AIMS Microbiology, 2017, 3(2): 248-266. doi: 10.3934/microbiol.2017.2.248.

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Evaluation of antibody response against recombinant domain III proteins of dengue virus type 1 and 2

Bioprocess Scale up Facility, Defence Research and Development Establishment, Jhansi Road, Gwalior-474002, India

Dengue, a mosquito borne viral disease caused by dengue virus has emerged as a major health problem during the last few decades. The envelope domain III (DIII) protein of dengue virus is highly immunogenic and capable of inducing neutralizing antibodies against wild-type dengue virus. The envelope domain III protein is a potential subunit vaccine candidate as well as a diagnostic reagent for dengue. This report describes the high yield production and immunogenicity of recombinant DIII proteins of dengue virus type 1 and 2. The subunit DIII proteins were produced in Escherichia coli using batch and fed-batch fermentation process. Immobilized metal affinity chromatography was used to capture DIII proteins of dengue virus type 1 and 2. The purified proteins were refolded by diafiltration to achieve biologically active proteins. After fed-batch fermentation, the recombinant E. coli resulted in purified DIII proteins of about 10.06 mg and 47.70 mg per gram of dry cell weight for recombinant dengue virus type 1 and 2 respectively with more than 95% purity. Biological function of the purified DIII proteins were confirmed by their ability to generate DIII specific antibodies in mice. The DIII antigens in combination with adjuvant resulted antibody endpoint titers of 1:64,000 and 1:1,28,000 for recombinant dengue virus type 1 and 2 respectively. These findings establish that the DIII proteins in combination with adjuvant are immunogenic, which suggests that refolded and purified DIII proteins can be a potential vaccine candidates.
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Keywords fermentation; scale up; purification; vaccine; ELISA; immunogenicity

Citation: Nagesh K Tripathi, Ambuj Shrivastava. Evaluation of antibody response against recombinant domain III proteins of dengue virus type 1 and 2. AIMS Microbiology, 2017, 3(2): 248-266. doi: 10.3934/microbiol.2017.2.248


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This article has been cited by

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  • 2. Nagesh K. Tripathi, Divyanshi Karothia, Ambuj Shrivastava, Swati Banger, Jyoti S. Kumar, Enhanced production and immunological characterization of recombinant West Nile virus envelope domain III protein, New Biotechnology, 2018, 46, 7, 10.1016/j.nbt.2018.05.002
  • 3. Nagesh K. Tripathi, Ambuj Shrivastava, Recent Developments in Recombinant Protein–Based Dengue Vaccines, Frontiers in Immunology, 2018, 9, 10.3389/fimmu.2018.01919

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