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Published on: February 4, 2018
Purification of periplasmic flagellar antigen from Borrelia microtti
Mehdi Assmar1, Mohammad Soleimani, Farzad Oreiz
1Department of Parasitology, Pasteur Institute of Iran, Tehran.
Abstract:
Borrelia microtti and Borrelia persica are 2 Iranian strains of Borrelia found in western Asia and responsible for relapsing fever. The outer surface antigens of Borrelia undergo variations which are responsible for the relapsing phenomenon. The fixed flagellar antigen is required for diagnosis as the variant antigens cannot be used in serological methods of diagnosis. The fixed flagellar antigen was purified for the first time from the Iranian strain of Borrelia microtti using detergent treatment and shearing in an omnimixer. Periplasmic flagella were extracted, as confirmed by electron microscopy. Sodium dodecyl sulphate-polyacrylamide gel electrophoresis revealed a band corresponding to 42 kDa. Indirect haemagglutination kits were designed using the pure flagella and the complete sonicate of Borrelia and showed 98% sensitivity and 95% specificity.
Insights
Researchers purified a fixed flagellar antigen from Borrelia microtti, an Iranian relapsing fever pathogen. This antigen is crucial for developing accurate diagnostic tools for Borrelia infections.
Area of Science:
- Medical Microbiology
- Parasitology
- Immunology
Background:
- Borrelia microtti and Borrelia persica are Iranian strains causing relapsing fever.
- Variable outer surface antigens hinder reliable serological diagnosis.
- A fixed flagellar antigen is essential for accurate Borrelia diagnosis.
Purpose of the Study:
- To purify the fixed flagellar antigen from the Iranian Borrelia microtti strain.
- To develop and evaluate indirect hemagglutination diagnostic kits using the purified antigen.
Main Methods:
- Purification of fixed flagellar antigen from Borrelia microtti using detergent treatment and shearing.
- Extraction and confirmation of periplasmic flagella via electron microscopy.
- Analysis of antigen purity and molecular weight (42 kDa) using SDS-PAGE.
Main Results:
- Successful isolation and purification of the fixed flagellar antigen from Borrelia microtti.
- Development of indirect hemagglutination kits utilizing purified flagella and Borrelia sonicate.
- Achieved high diagnostic performance: 98% sensitivity and 95% specificity.
Conclusions:
- The purified fixed flagellar antigen from Borrelia microtti is a promising candidate for reliable Borrelia diagnostics.
- The developed indirect hemagglutination kits demonstrate significant potential for accurate detection of relapsing fever.
- This study provides a foundation for improved serological methods against Borrelia infections in endemic regions.
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