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中国生物工程杂志

China Biotechnology
China Biotechnology  2016, Vol. 36 Issue (1): 1-6    DOI: 10.13523/j.cb.20160101
    
Expression and Immunological Analysis of Recombinant Tetravalent Envelope Domain III Protein of Dengue Virus
QIU Li-juan1,2, ZHAO Yu-jiao1,2, LI Duo1,2, HUANG Xin-wei1,2, WANG Xiao-dan1,2, XI Jue-min1,2, PAN Yue1,2, CHEN Jun-ying1,2, SUN Qiang-ming1,2
1. Institute of Medical Biology, Chinese Academy of Medical Sciences, and Peking Union Medical College, Kunming 650118, China;
2. Yunnan Key Laboratory of Vaccine Research & Development on Severe Infectious Diseases, Kunming 650118, China
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Abstract  

Four serotypes of dengue virus (DENV1-4) circulate globally, causing more human illness than any other arthropod-borne virus. So far, licensed vaccine against dengue is not yet available. The greatest risk factor for severe dengue is a previous infection with a different DENV serotype. The theory for why sequential heterotypic infections increases risk of severe disease is "antibody- dependent enhancement" (ADE). Previous research determinants that the predominant immune response is against the E protein which is comprised of three structurally distinct domains (DI, DII, DIII). EDIII might exclusively generate potent neutralizing antibodies with little or no cross-reactivity, and therefore of reduced ability to promote ADE. This suggested that EDIII is more likely to be an attractive vaccine. Here, a tetravalent recombinant dengue domain III protein gene sequence were yeast expression optimized and synthesized, then expression plasmids were constructed and transducted into pichia pastoris to selected an high-efficiency expression strain. EDIII protein were obtained by inducing expression and purification followed by identification using SDS-PAGE, Western blot. The result showed that EDIII expression plasmid was successfully constructed and highly expressed in pichia pastoris. Mice immunized with tetravalent DENV DIII generated higher levels of serum titer. In conclusion, a tetravalent recombinant dengue domain III protein with high purity were obtained. It lays a good foundation for the development of dengue vaccine.



Key wordsEnvelope domain III protein      Recombinant protein      Dengue virus      Vaccine     
Received: 24 August 2015      Published: 11 January 2016
ZTFLH:  Q939  
Cite this article:

QIU Li-juan, ZHAO Yu-jiao, LI Duo, HUANG Xin-wei, WANG Xiao-dan, XI Jue-min, PAN Yue, CHEN Jun-ying, SUN Qiang-ming. Expression and Immunological Analysis of Recombinant Tetravalent Envelope Domain III Protein of Dengue Virus. China Biotechnology, 2016, 36(1): 1-6.

URL:

https://manu60.magtech.com.cn/biotech/10.13523/j.cb.20160101     OR     https://manu60.magtech.com.cn/biotech/Y2016/V36/I1/1

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