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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Razi Vaccine and Serum Research Institute
2019-03-01
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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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issn | 0365-3439 2008-9872 |
language | English |
last_indexed | 2024-12-11T03:42:06Z |
publishDate | 2019-03-01 |
publisher | Razi Vaccine and Serum Research Institute |
record_format | Article |
series | Archives of Razi Institute |
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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