Protection of Khaki Campbell Ducks against Duck Plague Using an Inactivated Duck Plague Vaccine

Q4 Veterinary World''s Veterinary Journal Pub Date : 2023-06-25 DOI:10.54203/scil.2023.wvj36
T. Ahamed, Papia Sultana, Md. Zaminur Rahman, Palash Bose, M. Rafiqul Islam, M. Khatun, Md. Ariful Islam
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Abstract

Duck plague (DP) or duck viral enteritis is a fatal viral disease of ducks that causes huge economic losses in the duck industry. The present study was performed to determine the immune response and protective efficacy of an inactivated DP vaccine prepared from a local virulent DP virus. A virulent DP virus was obtained from the laboratory repository of the Department of Microbiology and Hygiene, Bangladesh Agricultural University, Mymensingh (Bangladesh). The DP virus (EID50 105.3/ml) was inactivated using 0.04% formalin. The alum (40 g/L) was added to the inactivated DP virus as an adjuvant. A total of 60 Khaki Campbell male ducks aged 17 weeks were randomly divided into three groups. Ducks of groups A (n = 20) and B (n = 20) were vaccinated intramuscularly in the breast muscle with 1 ml of inactivated DP vaccine and a live attenuated DP vaccine, respectively. Ducks of group C (n = 20) were kept as unvaccinated control. Booster vaccination was administered at 2 weeks after primary vaccination. Antibody titers of vaccinated ducks were measured at 7, 14, 21, and 28 days post-vaccination (DPV) using a passive haemagglutination (PHA) test. Ducks of both vaccinated and unvaccinated groups were challenged with 1 ml virulent DP virus (EID50 104.3/ml) at 28 DPV. Clinical signs, morbidity and mortality, and gross pathological lesions of vaccinated and control ducks were observed for 10 days post-challenge to evaluate the protective efficacy of inactivated DP vaccine. The mean PHA antibody titers of vaccinated ducks of group A at 7, 14, 21, and 28 DPV were 5 ± 0.43, 26 ± 1.71, 43 ± 3.4, and 54 ± 3.28, respectively. Ducks in group B had mean serum PHA antibody titers of 21 ± 1.71, 41 ± 3.28, 52 ± 3.41, and 84 ± 7.25 at 7, 14, 21, and 28 DPV, respectively. No mortality or gross pathological lesions were observed in vaccinated ducks after they were subjected to a challenge infection. Additionally, no significant difference was observed between groups A and B in terms of the challenge infection. The mortality rate of the control group of ducks was 70%. Hemorrhage in the trachea and intestine and necrotic foci in the liver were seen in unvaccinated control ducks (group C). Experimentally developed inactivated DP vaccine induced a protective serum antibody titer and conferred 100% protection against virulent challenge infection up to 10 days observation period.
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用灭活鸭瘟疫苗保护卡其坎贝尔鸭免受鸭瘟
鸭瘟(DP)或鸭病毒性肠炎是一种致命的鸭子病毒性疾病,给养鸭业造成巨大的经济损失。本研究旨在确定由当地DP毒力病毒制备的DP灭活疫苗的免疫应答和保护效果。从Mymensingh(孟加拉国)孟加拉国农业大学微生物学和卫生系的实验室库中获得了一种致命性DP病毒。0.04%福尔马林灭活DP病毒(EID50 105.3/ml)。将明矾(40 g/L)加入灭活的DP病毒中作为佐剂。选取17周龄卡其坎贝尔公鸭60只,随机分为3组。A组(n = 20)和B组(n = 20)分别在胸肌肌内接种1 ml DP灭活疫苗和1 ml DP减毒活疫苗。C组(n = 20)作为未接种疫苗的对照组。初次接种后2周进行加强接种。采用被动血凝(PHA)试验,分别在接种后7、14、21和28天检测接种鸭的抗体滴度。接种疫苗组和未接种疫苗组的鸭在28 DPV时均被1 ml毒力DP病毒(EID50 104.3/ml)攻毒。在攻毒后10 d观察接种鸭和对照鸭的临床症状、发病率和死亡率以及大体病理病变,以评价DP灭活疫苗的保护效果。A组接种疫苗鸭在7、14、21和28 DPV时的平均PHA抗体滴度分别为5±0.43、26±1.71、43±3.4和54±3.28。B组鸭在7、14、21和28 DPV时的平均血清PHA抗体滴度分别为21±1.71、41±3.28、52±3.41和84±7.25。未观察到接种疫苗的鸭在遭受攻毒感染后死亡或大体病理病变。此外,在攻毒感染方面,A组和B组之间没有显著差异。对照组鸭的死亡率为70%。未接种疫苗的对照鸭(C组)出现了气管和肠道出血以及肝脏坏死灶。实验开发的DP灭活疫苗可诱导保护性血清抗体滴度,并在10天的观察期内对毒攻感染提供100%的保护。
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来源期刊
World''s Veterinary Journal
World''s Veterinary Journal Veterinary-Veterinary (all)
CiteScore
1.00
自引率
0.00%
发文量
43
期刊介绍: The World''s Veterinary Journal (ISSN 2322-4568) is an international, peer reviewed open access journal aims to publish the high quality material from veterinary scientists'' studies. All accepted articles are published Quarterly in full text on the Internet. WVJ publishes the results of original scientific researches, reviews, case reports and short communications, in all fields of veterinary science. In details, topics are: Behavior Environment and welfare Animal reproduction and production Parasitology Endocrinology Microbiology Immunology Pathology Pharmacology Epidemiology Molecular biology Immunogenetics Surgery Virology Physiology Vaccination Gynecology Exotic animals Animal diseases Radiology Ophthalmology Dermatology Chronic disease Anatomy Non-surgical pathology issues of small to large animals Cardiology and oncology.
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