A safe and sensitive enterovirus A71 infection model based on human SCARB2 knock-in mice

被引:26
作者
Zhou, Shuya [1 ]
Liu, Qiang [2 ]
Wu, Xing [3 ]
Chen, Pan [3 ]
Wu, Xi [1 ]
Guo, Yanan [4 ]
Liu, Susu [1 ]
Liang, Zhenglun [3 ]
Fan, Changfa [1 ]
Wang, Youchun [2 ]
机构
[1] Natl Inst Food & Drug Control, Inst Lab Anim Resources, Div Anim Model Res, Beijing 100050, Peoples R China
[2] Natl Inst Food & Drug Control, Minist Hlth Res Qual & Standardizat Biotech Prod, Key Lab, Div HIV AIDS & Sex Transmitted Virus Vaccines, Beijing 100050, Peoples R China
[3] Natl Inst Food & Drug Control, Minist Hlth Res Qual & Standardizat Biotech Prod, Key Lab, Div Hepatitis Vaccine, Beijing 100050, Peoples R China
[4] Biocytogen Co Ltd, Beijing 101111, Peoples R China
基金
中国国家自然科学基金;
关键词
Enterovirus A71 mouse model; hSCARB2; knockin; Bioluminescent imaging; Pseudotype virus; Vaccine effect evaluation; 71; VACCINE; PUBLIC-HEALTH; MOUSE MODEL; CHILDREN; CHINA; COMPLICATIONS; PATHOGENESIS; PROTECTION; PEPTIDES; EFFICACY;
D O I
10.1016/j.vaccine.2016.04.029
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Enterovirus A71 infection has become a severe threat for global public health. Vaccines for controlling and preventing Enterovirus A71 epidemics are highly demanded, however, vaccine evaluation has been hindered by the lack of suitable Enterovirus A71 infection animal models. Here we established an hSCARB2 knockin mouse model for real-time monitoring of enterovirus A71 infection in vivo. This model was sensitive to the infection of both replication-competent virus rEV71(FY)-EGFP and single round pseudo type virus pEV71(FY)-Luc. The intensity of bioluminescence correlated well with viral loads in infected tissues (R=0.86, P<0.01). Pathological changes recapitulated human infectious and clinical features of enterovirus A71, including both general characteristics of "hand foot and mouth" and the severe symptoms in the CNS. A formalin-inactivated enterovirus A71 vaccine can elicit antibodies in R26-hSCARB2 mice, which play effective roles in protecting knockin mice against enterovirus A71 infection as indicated by bioluminescence. Therefore, this work provides a safe, sensitive and visualizing model for exploring mechanisms of enterovirus A71 infection and examining human enterovirus A71 vaccines and antiviral therapies. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2729 / 2736
页数:8
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