• Title/Summary/Keyword: 소 바이러스성 설사병 바이러스

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전문가심층분석 - 소 로타바이러스 설사병 (송아지 바이러스성 설사병)

  • 축산물등급판정소
    • KAPE Magazine
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    • s.174
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    • pp.6-7
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    • 2011
  • 소 로타바이러스 설사병은 송아지 특히 생후 2주 이내의 어린 송아지에 심한 물똥설사를 일으키는 바이러스성 질병으로 전염성이 극히 높은 소의 급성 전염병으로 로타바이러스가 원인체이다. 전 세계적으로 널리 발생되고 있으며 우리나라에서도 바이러스성 송아지 설사병 중에서 가장 문제시 되고 있다.

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Phylogenetic Analysis of Bovine Viral Diarrhea Virus from Nasal Swab Sample of Persistently Infected Cattle in Republic of Korea (한국에서 지속감염우의 콧물로부터 소 바이러스성 설사병 바이러스의 계통발생분석)

  • Song, Moo-Chan;Choi, Kyoung-Seong
    • Journal of Veterinary Clinics
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    • v.26 no.6
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    • pp.582-585
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    • 2009
  • Bovine viral diarrhea virus (BVDV) is an economically important worldwide disease in livestock industry. In this study, the occurrence of BVDV in Korean indigenous cattle was performed by RT-PCR using nasal swab. Twelve of 21 cattle were identified as BVDV positive and classified as persistently infected (PI). These animals showed the occurrence of diseases such as diarrhea and pneumonia. BVDV PI outbreaks were found mostly in PI calves. Sequencing and phylogenetic analysis based on the 5'-untranslated region (UTR) showed that our case belonged to BVDV-2a. These results suggested that the nasal swab sampling was available method for the detection of PI animals, underscoring the need for BVDV control strategies in Korean indigenous cattle.

Outbreak of Bovine Viral Diarrhea Virus in Korean Indigenous Calf (한우송아지에서 소 바이러스성 설사병 바이러스 발생)

  • Song, Moo-Chan;Choi, Kyoung-Seong
    • Journal of Veterinary Clinics
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    • v.26 no.6
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    • pp.578-581
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    • 2009
  • A 25-day-old, Korean indigenous calf was presented with a 10 days history of respiratory disorders and bloody diarrhea, and died. This calf was extremely unthrifty compared to others and had evidence of chronic diarrhea based on matting of feces in the hair of the tail and perineum. Ecchymotic hemorrhages were observed on multiple organs at necropsy. Bovine viral diarrhea virus (BVDV) infection was identified by RT-PCR. The phylogenetic analysis showed that this case belonged to BVDV-2a subgroup and was related to highly pathogenic USA isolate 890 (U18059). This case provided evidence for circulation of BVDV-2 in Republic of Korea. The occurrence of BVDV-2 was also reconfirmed.

Biophysical characteristics of a noncytopathic bovine viral diarrhea virus (세포 비병원성 소 설사병 바이러스의 이화학적 성상 조사)

  • Kweon, Chang-hee;Anthony, Castro E;Woo, Hee-jong
    • Korean Journal of Veterinary Research
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    • v.32 no.1
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    • pp.77-82
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    • 1992
  • A noncytopathic bovine viral diarrhea virus(NC BVDV) strain isolated and purified from persistently infected primary bovine fetal lung(BFL) cells was studied by biophysical methods. The buoyant density of particles of the NC BVDV strain was shown to be between 1,090 and $1,114g/cm^3$ and the maximum virus infectivity occured at $1,098g/cm^3$. Immunoelectron microscopic examination by using the partially purified virus revealed regular spherical particles 30~80nm in diameter. Differences in the genomic size of cytopathic and noncytopathic BVDV from infected cells were not found. A comparison of viral proteins of a noncytopathic and cytopathic strain(NADL) by immunoprecipitation using monoclonal antibody indicated that NC BVDV, compared to cytopathic NADL, was cell associated.

