Effects of two infectious bursal disease vaccine virus strains on hepatic microsomal enzyme activities in chickens

2006 ◽  
Vol 54 (2) ◽  
pp. 281-293
Author(s):  
Andreja Prevendar Crnić ◽  
D. Sakar ◽  
Jelena Pompe-Gotal ◽  
Z. Biđin ◽  
Ivana Lojkić ◽  
...  
2021 ◽  
Vol 9 (2) ◽  
pp. 80-89
Author(s):  
E. N. OKEKE ◽  
T. TANIMU

An infectious bursal disease virus strain obtained from an pathogenic strain that was attenuated in em-bryonated eggs, is produced in a primary culture of chicken embryo fibroblast, (CEF). This virus has been passaged 10 times further in CEF, and is now intended for use in the active immunisation of chickens against IBD. The vaccinę virus replicates well in CEF giving a titer of up to107.5 TCID50 per ml.  In spite of its pathogenicity for CEF, the vaccine has no pathogenicity for chickens as shown by the absence of gross and histopathological lesions in the bursa of Fabricius (BF) of birds infected with it. Immunogenicity is retained and infact compares favourably with those of other IBD virus strains. The vaccine virus does not revert back to its original pathogenicity but can be adversely affected by storage at room temperature and at 37°C. It could however be stored at +2°C to +8°C or lower for up to six months without loss in potency, The vaccine can be administered by mouth or intramuscularly and as low as 50 TCID50 per bird guarantees full protection. However, as much as 125,000 times the guaranteed dose per bird has been administered without any observable changes in the BF of the affected birds. The field dosage is calculated so that at least one guaranteed dose (i.e. 50 TCID50 ) is still available to each bird even after incubation at 37°C for 7 days. The vaccine did not depress the immune response of chickens to ND vaccine intraocular when administered concurrently with it. The vaccine was tested for safety and immunogenicity in a population of two isolated flocks totalling 8504 birds. The immune status of a flock tested was significantly enhanced as a result of the vaccination (Table 6). More than 10.8 million doses have been issued to the field from 1979 to 1982 and the demand is increasing. Every batch of vaccine produced is tested for viability in CEF, sterility in bacterial culture media and for safety and potency in chickens.


2012 ◽  
Vol 43 (3) ◽  
pp. 1015-1021 ◽  
Author(s):  
Maria Judite Bittencourt Fernandes ◽  
Isabela Cristina Simoni ◽  
Ricardo Harakava ◽  
Eliana Borges Rivas ◽  
Clarice Weis Arns

2014 ◽  
Vol 62 (2) ◽  
pp. 264-273 ◽  
Author(s):  
Ivan Dobrosavljević ◽  
Dejan Vidanović ◽  
Maja Velhner ◽  
Biljana Miljković ◽  
Branislav Lako

Infectious bursal disease virus is an important poultry pathogen. It is distributed worldwide and causes significant economic losses. In this study, a system was adopted for the simultaneous monitoring of vaccine and virulent strains using reverse transcription polymerase chain reaction (RT-PCR). After the decay of maternal antibodies, chickens were vaccinated at the age of 37 days with a virus of intermediate virulence and challenged at 5, 10 and 14 days post vaccination (dpv). The challenge was done with IBDV strain CH/99. Sequencing of the hypervariable region of VP2 has shown that CH/99 belongs to the very virulent group of viruses. The vaccine virus could be found in the bursa of Fabricius, spleen, thymus and bone marrow until 24 dpv. The CH/99 challenge virus was found in the bursa and lymphoid organs when chickens were challenged at 5 and 10 dpv. When challenge was performed at 14 dpv, the pathogenic virus could not be found in the bursa and other lymphoid organs.


1985 ◽  
Vol 54 (3) ◽  
pp. 563-566 ◽  
Author(s):  
Girija Balakrishnan ◽  
M. Ramachandran ◽  
B. D. Banerjee ◽  
Q. Z. Hussain

1. Albino rats were fed on diets containing 30, 120 or 200 g protein/kg with or without the incorporation of dichlorodiphenyltrichloroethane (DDT) or hexachlorocyclohexane (HCH) at 100 mg/kg diet for 4 weeks.2. The activities of the liver microsomal enzymes NADPH-cytochrome reductase (EC 1.6.2.4), flavoprotein- linked monooxygenase (EC 1.14.14.1)and O-demethylase were significantly greater in animals fed on 120 and 200 g protein/kg diet compared with those fed on 30 g protein/kg diet.3. The inclusion of DDT or HCH at all protein intakes led to further significant rises in microsomal enzyme activities but the increases were much greater for animals receiving the 120 and 200 g protein/kg diets than for those receiving the 30 g protein/kg diet.4. The results imply that detoxification of DDT or HCH was carried out more effectively at the higher protein intakes.


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