• 제목/요약/키워드: newcastle disease virus

검색결과 119건 처리시간 0.023초

A COMPARISON OF THE V4 STRAIN WITH THE CONVENTIONAL F1 AND M STRAIN OF NEWCASTLE DISEASE VACCINE IN RURAL BANGLADESH

  • Biswas, H.R.;Hoque, M.M.;Chowdhury, S.M.Z.H.;Oxley, M.E.;Rahman, M.M.
    • Asian-Australasian Journal of Animal Sciences
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    • 제9권2호
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    • pp.231-235
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    • 1996
  • Bangladeshi indigenous chickens of mixed ages vaccinated twice at a three week interval with either conventional vaccines-$F_1$ (ocular) and M (mukteswar, Intramuscular), or heat resistant $V_4$ vaccine administered by either the ocular or oral routes, all showed satisfactory hemagglutination inhibition antibody (HI) responses and protection against Newcastle Disease (NCD) challenge persisting for four months. The antibody response to $F_1$ and M was higher than for $V_4$, which was similar whether administered by the ocular or oral routes. All vaccinated treatments have a significant level of protection compare to the control group (p<0.01). No significant difference (p>0.05) in the protection against controlled challenge with virulent NCD virus was found between vaccinated groups.

닭와포자충 감염이 닭의 뉴캣슬병 예방접종에 대한 면역억제 효과 (Immunosuppressive effect of Cryptosporidium baileyi infection on vaccination against Newcastle disease in chicks)

  • 이재구;김현철
    • Parasites, Hosts and Diseases
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    • 제36권2호
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    • pp.121-126
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    • 1998
  • 닭와포자충 감염이 다른 병원체에 대한 닭의 체액성 면역에 미치는 영향을 규명하기 위한 연구의 일환으로 2일령 SPF 병아리에 $5{\;}{\times}10^5$의 닭와포자충 오오시스트를 한 번에 경구투여한 다음 4일과 21일 두 번에 걸척 뉴캣슬병 불활화 (사독) 백신을 접종하였다. 오오시스트 접종 후 2주부터 1주 간격으로 13주까지 채혈하여 혈구응집억제반응으로 ND HI $log_2$ 역가를 경시적으로 측정하여 대조군과 비교, 검토하였다. 일반적으로 뉴캣슬병 바이러스에 대한 Hl가는 전 실험기간을 통하여 대조군에 비하여 실험군이 상당히 낮았으며 (p<0.01), 보다 빨리 음전하는 경향이었다. 백신의 보강주사 후 역가는 점점 높아져서 2주 ($5.00(\;}{\pm}{\;}0$; 비감염 대조군)와 4주 ($3.88{\;}{\pm}{\;}0.6658$; 감염 실험군)에 최고치에 이른 다음 점점 낮아졌다. 한편, 분변 내의 오오시스트 배설 양상은 통상적인 감염례와 같았다. 이로 미루어 보아 병아리가 닭와포자충에 감염되면 건강한 병아리에 비하여 뉴캣슬병 바이러스에 대한 면역억제 현상이 일어나 감수성이 증가할 수 있을 것으로 생각된다.

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Binary Ethylenimine으로 불활화(不活化)한 Newcastle Disease Virus의 항원성(抗原性)과 면역원성(免疫原性)에 관한 연구(硏究) (Studies on the Antigenicity and Immunogenicity of Newcastle Disease Virus Inactivated with Binary Ethylenimine)

