ON-STATION AND FIELD EVALUATION OF INACTIVATED FOWL CHOLERA VACCINE PRODUCED FROM LOCAL Pasteurella multocida ISOLATES, ETHIOPIA

dc.contributor.advisorDr. Gezahegne Mamo, Dr. Takele Abaynehe
dc.contributor.advisorDr. Esayas Gelaye
dc.contributor.authorZEWDE, TARIKU
dc.date.accessioned2018-10-24T06:33:42Z
dc.date.accessioned2023-11-30T12:54:16Z
dc.date.available2018-10-24T06:33:42Z
dc.date.available2023-11-30T12:54:16Z
dc.date.issued2018-06
dc.descriptionA Thesis submitted to the college of Veterinary Medicine and Agriculture of Addis Ababa University in partial fulfillment of the requirements of the degree of Masters of Veterinary Pasteurella multocida ISOLATES, ETHIOPIA hesis eterinary Science in Veterinary Microbiologyen_US
dc.description.abstractVaccination is one of the common preventive measures of fowl cholera. An experimental study on-station and field evaluation was carried out from November 2017 to April 2018. The objectives of this study were to evaluate the safety, immunogenicity and protective efficacy of inactivated fowl cholera vaccine recently developed at National Veterinary Institute of Ethiopia using local Pasteurella multocida isolate. The vaccine was produced with titer of 2.5x108 cfu/ml and evaluated in 8 weeks old chickens (n=60) by injecting 1 ml through IM (Group I; n=20), 0.5 ml IM route (Group II; n=20) and 20 chickens kept as unvaccinated control. The sera were collected from all groups’ at day 0, 14, 21, 28, and 35 and subjected for antibody titer determination by indirect haemagglutination test. Boostered with the same dose and route after 21 days of primary vaccination. Finally, the vaccinated and control chickens were challenged using virulent strains of Pasteurella multocida at day 15 of post booster vaccination. The study at field level was conducted using 200 chickens isolated in a separate compartment. The chickens were vaccinated with 0.5ml through IM route at day 0 and booster dose was given with 0.5ml after 21 day of primary vaccination. Sera were collected at day 0, 21 and 35 and examined by indirect haemagglutination test. Mean antibody titers of Group I were 1.6±1.2, 211.3±2.1, 244.5±1.2, 319.8±1.2 and 502±1.2 at day 0, 14, 21, 28 and 35, respectively. In Group II, mean antibody titers were 1.3±1.2, 203.7±3.0, 234.2±1.2, 367.2±1.2.5 and 452.9±1.2 at day 0, 14, 21, 28 and 35, respectively. In Group III, mean antibody titer remain constant. In case of protective efficacy, both 1 and 0.5ml dose had 87.5% protection. At field study, the mean antibody titers were 4.2±1.1, 310.4±1.0 and 532.6±1.0 at day 0, 21 and 35, respectively. Formalin killed fowl cholera vaccine induces immune response and mean antibody titer increases after booster vaccination in both control and farm condition. The protective efficacy and immunogenicity between 1 and 0.5 ml dose of the vaccine was found insignificant difference. Therefore, the use of 0.5ml dose with booster vaccination at day 21 after primary vaccination is recommended.en_US
dc.identifier.urihttp://etd.aau.edu.et/handle/123456789/13116
dc.language.isoenen_US
dc.subjectChickensen_US
dc.subjectimmunogenicityen_US
dc.subjectinactivated fowl cholera vaccineen_US
dc.subjectPasteurella multociden_US
dc.titleON-STATION AND FIELD EVALUATION OF INACTIVATED FOWL CHOLERA VACCINE PRODUCED FROM LOCAL Pasteurella multocida ISOLATES, ETHIOPIAen_US
dc.typeThesisen_US

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