Evaluation of enzyme immunoassays in the diagnosis of duck plague

dc.contributor.advisorSulochana, S
dc.contributor.authorMalmarugan, S
dc.contributor.authorKAU
dc.date.accessioned2019-03-25T09:04:11Z
dc.date.available2019-03-25T09:04:11Z
dc.date.issued1997
dc.descriptionPGen_US
dc.description.abstractUse of Enzyme immunoassays namely dot ELISA and plate ELISA were evaluated to detect DP viral antibodies in serum samples and in whole blood dried on filter paper strips and their efficacy was compared with standard passive haemagglutination test. Indirect immunoperoxidase test was also used to detect DP viral antigen in paraffin embedded liver and spleen. ASS at 33 per cent level was used for separation of duck globulins and antiduck globulins. The protein concentration of these globulins were 34 mg/ml and 15 mg/ml respectively. The purity of these globulins were tested by IEP and AGPT using antiduck whole serum raised in rabbits. Duck plague hyperimmune serum was raised in healthy ducklings with live attenuated DP vaccine having a virus titre of 3.5 log10 ELD50/0.5 ml. This serum was used as the positive control. A total of 200 serum samples, 35 liver and 30 spleen samples were collected from different localities for the detection of duck plague viral antibodies and antigen. Corresponding blood samples were also collected on filter paper strips and the serum was eluted and ELISA was carried out. The results in this test were then compared with whole serum ELISA. The percentage of positive reaction in PHA, Dot ELISA, plate ELISA and filter paper strip method are 64 per cent, 68 per cent 72.5 per cent and 70.5 per cent respectively. Comparative efficacy of PHA with Dot ELISA, plate ELISA and filter paper strip method were carried out and sensitivity of the tests are 71.87, 67.64 and 77.30 per cent respectively. The specificity of these tests were 38.88, 43.75, 70.90 and 67.79 per cent respectively. The concordance of PHA with these tests were 60, 75.5 and 74.5 per cent respectively. On statistical analysis high degree of association (P<0.05) was observed between PHA and Dot ELISA, plate ELISA and filter paper strip method. Highly significant different (P>0.05) was observed between PHA and plate ELISA, and PHA and filter paper strip method. Based on the results, it was concluded that because of the simplicity, easiness and accuracy, Dot ELISA is suitable for detection of DPV antibodies under field conditions. But plate ELISA was highly sensitive, specific and able to detect low titred sera. Hence this test may be recommended for titration of DPV antibodies in the laboratories, particularly when the potency of the vaccine is to be checked and the immune status of a flock is to be evaluated. Because of various advantages filter paper strip method will serve as an alternative to collection of whole serum for detection of DPV antibodies. For the detection of DPV antigen, IPT was considered as suitable one because of its ability to detect high positive (83%) cases and less non specific reactions.en_US
dc.identifier.citation171249en_US
dc.identifier.urihttp://krishikosh.egranth.ac.in/handle/1/5810099259
dc.keywordsMicrobiology, duck plague, diseases ducken_US
dc.language.isoenen_US
dc.publisherDepartment of Microbiology, College of Veterinary and Animal Sciences, Mannuthyen_US
dc.subMicrobiologyen_US
dc.subjectnullen_US
dc.themeEvaluation study of duck plague diseasesen_US
dc.these.typeM.V.Sc.en_US
dc.titleEvaluation of enzyme immunoassays in the diagnosis of duck plagueen_US
dc.typeThesisen_US
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