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Coccidiosis in Calves (송아지의 콕시듐병)

  • Ryu, Il-Seon
    • Journal of the korean veterinary medical association
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    • v.43 no.4
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    • pp.315-319
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    • 2007
  • 최근 우리나라 소 사육농가에서 육성 및 자우에서 빈번하게 일어나는 세균성 및 바이러스성 설사병은 익히 알려져 있어 주의 깊게 관찰되어 치료와 예방을 잘하고 있으나, 정작 원충성인 콕시듐 설사병에 대해서는 간과하기 십상이다. 따라서 우리 대동물 임상수의사들도 특히 우상바닥 재료로 왕겨를 사용하는 농가들에 대해 관심깊게 봐두어 짚고 넘어가야 하지 않으면 아니되는 질병인 콕시듐증에 대해 정리하여 소개하고자 한다. 소 콕시듐병은 주로 포유기나 이유직후의 어린 소에서 발생하며, 포자층(Sporozoa)류에 속하는 Coccidia 원충(Potozoa)인 아이메리아(Eimeria) 및 Isospora속의 원충에 기인한 접촉성장염으로 장점막의 상피세포 파괴로 인한 급성출혈성 설사, 빈혈을 주 증상으로 하는 질병이며, 만성으로 될 경우는 성장지연과 생산성의 저하를 나타낸다.

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Simultaneous Detection of Major Pathogens Causing Bovine Diarrhea by Multiplex Real-time PCR Panel (Multiplex real-time PCR을 이용한 송아지 설사병 원인 주요 병원체의 동시검출)

  • Kim, Won-Il;Cho, Yong-Il;Kang, Seog-Jin;Hur, Tai-Young;Jung, Young-Hun;Kim, Nam-Soo
    • Journal of Veterinary Clinics
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    • v.29 no.5
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    • pp.377-383
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    • 2012
  • Bovine diarrhea is a major economical burden to the bovine industry in Korea. Since multiple infectious agents can be involved in bovine diarrhea, differential diagnosis is essential for effective treatment. Therefore, a panel of two multiplex real-time PCR assays which can simultaneously detect six major bovine enteric pathogens [i.e., bovine viral diarrhea virus (BVDV), bovine coronavirus (BCoV), group A bovine rotavirus (BRV), Salmonella spp., Escherichia coli (E. coli) $K99^+$, and Cryptosporidium parvum] was developed and applied to test 97 fecal samples collected from cattle farms in Korea. In addition, microscopic examination was also preformed on the samples to detect Coccidium oocyst. The estimated sensitivity of the multiplex PCR was 0.1 $TCID_{50}$ for BVDV, BCoV and group A BRV, 5 and 0.5 CFU for E. coli $K99^+$ and Salmonella, respectively, and 50 oocysts for Cryptosporidium. The amplification efficiency of the multiplex PCR ranged between 0.97 and 0.99 for each pathogen. Among 97 samples, 36 samples were positive for at least one of the 6 major pathogens and 6 samples were simultaneously positive for 2 pathogens by the multiplex PCR assay. Coccidium oocysts were also detected in 48 samples, which were all collected from over 1 month old calves. In conclusion, the multiplex real-time PCR panel can be a useful tool for fast and accurate diagnosis of calf diarrhea associated with BVDV, BCoV, group A BRV, E. coli $K99^+$, Salmonella, and/or Cryptosporidium and Coccidium may be an important target which needs to be included in the multiplex PCR panel in the future.

Construction of recombinant DNA clone for bovine viral diarrhea virus (소 바이러스성 설사병 바이러스의 유전자 재조합 DNA clone의 작성에 관한 연구)

  • Yeo, Sang-geon;Cho, H.J.;Masri, S.A.
    • Korean Journal of Veterinary Research
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    • v.32 no.3
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    • pp.389-398
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    • 1992
  • Molecular cloning was carried out on the Danish strain of bovine viral diarrhea virus(BVDV) to construct strategy for the diagnostic tools and effective vaccine of BVD afterwards. A recombinant DNA clone(No. 29) was established successfully from cDNA for viral RNA tailed with adenine homopolymer at 3'-end. $^{32}P$-labeled DNA probes of 300~1,800bp fragments, originating from the clone 29, directed specific DNA-RNA hybridization results with BVDV RNA. Recombinant DNA of the clone 29 was about 5,200bp representing 41.6% of the full length of Danish strain's RNA, and restriction sites were recognized for EcoR I, Sst I, Hin d III and Pst I restriction enzymes in the DNA fragment.

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