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Conformational Evaluation of HIV-1 Trimeric Envelope Glycoproteins Using a Cell-based ELISA Assay
Published on: September 14, 2014
The complex of flavivirus envelope polypeptide with meningococcal proteosomes elicits formation of virus-neutralizing
I Slávik1, P Kuzemenská, O Kozuch
1Institute of Virology, Slovak Academy of Sciences, Bratislava.
Abstract:
Polypeptide E of tick-borne encephalitis virus was isolated in sucrose density gradient and mixed with equal weight portion of meningococcal proteosomes in the presence of N-dodecyl-N,N-dimethylglycine. Mutual complexing of viral and bacterial molecules occurred after removal of detergent by dialysis. Complexed particles appeared in the electron microscope as 40-50 microns thick short-rod structures covered on their surface with both, delicate poppy-like grains, or envelope subunit-like clustered molecules. Even when applied without adjuvant, the complex of tick-borne encephalitis virus polypeptide E with meningococcal proteosomes elicited in mice a marked antiviral as well as antibacterial humoral response.
Insights
This study shows that combining tick-borne encephalitis virus polypeptide E with meningococcal proteosomes creates a complex that generates strong antiviral and antibacterial immune responses in mice, even without adjuvants.
Area of Science:
- Virology
- Immunology
- Microbiology
Background:
- Tick-borne encephalitis virus (TBEV) poses a significant public health threat.
- Developing effective vaccines against TBEV is crucial for disease prevention.
- Meningococcal proteosomes have been explored as potential vaccine adjuvants.
Purpose of the Study:
- To investigate the formation and immunogenicity of a complex between TBEV polypeptide E and meningococcal proteosomes.
- To assess the potential of this complex as a vaccine candidate eliciting both antiviral and antibacterial responses.
Main Methods:
- Isolation of TBEV polypeptide E using sucrose density gradient centrifugation.
- Complex formation between TBEV polypeptide E and meningococcal proteosomes in the presence of N-dodecyl-N,N-dimethylglycine.
- Detergent removal via dialysis to facilitate mutual complexing.
- Characterization of complexed particles using electron microscopy.
- Immunization of mice with the complex and assessment of humoral immune responses.
Main Results:
- Complexed particles were observed as short-rod structures (40-50 microns) with surface features from both viral and bacterial components.
- The TBEV polypeptide E-meningococcal proteosome complex elicited a significant antiviral humoral response in mice.
- The complex also induced a marked antibacterial humoral response against meningococcal components.
Conclusions:
- A novel complex of TBEV polypeptide E and meningococcal proteosomes can be successfully formed.
- This complex demonstrates potent immunogenic properties, inducing both TBEV-specific and meningococcal-specific humoral immunity.
- The findings suggest the potential utility of this complex as a component in a multivalent vaccine formulation.
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