Dynamics of the immune response in laboratory animals to the introduction of a protective protein of the cause of respiratory syncytial infection in cattle

K. V. Kolesnikovich, P. Krasochko
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Abstract

The authors in the article presented the results of assessing the immune response of guinea pigs using the protective protein of the bovine respiratory syncytial infection virus (RSI), obtained using recombinant E. coli BRSV-F1. The research was carried out in the branch laboratory of veterinary biotechnology and infectious animal diseases of the Vitebsk Order of the Badge of Honor of the State Academy of Veterinary Medicine. The average titer of specific antibodies of guinea pigs to the use of the protective protein of the bovine RSI virus was studied in 9 experimental groups and one control group. Blood sampling was carried out at the beginning of the experiment, before the second immunisation and 14 days after the second immunisation. The average titer of specific antibodies to the use of the protective protein of the bovine RSI virus was determined using an indirect hemagglutination reaction with an erythrocyte diagnosticum containing the bovine respiratory syncytial virus (RSV). With the introduction of samples of the prototype vaccine containing the gene encoding the production of the bovine RSI virus protein: group 1 - whole bacteria E. coli BRSV-F1 with an inducer of protein synthesis IPTG; 2nd, whole bacteria E. coli BRSV-F1 with protein synthesis inducer IPTG + 15% adjuvant IZA-15; 3rd, bacterial lysate E. coli BRSV-F1 with an inducer of protein synthesis IPTG; 4th – E. coli bacterial lysate BRSV-F1 with protein synthesis inducer IPTG + 15% adjuvant IZA-15; 5th - protective protein F1 + 15% adjuvant IZA-15; 6th - protective protein F1 + 2% cellulose, 7th - inactivated bovine RSV (JSC «Belvitunipharm») + 15% adjuvant IZA15; 8th - Hiprabovis 4 vaccines (HIPRA, Spain) and 9th - Bovi-shield Gold FP 5 L5 vaccines (Zoetis, USA) - in the experimental groups, an increase in antibody titer in paired blood sera was noted compared to the control group. From the data obtained, it was concluded that the studied samples of the vaccine prototype containing the gene encoding the production of the bovine RSV protein are not inferior in immunogenic activity to the vaccines Bovishield Gold FP 5 L5 and Hiprabovis 4. Therefore, the protective protein of the bovine RSI virus can be included in the composition of vaccines against this pathology to replace the cultural virus.
引入牛呼吸道合胞体感染的保护性蛋白后,实验动物免疫反应的动力学
作者介绍了利用重组大肠杆菌BRSV-F1获得的牛呼吸道合胞感染病毒(RSI)保护蛋白评估豚鼠免疫反应的结果。这项研究是在国家兽医科学院维捷布斯克荣誉勋章兽医生物技术和动物传染病分实验室进行的。采用9个实验组和1个对照组,研究了豚鼠对牛RSI病毒保护蛋白的平均特异性抗体滴度。在实验开始、第二次免疫前和第二次免疫后14天采血。使用含有牛呼吸道合胞病毒(RSV)的红细胞诊断液进行间接血凝反应,确定了使用牛呼吸道合胞病毒保护蛋白的特异性抗体的平均滴度。引入含有编码生产牛RSI病毒蛋白的基因的原型疫苗样品:第1组-全细菌大肠杆菌BRSV-F1用蛋白质诱导剂合成IPTG;2、全菌大肠杆菌BRSV-F1用蛋白质合成诱导剂IPTG + 15%佐剂IZA-15;3、用蛋白质合成诱导剂IPTG裂解大肠杆菌BRSV-F1;4 -大肠杆菌用蛋白质合成诱导剂IPTG + 15%佐剂IZA-15裂解BRSV-F1;5 -保护蛋白F1 + 15%佐剂IZA-15;第6 -保护蛋白F1 + 2%纤维素,第7 -灭活牛RSV (JSC«Belvitunipharm»)+ 15%佐剂IZA15;第8 - Hiprabovis 4疫苗(HIPRA,西班牙)和第9 - Bovi-shield Gold fp5l5疫苗(Zoetis,美国)在实验组中,与对照组相比,配对血清中的抗体滴度有所增加。从所获得的数据可以得出结论,含有编码牛RSV蛋白产生的基因的疫苗原型样品的免疫原性活性不低于Bovishield Gold FP 5 L5和Hiprabovis 4疫苗。因此,可以将牛RSI病毒的保护蛋白纳入抗该病理的疫苗组合物中,以取代培养病毒。
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