  • 박봉균;전윤성;이영순;이영옥
    • 대한수의학회지
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    • 제25권2호
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    • pp.155-165
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    • 1985
  • Effects of binary ethylenimine (BEI) treatment on the inactivation of infectivity and hemagglutinin of Newcastle disease virus (NDV) were studied in comparison with those of formalin treatment. Immune responses of chickens vaccinated with BEI-inactivated NDV vaccines were also investigated. The results were summarized as followings; 1. Complete loss of infectivity of NDV (Bl) was observed at 3, 7, and 24 hours after the treatment at $37^{\circ}C$ with BEI concentrations of 0.01M, 0.005M and 0.001M, respectively. 2. The hemagglutinin activity of NDV (Bl) remained constant when treated with 0.01M BEI at $37^{\circ}C$. However, it gradually decreased when treated with 0.1% or 0.2% formalin at $37^{\circ}C$. 3. When 4-week-old chickens were vaccinated with NDV vaccines prepared from Bl or Miyadera strains of NDV, inactivated with 0.1M BEI and adsorbed to aluminium hydroxide gel, favorable immune responses were observed throughout the 8 weeks of observation period. 4. When these chickens were revaccinated at 8 weeks after the first vaccination, strong anamnestic responses were evoked and the immunity maintained for 4 weeks of the observation. Though slightly bettor immune responses were observed after primary vaccination in chickens vaccinated with Bl vaccine compared with those vaccinated with Miyadera vaccine, the differences were not significant. 5. On the electron microscopy, BEI (0.01M) gave least effect to the envelope as well as capsid of NDV.

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Characterization and Antiviral Effects of Mx Proteins from Various MHC Haplotype Chickens Showing Different Susceptible to Marek's Disease Virus

  • Chang, Kyuug-Soo
    • 대한의생명과학회지
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    • 제16권4호
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    • pp.229-238
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    • 2010
  • Chicken Mx protein (cMx) induced interferon (IFN) is an antiviral protein to inhibit replication of RNA virus, particularly negative stranded RNA virus, through blockage of transfortation of viral RNA and proteins. In order to determine antiviral effects of cMx from different MHC haplotype chicken, we characterized cMx gene by studying on nucleotide sequencing, antiviral effects to Newcastle disease virus, VSV and MDV, and transcription activities. Three types of eMx genes (2,118 bp) were detected from the different MHC haplotype chickens [B19 (N), B15(F) and B21 (GSP)] chickens, which have showed different susceptible to Marek's disease (MD). Several amino acid substitutions were showed in the cMx. The amino acid 548 and 631 in the cMxs from N and F, chickens susceptible to MD, was Val and Asn which was important on antiviral effects, and showed in resistant cMx. Those in the cMx from GSP, chicken resistant to MD, were same that showed in susceptible cMx. Though every cMx transactivated the expression of the reporter gene, the transcription activation by resistant cMx from N and F was lower compared to that by susceptible cMx from GSP. The decease of the cell growth in the resistant cMx cloned cells was seen in comparison with another cMx clone cells. Replication of NDV and VSV was suppressed in the clones with resistant cMx from N and F. NMx258-transducted cells lack of antiviral effects, and NMx437 or NMx646-transducted cells was showed 60% of antiviral effects compared to NMx705. Mean death time (MDT) and hemaggutination (HA) titer to NDV was long and low in the eggs of N and F lines, but short and high in the egg of GSP line. Interestingly, strong suppression to NDV was observed in the clone with N-Mx and in the eggs of N line. However, the effects of Mx for replication of vvMDV1 have not been. Thus, resistant types of cMx, N- and F-Mx, have showed the anti-viral effects to only RNA virus including NDV and VSV, but not to DNA virus. Antiviral effects of cMx were required whole length of amino acid including Val and Asn in amino acid 548 and 631.

IMPROVEMENT AND UTILIZATION OF GENETIC RESOURCES IN NATIVE CHICKEN : RECIPROCAL CROSS BETWEEN TAIWAN COUNTRY CHICKEN AND SINGLE COMB WHITE LEGHORN

  • Lee, Yen-Pai;Huang, Hwei-Huang
    • Asian-Australasian Journal of Animal Sciences
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    • 제2권2호
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    • pp.103-114
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    • 1989
  • Reciprocal crosses were conducted between three strains of Taiwan Country chickens, developed in the National Chung-Hsing University, and two strains of Single Comb White Leghorns, developed in the Taiwan Livestock Research Institute. Traits studied were growing performances, laying performances, egg quality traits and traits concerning disease resistance, including resistance to Marek's disease virus and immune responses to Newcastle disease virus vaccine and to sheep red blood cell. Results indicated that laying performances of Taiwan country chickens were much inferior to White Leghorns, but they matured earlier, their eggs had better shell strength and larger proportion of yolk, and their general disease resistance was much better than White Leghorns. Heterosis were found in laying performances and egg quality traits. The heterosis in laying traits was so large that the hybrid laid as many eggs and as large eggs as did pure strains of White Leghorns. Strategies on the improvement of native chickens and the utilization of genetic merits of native chickens were also discussed.

