Recombinant lactococcus lactis secreting viral protein 1 of enterovirus 71 and its immunogenicity in mice
BIOTECHNOLOGY LETTERS
Authors: Xu, Pengwei; Wang, Yinbiao; Tao, Ling; Wu, Xuan; Wu, Weidong
Abstract
ObjectiveTo construct recombinant Lactococcus lactis (L. lactis) expressing viral protein 1 (VP1) of enterovirus 71 (EV71) and evaluate its immunogenicity to be used as an oral vaccine in BALB/c mice.ResultsRecombinant L. lactis competent in secreting VP1 (similar to 30kDa) into the extracellular environment with the aid of the signal peptide Usp45 was produced. Enzyme-linked immunosorbent assay showed that significant VP1-specific antibody response including the production of both serum IgG and fecal IgA (p<0.05) was elicited in BALB/c mice upon oral immunization with recombinant L. lactis. Moreover, in contrast to negative control, recombinant L. lactis induced adequate neutralizing antibodies in mouse sera (p<0.05) as demonstrated in virus neutralization assay, whereas the presence of neutralizing antibodies in fecal samples was obvious but not significant (p>0.05).ConclusionsRecombinant L. lactis expressing VP1 of EV71 has the potential to be used as an oral vaccine candidate. The findings may provide some preliminary evidences for further development of effective and needle-free EV71 vaccines.
Discovery of Potent EV71 Capsid Inhibitors for Treatment of HFMD
ACS MEDICINAL CHEMISTRY LETTERS
Authors: Li, Peng; Yu, Jun; Hao, Fei; He, Haiying; Shi, Xuyang; Hu, Jiao; Wang, Li; Du, Chunyan; Zhang, Xiao; Sun, Ya; Lin, Fusen; Gu, Zhengxian; Xu, Deming; Chen, Xinsheng; Shen, Liang; Hu, Guoping; Li, Jian; Chen, Shuhui; Xiao, Wei; Wang, Zhenzhong; Guo, Qingming; Chang, Xiujuan; Tian, Xuyang; Lin, Tianwei
Abstract
Enterovirus 71 (EV71) is a major causative agent of hand, foot, and mouth disease (HFMD), which can spread its infections to the central nervous and other systems with severe consequences. The viral caspid protein VP1 is a well-known target for antiviral efficacy because its occupancy by suitable compounds could stabilize the virus capsid, thus preventing uncoating of virus for RNA release. In this Letter, design, synthesis, and biological evaluation of novel anti-EV71 agents (aminopyridyl 1,2,5-thiadiazolidine 1,1-dioxides) are described. One of the most promising compounds (14) showed excellent antiviral activity against EV71 (EC50 = 4 nM) and exhibited excellent in vivo efficacy in the EV71 infected mouse model.