Production of human papillomavirus type 16 L1 virus-like particles by recombinant Lactobacillus casei cells

被引:60
|
作者
Aires, KA
Cianciarullo, AM
Carneiro, SM
Villa, LL
Boccardo, E
Pérez-Martinez, G
Perez-Arellano, I
Oliveira, MLS [1 ]
Ho, PL
机构
[1] Inst Butantan, Ctr Biotecnol, Sao Paulo, Brazil
[2] Inst Butantan, Genet Lab, Sao Paulo, Brazil
[3] Inst Butantan, Lab Biol Celular, Sao Paulo, Brazil
[4] Univ Sao Paulo, Inst Ciencias Biomed, Interuni Biotecnol, BR-05508 Sao Paulo, Brazil
[5] Inst Ludwig Pesquisa Sobre O Canc, Sao Paulo, Brazil
[6] CSIC, Inst Agroquim & Tecnol Alimentos, E-46010 Valencia, Spain
[7] Inst Invest Citological Caja Ahorros Valencia, Valencia, Spain
[8] Univ Sao Paulo, Inst Quim, Sao Paulo, Brazil
[9] Univ Sao Paulo, Inst Biociencias, Sao Paulo, Brazil
关键词
D O I
10.1128/AEM.72.1.745-752.2006
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Infections with human papillomavirus type 16 (HPV-16) are closely associated with the development of human cervical carcinoma, which is one of the most common causes of cancer death in women worldwide. At present, the most promising vaccine against HPV-16 infection is based on the L1 major capsid protein, which self-assembles in virus-like particles (VLPs). In this work, we used a lactose-inducible system based on the Lactobacillus casei lactose operon promoter (plac) for expression of the HPV-16 L1 protein in L. casei. Expression was confirmed by Western blotting, and an electron microscopy analysis of L. casei expressing L1 showed that the protein was able to self-assemble into VLPs intracellularly. The presence of conformational epitopes on the L. casei-produced VLPs was confirmed by immunofluorescence using the anti-HPV-16 VLP conformational antibody H16.V5. Moreover, sera from mice that were subcutaneously immunized with L. casei expressing L1 reacted with Spodoptera frugiperda-produced HPV-16 L1 VLPs, as determined by an enzyme-linked immunosorbent assay. The production of L1 VLPs by Lactobacillus opens the possibility for development of new live mucosal prophylactic vaccines.
引用
收藏
页码:745 / 752
页数:8
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