닭 도축장에서의 뉴캣슬병 바이러스 오염 실태 조사 (Surveillance of Newcastle Disease Virus in Chicken Slaughterhouses)

  • 최강석;이은경;전우진;권준헌;이진화;성환우
    • 한국가금학회지
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    • 제38권2호
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    • pp.97-104
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    • 2011
  • 국내 도축장 및 도축장 출하 닭을 대상으로 NDV 오염 실태를 조사하였다. 조사결과, 닭출하농장, 닭수송용차량, 도축장 현수실, 도축장 냉각수에서 각각 조사 대상건수의 13.0%, 13.3%, 16.0%, 10.8%에서 NDV가 분리되었다. 시기별로 보면 차량, 현수실, 냉각수 모두에서 7월에 가장 많이 바이러스가 분리되었다. Pathotyping RT-PCR을 실시한 결과, 이들 분리된 NDV 분리주는 모두 저병원성 NDV 양성 반응을 나타내었으며, F 단백질 분절 부위에 모두 $^{112}GKQGR/L^{117}$ motif를 가지고 있었다. 본 연구에서 분리된 NDV 분리주의 F 단백질 유전자를 분석하여 보았을 때, 조사한 NDV 분리주 25주 중 24주가 NDV V4주와 같은 유전적 cluster를 형성하였으며, 나머지 1주는 NDV Ulster 2C주와 같은 유전적 cluster를 형성하였다. 이와 같은 연구 결과로 보아 국내에서는 출하 닭, 수송 차량, 현수실, 냉각수 등 생산에서 도축 단계까지 일련의 과정에서 높은 빈도로 저병원성 NDV 오염이 이루어지고 있음을 알 수 있었다.

강병원성 뉴캣슬병 바이러스 한국분리주의 SPF 닭 접종에 따른 병리학적 변화 비교 (Comparative Pathology of chickens Experimentally Inoculated with Virulent Viscerotropic Newcastle Disease Viruses isolated in Korea)

  • I. P. Mo;Y. K. Kwon;M. G. Han;H. W. Seong
    • 한국가금학회지
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    • 제28권2호
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    • pp.99-106
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    • 2001
  • 본 시험의 목적은 국내에서 분리된 강병원성 뉴캣슬병 바이러스를 SPF(specific pathogen free)닭에 접종을 하여 병리학적 변화와 각 조직내의 뉴캣슬병 바이러스 항원의 분포를 조사하여 국내분리 바이러스들간의 조직내 친화성을 비교함으로써 분리 바이러스간 병리학적 차이점을 규명하는 것이다. 병리학적 검사를 위하여 가능한 대부분의 조직을 채취하였으며 항원검사는 특이성을 높이기 위하여 단클론성 항체를 이용하였다. 검사결과를 요약하면 뉴캣슬병 바이러스를 접종한 모든 닭들은 접종 후 3일부터 폐사가 시작되어 접종 후 9일에 100% 폐사하였으며 대부분의 접종군은 접종후 5일에서 6일 사이에 폐사가 있었으나 8248 계군은 접종후 7일에서 9일 사이에 모두 폐사를 하여 다른 접종군과 확연히 다른 폐사양상을 보였다. 그러나, 폐사한 닭들은 접종 바이러스에 관계없이 임상증상은 비슷하였다. 일반적으로 접종 후 3일이 경과하면 급격한 활동저하와 함께 빈사상태를 보였고 일단 빈사상태까지 진행된 접종 닭은 다시 회복하지 못하였다. 병리조직학적 소견은 과거 연구자들이 강병원성 뉴캣슬병에서 흔히 관찰하였던 장, 기낭, 폐장에서의 출혈소견 들을 발견할 수 있었으며 접종한 바이러스에 따른 병리학적 변화의 차이는 뚜렷하지 않았다. 공통적인 병변으로서 대표적인 것은 면역기관인 F. bursa, 흉선, 비장에서의 탐식세포 및 단핵 세포의 괴사로서 과거의 문헌들에서 기술된 병변과 비교해 볼 때 이 면역기관에서의 괴사소견은 강병원성 뉴캣슬병의 가장 특징적인 조직학적 병변인 것으로 판단된다. 조직병변과 바이러스간의 유기적 관계를 알아보기 위해 면역화학조직검사법(Immuno histo chemistry)이 많이 이용되는데 본 실험에서도 이 방법을 사용하여 국내분리주들간의 조직친화성을 비교하여 보았다.지하였으며 폐사율은 각각 1.9%, 1.9%, 2.9%와 1.0%로써 대조군의 4.8%에 비하여 낮은 수준을 보여 질병에 대한 저항능력이 향상되었다.kg/h로 분석되었다. 6. 건조작업 중에 소요되는 전력은 9.5~19.3 Wh/kg이었으며, 연료효율 6.9~9.3kg-$H_2$O/L와 열효율 50.2~65.1%에 의한 수분증발량은 124.0~125.4 kg-$H_2$O/h 로 나타났다. 7. 건조기의 열효율을 70%를 기준으로 평가한다면, 시작기의 열효율은 조금 낮은 수준이며, 열관리 계통의 개선을 필요로 하였다. 8. 제작된 계분건조기의 시작기를 15,000수 규모의 양계농장에서 사용한다면 관행의 계분처리 방법에 비하여 약 590,700(원/월)의 비용을 절감할 수 있을 것으로 추정되었다.

