Title of article :
Comparison of Two Different Methods for the Extraction of Outer Membrane Vesicles from the Bordetella pertussis as a Vaccine Candidate
Author/Authors :
Soltani, M. S Department of Microbiology and Microbial Biotechnology - Faculty of Life Sciences and Biotechnology - Shahid Beheshti University - Tehran, Iran , Eftekhar, F Department of Microbiology and Microbial Biotechnology - Faculty of Life Sciences and Biotechnology - Shahid Beheshti University - Tehran, Iran , Noofeli, M Department of Human Bacterial Vaccines Production and Research - Razi Vaccine and Serum Research Institute - Agricultural Research - Education and Extension Organization (AREEO) - Karaj, Iran , Banihashemi, S. R Department of Immunology - Razi Vaccine and Serum Research Institute - Agricultural Research - Education and Extension Organization (AREEO) - Karaj, Iran , Shahcheraghi, F Department of Bacteriology - Pasteur Institute of Iran - Tehran, Iran
Abstract :
Despite the availability of a vaccine, pertussis is still a worldwide health problem. Outer membrane vesicles
(OMVs) in gram-negative bacteria can stimulate the immune system due to several outer membrane proteins
and are very good candidates in vaccine development. OMVs obtained from Bordetella pertussis contain several
antigens, which are considered immunogenic, and could make them a potential candidate for vaccine
production. The current study aimed to compare the current OMV extraction method (with ultracentrifuge) and
a modified extraction method (without ultracentrifuge) and to evaluate the physicochemical properties as well as
the expression of their main virulence factors. Vaccinal strain BP134 grown on Bordet Gengo agar were
inoculated in Modified Stainer-Scholte medium for mass cultivation. OMVs were prepared using two different
methods. They were then stained and examined with a transmission electron microscope. Protein contents were
measured by the Bradford method, and then the protein profile was evaluated by SDS-PAGE. The presence of
immunogenic antigens was detected by Western blotting. The size and shape of the OMVs obtained from the
modified method without the use of ultracentrifuge were similar to the current method and had a size between
40 and 200 nm. The total protein yields of the OMV isolated using the current and modified methods were 800
and 600 μg/ml, respectively. Evaluating the protein profile of extracted OMVs showed the presence of different
proteins. Finally, the presence of PTX, PRN, and FHA was observed in OMVs extracted from both methods.
Comparison of the two OMV extraction methods showed that the obtained vesicles have a suitable and similar
shape and size as well as the expression of three important pathogenic factors as immunogens. Despite the
relatively low reduction in protein yield as the modified method does not require ultracentrifuge, this extraction
method can be used as a suitable alternative for extracting the outer membrane vesicles from B. pertussis,
especially in developing countries. It should be noted that further experiments including immunogenicity
determination of OMVs obtained as vaccine candidates in animal models are required.
Keywords :
virulence factors , outer membrane vesicle , B. pertussis
Journal title :
Archives of Razi Institute