Birds and Rabbit Medicine Department, Faculty of Veterinary Medicine, University of Sadat City, Sadat City, Minoufiya, 22857, Egypt.
Middle East for Vaccine Company (MEVAC™), Second Industrial Area, El-Salhyia El-Gededa, Sharkia, 44671, Egypt; Virology Department, Faculty of Veterinary Medicine, University of Sadat City Sadat City, Minoufiya, 22857, Egypt.
Comp Immunol Microbiol Infect Dis. 2021 Feb;74:101601. doi: 10.1016/j.cimid.2020.101601. Epub 2020 Nov 25.
In this study, two highly pathogenic avian influenza (HPAI) H5N8 viruses were isolated from chicken and geese in 2018 and 2019 (Chicken/ME-2018 and Geese/Egypt/MG4/2019). The hemagglutinin and neuraminidase gene analyses revealed their close relatedness to the clade-2.3.4.4b H5N8 viruses isolated from Egypt and Eurasian countries. A monovalent inactivated oil-emulsion vaccine containing a reassortant virus with HA gene of the Chicken/ME-2018/H5N8 strain and a bivalent vaccine containing same reassortant virus plus a previously generated reassortant H5N1 strain (CK/Eg/RG-173CAL/17). The safety of both vaccines was evaluated in specific-pathogen-free (SPF) chickens. To evaluate the efficacy of the prepared vaccines, 2-week-old SPF chickens were vaccinated with 0.5 mL of a vaccine formula containing 10/EID /dose from each strain via the subcutaneous route. Vaccinated birds were challenged with either wild-type HPAI-H5N8 or H5N1 viruses separately at 3 weeks post-vaccine. Results revealed that both vaccines induced protective hemagglutination-inhibiting (HI) antibody titers as early as 2 weeks PV (≥5.0 log). Vaccinated birds were protected clinically against both subtypes (100 % protection). HPAI-H5N1 virus shedding was significantly reduced in birds that were vaccinated with the bivalent vaccine; meanwhile, HPAI-H5N8 virus shedding was completely neutralized in both tracheal and cloacal swabs after 3 days post-infection in birds that had been vaccinated with either vaccine. In conclusion, the developed bivalent vaccine proved to be efficient in protecting chickens clinically and reduced virus shedding via the respiratory and digestive tracts. The applicability of the multivalent avian influenza vaccines further supported their value to facilitate vaccination programs in endemic countries.
在这项研究中,从 2018 年和 2019 年的鸡和鹅中分离出了两株高致病性禽流感(HPAI)H5N8 病毒(鸡/ME-2018 和鹅/埃及/MG4/2019)。血凝素和神经氨酸酶基因分析表明,它们与从埃及和欧亚国家分离出的 2.3.4.4b 分支的 H5N8 病毒密切相关。含有 HA 基因来自鸡/ME-2018/H5N8 株的单价灭活油乳剂疫苗和含有相同重配病毒加先前产生的重配 H5N1 株(CK/Eg/RG-173CAL/17)的双价疫苗。两种疫苗的安全性在无特定病原体(SPF)鸡中进行了评估。为了评估制备疫苗的效果,将 2 周龄 SPF 鸡通过皮下途径用含有 10/EID /剂量的每种疫苗的 0.5 mL 疫苗配方进行接种。接种后 3 周,通过单独用野生型 HPAI-H5N8 或 H5N1 病毒攻毒来评估接种鸡的效果。结果表明,两种疫苗均可在 2 周 PV 时(≥5.0 对数)诱导保护性血凝抑制(HI)抗体滴度。接种鸡对两种亚型均有 100%的保护(临床保护)。接种双价疫苗的鸡的 HPAI-H5N1 病毒滴度显著降低;同时,接种两种疫苗的鸡在感染后 3 天,气管和泄殖腔拭子中的 HPAI-H5N8 病毒滴度完全中和。总之,开发的双价疫苗在临床上对鸡有效,并通过呼吸道和消化道减少了病毒的排出。多价禽流感疫苗的适用性进一步支持了其在流行地区促进疫苗接种计划的价值。