Standardization Of Avian Leukosis Diagnostic Techniques Through Polymerase Chain Reaction (Pcr) And Confirmation With Enzyme Linked Immunosorbant Assay (Elisa)
By: Abdul Razzaq (M.Phil)
| Prof. Dr. Zafar Iqbal Ch.
Contributor(s): Mr. Asim Aslam | Prof. Dr.Abdul Rauf Shakoori | Faculty of Veterinary Sciences.
Material type: 
BookPublisher: 2006Subject(s): Department of PathologyDDC classification: 0943,T Dissertation note: Avian Leukosis Virus type J infection of chickens is a neoplastic disease affecting chickens. ALV-J is of great economic significance not only because of tumor mortality, but also because of decreased egg production in meat breeding stocks, increased rate of infections, poor response to vaccination and weight suppression in broilers. There is wide spread prevalence of ALV-A and ALV-J in commercial chicken flocks. For control of ALV's eradication programmes based solely on dam testing may be less effective than those where dam testing is combined with procedures to mitigate early horizontal transmission in progeny chicks. For this purpose PCR along with antigen capture ELISA was used in combination for detection of ALV-J proviral DNA, and ALV group specific antigen i.e. p 27 antigen of ALV-J. Polymerase chain reaction technique was standardized by using improved version of H7 primers specific for ALV sub group J targeting env gene encoding gp85 for the detection of avian leucosis virus type J and its confirmation was carried out by comparing it with antigen capture immunosorbant assay which measures group-specific antigen (GSA) i.e. p27 antigen. Feather pulp and serum samples from 50 broiler birds of up to 7 weeks of age were randomly selected from 10 different broiler poultry farms of district Lahore Pakistan. The prevalence of ALV-J was 22 % for antigen capture immunosorbant ELISA and 34 % for polymerase chain reaction (PCR).
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Thesis
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UVAS Library Thesis Section | Veterinary Science | 0943,T (Browse shelf) | Available | 0943,T |
Avian Leukosis Virus type J infection of chickens is a neoplastic disease affecting chickens. ALV-J is of great economic significance not only because of tumor mortality, but also because of decreased egg production in meat breeding stocks, increased rate of infections, poor response to vaccination and weight suppression in broilers. There is wide spread prevalence of ALV-A and ALV-J in commercial chicken flocks. For control of ALV's eradication programmes based solely on dam testing may be less effective than those where dam testing is combined with procedures to mitigate early horizontal transmission in progeny chicks. For this purpose PCR along with antigen capture ELISA was used in combination for detection of ALV-J proviral DNA, and ALV group specific antigen i.e. p 27 antigen of ALV-J. Polymerase chain reaction technique was standardized by using improved version of H7 primers specific for ALV sub group J targeting env gene encoding gp85 for the detection of avian leucosis virus type J and its confirmation was carried out by comparing it with antigen capture immunosorbant assay which measures group-specific antigen (GSA) i.e. p27 antigen. Feather pulp and serum samples from 50 broiler birds of up to 7 weeks of age were randomly selected from 10 different broiler poultry farms of district Lahore Pakistan. The prevalence of ALV-J was 22 % for antigen capture immunosorbant ELISA and 34 % for polymerase chain reaction (PCR).
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