Use of BHK cell culture-adapted Newcastle disease virus for immunization of chicks

Vaccine ◽  
1992 ◽  
Vol 10 (3) ◽  
pp. 164-166 ◽  
Author(s):  
G.S. Reddy ◽  
V.A. Srinivasan
2010 ◽  
Vol 2010 ◽  
pp. 1-7 ◽  
Author(s):  
Mohd Azmir Arifin ◽  
Maizirwan Mel ◽  
Mohamed Ismail Abdul Karim ◽  
Aini Ideris

The aim of this study is to prepare a model for the production of Newcastle disease virus (NDV) lentogenic F strain using cell culture in bioreactor for live attenuated vaccine preparation. In this study, firstly we investigated the growth of Vero cells in several culture media. The maximum cell number was yielded by culture of Vero cells in Dulbecco's Modified Eagle Medium (DMEM) which was1.93×106 cells/ml. Secondly Vero cells were grown in two-litre stirred tank bioreactor by using several commercial microcarriers. We achieved the maximum cell concentration about7.95×105 cells/ml when using Cytodex 1. Later we produced Newcastle Disease virus in stirred tank bioreactor based on the design developed using Taguchi L4 method. Results reveal that higher multiplicity of infection (MOI) and size of cell inoculums can yield higher virus titer. Finally, virus samples were purified using high-speed centrifugation based on3∗∗(3-1) Fractional Factorial Design. Statistical analysis showed that the maximum virus titer can be achieved at virus sample concentration of 58.45% (v/v), centrifugation speed of 13729 rpm, and centrifugation time of 4 hours. As a conclusion, high yield of virus titer could be achieved through optimization of cell culture in bioreactor and separation by high-speed centrifugation.


2015 ◽  
Vol 46 (3) ◽  
pp. 861-865 ◽  
Author(s):  
Sivam Visnuvinayagam ◽  
Thangavel K ◽  
Lalitha N ◽  
Malmarugan S ◽  
Kuppannan Sukumar

2020 ◽  
Vol 31 (2) ◽  
Author(s):  
Anton Sabri AL-bana

Isolation &identification of Newcastle disease virus from wild pigeonsinhabiting University of Baghdad (Al-Khwarizmi College of engineering)where velogenic and devastating infection of birds was encountered. Chickenembryos fibroblasts (CEF) were used for virus isolation (from infectedspleen and lungs) and propagation. Viral cytopathogenic effect was noticedon infected (CEF) cell culture within (24) hr post inoculation. The virus wasidentified by heamagglutination inhibition (HI) test using reference antiNDV serum.


2007 ◽  
Vol 31 (2) ◽  
pp. 133-140
Author(s):  
Anton Sabri AL-bana

 Isolation &identification of Newcastle disease virus from wild pigeonsinhabiting University of Baghdad (Al-Khwarizmi College of engineering)where velogenic and devastating infection of birds was encountered. Chickenembryos fibroblasts (CEF) were used for virus isolation (from infectedspleen and lungs) and propagation. Viral cytopathogenic effect was noticedon infected (CEF) cell culture within (24) hr post inoculation. The virus wasidentified by heamagglutination inhibition (HI) test using reference antiNDV serum.


1970 ◽  
Vol 7 (2) ◽  
pp. 304-312
Author(s):  
MJ Ara ◽  
MT Islam ◽  
MT Hossain ◽  
MA Haque ◽  
R Ahmed ◽  
...  

The research work was conducted on 105 broiler chicks (Cobb-500) with a view to determine the rate of distribution of Newcastle disease virus (NDV) in various organs following infection through natural (intranasal, intraocular and oral) and parenteral (intravenous, intramuscular and subcutaneous) routes of inoculation at different ages (7, 15 and 28 days of old). Each bird received a dose of 0.2 ml of NVNDV (300 ELD50). Body temperature, onset of clinical signs and mortality of birds (if any) were recorded daily. Blood samples were collected from the birds to determine the serum HI titre before and after infection. Faeces and various tissue samples (brain, lungs, kidney, colon, bursa of Fabricius, spleen and thymus) were collected daily following post-mortem examination of one bird from each sub-group to determine the presence of NDV along with their HA titre through inoculation into embryonated hen eggs. Some representative samples were also inoculated into chicken embryo fibroblast (CEF) cell culture for isolation of NDV. The highest body temperature (³1080F) was recorded in the birds of almost all the experimental groups between 48 and 72 hours of PI. Appearance of clinical sings was observed earlier (between 48 to 72 hours of PI) in parenterally infected birds than those of inoculated through natural routes. The shortest duration (>26-54 hours of PI) and longest duration (67-132 hours of PI) of death time recorded in birds those were inoculated through IV and oral routes of infection respectively. Isolation of NDV was positive from day 2 of PI and onward in all the groups with some minor variations in some cases. The CEF cell culture system was found more sensitive compared to avian embryo. Irrespective of routes of inoculation and age of birds, there was significant (p<0.01) increase in the mean HA titre of NDV with the progression of time. The highest HA titre of NDV was found in the brain tissue followed by lungs and kidney. Significantly (p<0.01) higher HA titre of NDV isolate was recorded in the birds of all the experimental groups inoculated through IV route. Following infection, the MDA titres decreased day by day in the birds with the increase of HA titres of NDV.


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