Cell-surface display of E7 antigen from human papillomavirus type-16 in Lactococcus lactis and in Lactobacillus plantarum using a new cell-wall anchor from lactobacilli

被引:78
作者
Cortes-Perez, NG
Azevedo, V
Alcocer-González, JM
Rodriguez-Padilla, C
Tamez-Guerra, RS
Corthier, G
Gruss, A
Langella, P
Bermúdez-Humarán, LG
机构
[1] INRA, Unite Rech Laitieres & Genet Appl, F-78352 Jouy En Josas, France
[2] Univ Fed Minas Gerais, ICB, Inst Biol Sci, Belo Horizonte, MG, Brazil
[3] Univ Autonoma Nuevo Leon, Fac Ciencias Biol, Lab Immunol & Virol, San Nicolas De Los 66450, Garza NL, Mexico
[4] INRA, Unite Ecol & Physiol Tube Digestif, F-78352 Jouy En Josas, France
关键词
Lactococcus lactis; Lactobacillus plantarum; E7; antigen; cell-wall anchor;
D O I
10.1080/10611860400024219
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The human papillomavirus type-16 (HPV-16) E7 protein is considered a major viral oncoprotein involved in cervical cancer (CxCa) and a potential candidate for the development of a vaccine against this neoplasia. Here, two lactic acid bacteria (the model one Lactococcus lactis and a probiotic one Lactobacillus plantarum) were engineered to deliver an E7 mutant protein (E7mm), which has a reduced transforming activity and consequently, could fit better to therapeutic use in humans than the native form of E7. An efficient cell-surface display of E7mm was obtained in L. lactis using an expression cassette encoding a precursor composed of (i) the signal peptide and the first 15 amino acids of the mature part of the lactococcal Usp45 protein; (ii) E7mm and (iii) the cell-wall anchor of the Streptococcus pyogenes M6 protein (CWA(M6)). This hybrid precursor was produced but not cell-wall anchored in Lb. plantarum. We thus replaced CWA(M6) by the cell-wall anchor of a Lb. plantarum protein which allows an efficient cell-wall anchoring of E7mm in this bacterium. The E7mm production and cell-surface display in both L. lactis and a probiotic bacterium, Lb. plantarum, represent one more step towards the development of a safe and effective treatment against CxCa.
引用
收藏
页码:89 / 98
页数:10
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