Protective immune responses of recombinant VP2 subunit antigen of infectious bursal disease virus in chickens

被引:29
作者
Pradhan, Satya Narayan [1 ]
Prince, Prabhu Rajaiah [1 ]
Madhumathi, Jayaprakasam [1 ]
Roy, Parimal [2 ]
Narayanan, Rangarajan Badri [1 ]
Antony, Usha [1 ]
机构
[1] Anna Univ, Ctr Biotechnol, Madras 600025, Tamil Nadu, India
[2] Tamil Nadu Vet & Anim Sci Univ, Ctr Anim Hlth Studies, Madras 600051, Tamil Nadu, India
关键词
Chicken; IBDV; VP2; Epitope; Immune response; Subunit vaccine; B-CELL EPITOPES; NEWCASTLE-DISEASE; IBDV VP2; VACCINE; STRAINS; IMMUNOSUPPRESSION; IMMUNIZATION; EXPRESSION; SEQUENCE; PROTEIN;
D O I
10.1016/j.vetimm.2012.06.019
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Infectious bursal disease virus (IBDV) is the causative agent of Gumboro disease and poses a huge threat to poultry industry. The risks associated with conventional attenuated viral vaccines make it indispensable to probe into the development of novel and rationally designed subunit vaccines which are safer as well as effective. VP2 is the major host-protective antigen found in IBDV capsid. It encompasses different independent epitopes responsible for the induction of neutralizing antibody. Here, we report the efficacy of the immunodominant fragment of VP2 which induces both humoral and cellular immunity against infectious bursal disease. A 366 bp fragment (52-417 bp) of the VP2 gene from an IBDV field isolate was amplified and expressed in Escherichia coli as a 21 kDa recombinant protein. The efficacy of rVP2(52-417) antigen was compared with two commercial IBDV whole virus vaccine strains. The rVP2(52-417) induced significantly high antibody titres in chicken compared to commercial vaccines and the anti-rVP2(52-417) sera showed reactivity with viral antigens from both commercial strains (P < 0.0001) and field isolates. Also, the chicken splenocytes from rVP2(52-417) immunized group showed a significantly high proliferation (P < 0.01) compared to other groups, which implies that the rVP2(52-417) fragment contains immunogenic epitopes capable of eliciting both B and T cell responses. Further, rvP2(52-417) conferred 100% protection against vIBDV challenge in the immunized chickens which was significantly higher (P < 0.001) compared to 55-60% protection by commercial vaccine strains. Hence, the study confirms the efficacy of the immunodominant VP2 fragment that could be used as a potent vaccine against IBDV infection in chicken. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:293 / 301
页数:9
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