Saxena Anjani, Kumar Rajesh, Saxena Mumtesh Kumar
Department of Veterinary Biochemistry and Physiology, College of Veterinary and Animal Sciences, G.B. Pant University of Agriculture and Technology, Pantnagar, Uttarakhand, India.
Department of Veterinary Microbiology, College of Veterinary and Animal Sciences, G.B. Pant University of Agriculture and Technology, Pantnagar, Uttarakhand, India.
Vet World. 2017 Aug;10(8):946-949. doi: 10.14202/vetworld.2017.946-949. Epub 2017 Aug 19.
Typhoid is one of the most important food and water borne disease causing millions of deaths over the world. Presently, there is no cost effective vaccine available in India. The outer-membrane proteins (Omps) of have been exhibited as a potential candidate for development of subunit vaccine against typhoid. The objective of the present study was to evaluate the use of recombinant Omp 28 protein for immunization of rabbit to elucidate its protection against virulent Typhi.
Immune potential of recombinant Omp28 was tested in New Zealand Rabbits. Rabbits were divided into two groups, i.e., control and test group. Control group was injected with phosphate buffer saline with adjuvant while test group were injected with recombinant Omp28 along with adjuvant. Rabbits were bleed and serum was collected from each rabbit. Serum was tested by Enzyme-linked immunosorbent assay (ELISA) for humoral response. Rabbits were challenged with virulent culture to test the protective immunity.
Humoral response was provoked at 15 day and maintained till 30 day. The mean ELISA titer at 15 day was 1 : 28000 (mean titer log 10 : 4.4472) and on the 30 day was 1 : 25866 (mean titer log 10 : 4.4127). Protective immune potential of Omp 28 was assessed by challenge studies in rabbits for which vaccinated and control rabbits were challenged with 10 cells of virulent culture of . Typhi. In control group, out of six, no rabbit could survive after 48 days while in vaccinated group, three out of six rabbit were survived.
Immunization of rabbit with recombinant Omp 28 induced a strong humoral response which was exhibited by high antibody titer in ELISA. Subsequently, intraperitoneal homologous challenge of the immunized New Zealand rabbit resulted in lack of significant protection. These findings indicate that Omp 28 though provoked the humoral immunity but could not provide the protective immunity in rabbit model.
伤寒是最重要的食源性和水源性疾病之一,在全球导致数百万人死亡。目前,印度没有性价比高的疫苗。伤寒杆菌的外膜蛋白(Omps)已被证明是开发伤寒亚单位疫苗的潜在候选物。本研究的目的是评估重组Omp 28蛋白用于兔免疫以阐明其对伤寒杆菌强毒株的保护作用。
在新西兰兔中测试重组Omp28的免疫潜力。将兔分为两组,即对照组和试验组。对照组注射含佐剂的磷酸盐缓冲盐水,而试验组注射重组Omp28和佐剂。对兔进行采血并从每只兔收集血清。通过酶联免疫吸附测定(ELISA)检测血清的体液反应。用强毒培养物对兔进行攻毒以测试保护性免疫。
在第15天激发了体液反应并维持到第30天。第15天的平均ELISA滴度为1:28000(平均滴度log10:4.4472),第30天为1:25866(平均滴度log10:4.4127)。通过在兔中进行攻毒研究评估Omp 28的保护性免疫潜力,为此用伤寒杆菌强毒培养物的10个菌细胞对接种疫苗的兔和对照兔进行攻毒。在对照组中,6只兔中有0只在48天后存活,而在接种疫苗组中,6只兔中有3只存活。
用重组Omp 28对兔进行免疫诱导了强烈的体液反应,这在ELISA中表现为高抗体滴度。随后,对免疫的新西兰兔进行腹腔内同源攻毒导致缺乏显著保护作用。这些发现表明,Omp 28虽然激发了体液免疫,但在兔模型中不能提供保护性免疫。