Oral immunization with live Lactococcus lactis expressing rotavirus VP8*subunit induces specific immune response in mice

被引:66
作者
Marelli, Belkis [1 ,2 ]
Rosa Perez, Ana [3 ]
Banchio, Claudia [1 ,2 ]
de Mendoza, Diego [1 ,2 ]
Magni, Christian [1 ,2 ]
机构
[1] Univ Nacl Rosario, Inst Biol Mol & Celular Rosario, IBR, CONICET, RA-2000 Rosario, Santa Fe, Argentina
[2] Univ Nacl Rosario, Fac Ciencias Bioquim & Farmaceut, Dept Microbiol, RA-2000 Rosario, Santa Fe, Argentina
[3] Univ Nacl Rosario, Fac Ciencias Med, Inst Inmunol, RA-2000 Rosario, Santa Fe, Argentina
关键词
Lactococcus lactis; Gene expression; Rotavirus; Vaccine; TOXIN FRAGMENT-C; ACID BACTERIA; NEUTRALIZING ANTIBODIES; FUNCTIONAL-ANALYSIS; RHESUS ROTAVIRUS; BOVINE ROTAVIRUS; MUCOSAL DELIVERY; SUBUNIT PROTEIN; GENE-EXPRESSION; PREGNANT CATTLE;
D O I
10.1016/j.jviromet.2011.04.011
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Rotaviruses are the major cause of worldwide infectious diarrhea in children and vaccination is considered to be the most effective way to control these infections. The development of a mucosal live vaccine using the food-grade lactic acid bacteria Lactococcus lactis as antigen vehicle is an attractive and safe vaccination strategy against rotavirus. In this study, the construction of recombinant L lactis strains able to produce the rotavirus spike-protein subunit VP8* in cytoplasmic. secreted and cell wall-anchored forms is reported. Evaluation of the immune response generated after immunization was conducted in a mouse model. The present study shows that animals inoculated orally with the L lactis strain producing the cytoplasmic form of VP8* (LL1) developed significant levels of intestinal IgA antibodies while animals receiving L lactis producing the cell wall-anchored VP8* form (LL3) exhibited anti-VP8* antibodies at both intestinal and systemic levels. Furthermore, it was observed that intestinal antibodies of the LL1-treated group and serum antibodies of the LL3-treated group were able to block rotavirus infection by 50% and 100%, respectively. These encouraging results represent a step towards the development of a new and safe mucosal vaccine against rotavirus. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:28 / 37
页数:10
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