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Comparative Evaluation of Three Purification Methods for the Nucleocapsid Protein of Newcastle Disease Virus from Escherichia coli Homogenates

  • Tan Yan Peng;Ling Tau Chuan;Yusoff Khatijah;Tan Wen Siang;Tey Beng Ti
    • Journal of Microbiology
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    • 제43권3호
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    • pp.295-300
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    • 2005
  • In the present study, the performances of conventional purification methods, packed bed adsorption (PBA), and expanded bed adsorption (EBA) for the purification of the nucleocapsid protein (NP) of Newcastle disease virus (NDV) from Escherichia coli homogenates were evaluated. The conventional methods for the recovery of NP proteins involved multiple steps, such as centrifugation, precipitation, dialysis, and sucrose gradient ultracentrifugation. For the PBA, clarified feedstock was used for column loading, while in EBA, unclarified feedstock was used. Streamline chelating immobilized with $Ni^{2+}$ ion was used as an affinity ligand for both PBA and EBA. The final protein yield obtained in conventional and PBA methods was $1.26\%$ and $5.56\%$, respectively. It was demonstrated that EBA achieved the highest final protein yield of $9.6\%$ with a purification factor of 7. Additionally, the total processing time of the EBA process has been shortened by 8 times compared to that of the conventional method.

Production of Nucleocapsid Protein of Newcastle Disease Virus in Escherichia coli and its Assembly into Ring-and Nucleocapsid-like Particles

  • Kho, Chiew-Ling;Tan, Wen-Siang;Khatijah Yusoff
    • Journal of Microbiology
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    • 제39권4호
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    • pp.293-299
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    • 2001
  • The nucleocapsid(NP) protein of Newcastle disease virus (NDV) and its derivative (NP$\sub$cfus)containing the myc region and six histidine residues fused to its C-terminus were pcpressed aboundantly in Escherichia coli. The proteins were purified by sucrose gradient centrifugation. Both the NP and NP$\sub$cfus/ proteins self-assem- bled into ring-like particles stacked together to from nucleocapsid-like structure which are heterogeneous in length with a diameter of 20${\pm}$2 nm and central holow of 5${\pm}$1 nm. Only a very small amount of the monomers in the particles was linked by inter-molecular disulfide bonds. Fusion of the C-terminal end to 29 amino acids inclusive of the myc epitope and His tag did not impair ring assembly buy inhibited the formation of the long herringbone structures. Immunogold lableing of the particles with the anti-myc antibody showed that the C-terminus of the NP$\sub$cfus/ protein is exposed on the surface of these ring-like particles.

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