Evaluation of Pertussis Toxin Expression in B2 and THIJS Media

Whole-cell pertussis vaccine (wP) has been imperative and highly effective in preventing childhood deaths due to pertussis. Pertussis toxin is one of the virulence factors of Bordetella pertussis in all available pertussis vaccines. wP production in Razi Vaccine and Serum Research Institute is accor...

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Main Authors: H. Moradtalab, M. Noofeli, H. Zeighami, F. Haghi
Format: Article
Language:English
Published: Razi Vaccine and Serum Research Institute 2019-03-01
Series:Archives of Razi Institute
Subjects:
Online Access:http://archrazi.areeo.ac.ir/article_117999_860402941e7a8abd236530ed0a28f53c.pdf
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author H. Moradtalab
M. Noofeli
H. Zeighami
F. Haghi
author_facet H. Moradtalab
M. Noofeli
H. Zeighami
F. Haghi
author_sort H. Moradtalab
collection DOAJ
description Whole-cell pertussis vaccine (wP) has been imperative and highly effective in preventing childhood deaths due to pertussis. Pertussis toxin is one of the virulence factors of Bordetella pertussis in all available pertussis vaccines. wP production in Razi Vaccine and Serum Research Institute is according to bioreactor culture of B. pertussis strains in B2 medium. The aim of this study was to evaluate B. pertussis strain 509 PT production in B2 and Thalen-IJssel (THIJS) media by Chinese Hamster Ovary (CHO) cell and enzyme-linked immunosorbent assay methods (ELISA). In the current study, B. pertussis strain 509 was cultured in B2 and THIJS media. Six samples were taken during the log growth phase within 2-3 h intervals (triplicate). The growth rate was calculated using opacity and the quantification of cell-associated and released PT measured by ELISA and CHO cell assays. THIJS medium was significantly showed an increase in the bacterial growth rate. During the first 29 h, bacterial concentrations in B2 and THIJS culture medium were 19 and 29 IOU, respectively. In THIJS medium, greater amount of pertussistoxin production was cell-associated. In B2 medium, maximum cell-associated toxin by ELISA and CHO cell assays were in the ODs of 1.1 and 0.9 and for THIJS medium in the ODs of 1.6 and 1.1, respectively. B. pertussis strain 509 in THIJS medium produced higher cell mass and cell-associated pertussis toxin than that of B2. It can be used for the production of whole-cell vaccine with higher pertussis toxin and accordingly using lower biomass per dose leading to the reduction of vaccine toxicity.
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spelling doaj.art-8f1405b8fd144546a3061ce14f8fb42a2022-12-22T01:22:07ZengRazi Vaccine and Serum Research InstituteArchives of Razi Institute0365-34392008-98722019-03-01741596710.22092/ari.2018.110249.1124117999Evaluation of Pertussis Toxin Expression in B2 and THIJS MediaH. Moradtalab0M. Noofeli1H. Zeighami2F. Haghi3Department of Microbiology and Virology, Faculty of Medical Sciences, Zanjan University of Medical Sciences, Zanjan, IranDepartment of Human Bacterial Vaccines Research and Production, Razi Vaccine and Serum Research Institute, Agricultural Research, Education, and Extension Organization, Karaj, IranDepartment of Microbiology and Virology, Faculty of Medical Sciences, Zanjan University of Medical Sciences, Zanjan, IranDepartment of Microbiology and Virology, Faculty of Medical Sciences, Zanjan University of Medical Sciences, Zanjan, IranWhole-cell pertussis vaccine (wP) has been imperative and highly effective in preventing childhood deaths due to pertussis. Pertussis toxin is one of the virulence factors of Bordetella pertussis in all available pertussis vaccines. wP production in Razi Vaccine and Serum Research Institute is according to bioreactor culture of B. pertussis strains in B2 medium. The aim of this study was to evaluate B. pertussis strain 509 PT production in B2 and Thalen-IJssel (THIJS) media by Chinese Hamster Ovary (CHO) cell and enzyme-linked immunosorbent assay methods (ELISA). In the current study, B. pertussis strain 509 was cultured in B2 and THIJS media. Six samples were taken during the log growth phase within 2-3 h intervals (triplicate). The growth rate was calculated using opacity and the quantification of cell-associated and released PT measured by ELISA and CHO cell assays. THIJS medium was significantly showed an increase in the bacterial growth rate. During the first 29 h, bacterial concentrations in B2 and THIJS culture medium were 19 and 29 IOU, respectively. In THIJS medium, greater amount of pertussistoxin production was cell-associated. In B2 medium, maximum cell-associated toxin by ELISA and CHO cell assays were in the ODs of 1.1 and 0.9 and for THIJS medium in the ODs of 1.6 and 1.1, respectively. B. pertussis strain 509 in THIJS medium produced higher cell mass and cell-associated pertussis toxin than that of B2. It can be used for the production of whole-cell vaccine with higher pertussis toxin and accordingly using lower biomass per dose leading to the reduction of vaccine toxicity.http://archrazi.areeo.ac.ir/article_117999_860402941e7a8abd236530ed0a28f53c.pdfBordetella pertussisPertussis VaccineELISACHO cellsPertussis Toxin
spellingShingle H. Moradtalab
M. Noofeli
H. Zeighami
F. Haghi
Evaluation of Pertussis Toxin Expression in B2 and THIJS Media
Archives of Razi Institute
Bordetella pertussis
Pertussis Vaccine
ELISA
CHO cells
Pertussis Toxin
title Evaluation of Pertussis Toxin Expression in B2 and THIJS Media
title_full Evaluation of Pertussis Toxin Expression in B2 and THIJS Media
title_fullStr Evaluation of Pertussis Toxin Expression in B2 and THIJS Media
title_full_unstemmed Evaluation of Pertussis Toxin Expression in B2 and THIJS Media
title_short Evaluation of Pertussis Toxin Expression in B2 and THIJS Media
title_sort evaluation of pertussis toxin expression in b2 and thijs media
topic Bordetella pertussis
Pertussis Vaccine
ELISA
CHO cells
Pertussis Toxin
url http://archrazi.areeo.ac.ir/article_117999_860402941e7a8abd236530ed0a28f53c.pdf
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