부화란 접종을 통해 2개의 육계 농장에서 avian reovirus가 분리되었고 분리된 바이러스를 3주령 SPF 닭에 공격 접종 시 혈청 역가의 상승 및 주요 조직에서 바이러스가 확인되었으나, 특이적인 임상 증상은 관찰되지 않았다. 이는 닭의 연령에 따라 avian reovirus에 저항성이 있는 것으로 여겨지며 ARV의 조직 내 잔존은 감염 장기에 따라 다르다는 것을 알 수 있었다.

• 한국동물위생학회지
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• 제42권4호
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• pp.237-243
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• 2019

Avian reovirus (ARV) is the pathogenic agent of tenosynovitis and malabsorption syndrome in broiler, which has caused significant economical losses due to poor feeder efficiency and stunting. In order to determine the prevalence of ARV infection in poultry farms in Jeonbuk province, Korea, we performed a surveillance study by testing 179 cecal samples from 131 broiler farms for virus detection, and 1,181 serum samples from 33 broiler farms (n=292) and 22 broiler breeder farms (n=1,525) for antibody detection in the province. Virological examination using RT-PCR showed that ARV were detected in 26.0% of the tested farms (34/131),with the highest positive rates in broilers of 6 days old or more in summer season. In serological test using ELISA, broiler and broiler breeder farms examined were all ARV antibody positive. In broiler, the positive rate and antibody titers showed a tendency to decrease with age in contrast to those of broiler breeders. Our results indicate that ARV is ubiquitous in broilers and broiler breeders in the province.

• 한국동물위생학회지
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• 제34권2호
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• pp.139-148
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• 2011

Avian reovirus (ARV) and fowl adenovirus (FAdV) were evaluated for pathogenicity in specific pathogen free (SPF) chickens. ARV was isolated from the broilers with history of malabsorption syndrome (MAS). FAdV was isolated from the layer breeders with inclusion body hepatitis and hydropericardium syndrome. Total 6 inoculated groups including 1 un-inoculated group were organized and inoculated with the ARV and/or FAdV by oral route. The minimal pathological lesions and lower viral gene detection rates were present in the ARV inoculated groups compared to those of FAdV or ARV/FAdV inoculated groups. Common gross lesions in the ARV inoculated group were distended intestine with foamy contents and in the FAdV group there were foamy cecal contents and hydropericardium among the evaluation methods such as gross and histological lesion, viral gene detection, body weight and serum chemistry, histopathological lesion score was reliable especially in the liver lesions such as hepatic necrosis and lymphocytic infiltration. However, we did not success to evaluate the synergetic effect of mixed infection of ARV and FAdV in this study. Therefore, we need further study to reproduce malabsorption syndrome of ARV infection using different viral agent such as rotavirus and using different dose of virus.

• 한국동물위생학회지
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• 제37권3호
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• pp.185-190
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• 2014

We investigated the serological prevalence of avian metapneumovirus (AMPV), avian reovirus (ARV), Mycoplasma gallisepticum (MG) and Mycoplasma synoviae (MS) in 760 broiler breeder (38 flocks), in the Jeonbuk province in 2013. This study was conducted to evaluate the immune and infection status of the broiler breeder flocks against AMPV, ARV, MG, MS by an enzyme-linked immunosorbent assay (ELISA). Serological test for AMPV were positive 37 (97.3%) flocks and 712 (93.6%) broiler breeder and geometric mean antibody titers were $16,350{\pm}10,195$, ARV were high positive rate 100% (38/38) flocks and 97.8% (743/760). The seropositive flocks against MG were 71.1% (27/38) and the geometric mean antibody titers were $2,474{\pm}2,045$, whereas the rates of positive flocks against MS were 50.0% (19/38) and the geometric mean antibody titers were $1,469{\pm}1,230$.

• 한국동물위생학회지
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• 제29권1호
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• pp.9-18
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• 2006

The ELISA titers to avian pneumovirus (APV) and avian reovirus (ARV) were surveyed to sera of 38 breeder farms (78 blocks, 1,560 hens) in Jeonbuk province during February to October, 2005. In APV, the positive ELISA were detected 36 (94.7%) breeders, 71 (91.0%) blocks, 1,057 (67.8%) hens, and their S/P ratio was 1.940. Regionally, the positivity of 24 breeders farms in the Jeonju, Jeongeup, Namwon, and Jangsu were noted as 100%, whereas 85.7% in Iksan. The positivity to species such as Cobb (20), Ross (13) and Hanhyup-3 (5), all of the breeding farms were detected as positive, 40 (86.9%), 17 (94.4%) and 14 (100.0%) in blocks, 553 (60.1%), 285 (79.2%) and 219 (78.2%) in hens, and their mean S/P ratio were 1.677, 1.769 and 2.254, respectively. The positivity of the breeders vaccinated with ARV, all of the 9 breeder farms (38 blocks) were noted as 100%, but 627 (82.5%) in hens, and its mean S/P ratio was 1.273. Whereas nonvaccinated with ARV were 28 (96.5%) in breeders farms, 38 (95.0%) in blocks, 660 (82.5%) in hens, and the mean S/P ratio was 1.612. In species which were vaccinated with ARV, 11 breeder farms (38 blocks) were noted as 100%, but 82.5% in hens, and their mean S/P ratio were 1.315. Whereas in nonvaccinated with ARV, 25 (92.6%) in farms, 38 (95.0%) in blocks and 660 (82.5%) in hens were positive, and their mean S/P ratio was 1.532.

• Molecules and Cells
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• 제26권4호
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• pp.396-403
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• 2008

The first ORF of the ARV S1133 S1 segment encodes the nonstructural protein p10, which is responsible for the induction of cell syncytium formation. However, p10-dependent signaling during syncytium formation is fully unknown. Here, we show that dominant negative RhoA, Rho inhibitor C3 exoenzyme, ROCK/Rho-kinase inhibitor Y-27632 and Rac1 inhibitor NSC23766 inhibit p10-mediated cell fusion. p10 over-expression is concomitant with activation and membrane translocation of RhoA and Rac1, but not cdc42. RhoA and Rac1 downstream events, including JNK phosphorylation and transcription factor AP-1 and $NF-{\kappa}B$ activation, as well as MLC expression and phosphorylation are simultaneously activated by p10. p10 point mutant T13M possessed 20% fusion-inducing ability and four p10 fusion-deficient mutants V15M, V19M, C21S and L32A reduced or lost their ability to activate RhoA and Rac1 signaling. We conclude that p10-mediated syncytium formation proceeds by utilizing RhoA and Rac1-dependent signaling.