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Cell death analysis of recombinant mature epsilon toxin on the kidney cell line
BACKGROUND AND OBJECTIVES: Epsilon toxin is the third hazardous bacterial toxin causing ABS enterotoxaemia in domestic animal. In addition, epsilon toxin is known as a biological warfare agent. The aim of this study was to produce the recombinant mature epsilon toxin to evaluate cell death impact on...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Tehran University of Medical Sciences
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8816699/ https://www.ncbi.nlm.nih.gov/pubmed/35222862 http://dx.doi.org/10.18502/ijm.v13i6.8088 |
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author | Chehreara, Roza Karizi, Shohreh Zare Hosseini, Hamideh Mahmoodzadeh Mirhosseini, Seyed Ali Shafiei, Mohammad Amani, Jafar Kazemi, Rouhollah |
author_facet | Chehreara, Roza Karizi, Shohreh Zare Hosseini, Hamideh Mahmoodzadeh Mirhosseini, Seyed Ali Shafiei, Mohammad Amani, Jafar Kazemi, Rouhollah |
author_sort | Chehreara, Roza |
collection | PubMed |
description | BACKGROUND AND OBJECTIVES: Epsilon toxin is the third hazardous bacterial toxin causing ABS enterotoxaemia in domestic animal. In addition, epsilon toxin is known as a biological warfare agent. The aim of this study was to produce the recombinant mature epsilon toxin to evaluate cell death impact on the kidney cell line. MATERIALS AND METHODS: For this purpose, the sequence of mature epsilon toxin (46–328 aa) in pET28a was cloned and expressed in Escherichia coli BL21 (DE3) and purified by nickel-nitrilotriacetic acid (Ni-NTA) column and confirmed by western blot analysis using HRP conjugated anti-His antibody. Then, to assess the anti-proliferative effects of different concentrations of recombinant epsilon toxin, the MTT assay was done on the HEK293 cell line. The annexin V/PI staining was done to investigate the apoptotic and necrotic cell populations after exposure to epsilon toxin. RESULTS: Induction by 1 mM IPTG for 4 h at 37°C was an optimized condition for expressing mature epsilon toxin in E. coli strain BL21 (DE3). Electrophoresis on SDS-PAGE 12% gel showed the desired band approximately at 38 KDa. Our results showed that recombinant epsilon toxin is mainly expressed as an inclusion body. Furthermore, 100, 150, and 200 μg/mL of mature epsilon toxin are significantly reduced the cell viability (P≤0.05). The considerable increase of necrotic cell percentage was shown after exposing to 100, 150, and 200 μg/mL of mature epsilon toxin (P≤0.05). CONCLUSION: The recombinant mature epsilon toxin had cytotoxic effects and could induce necrosis. |
format | Online Article Text |
id | pubmed-8816699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Tehran University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-88166992022-02-25 Cell death analysis of recombinant mature epsilon toxin on the kidney cell line Chehreara, Roza Karizi, Shohreh Zare Hosseini, Hamideh Mahmoodzadeh Mirhosseini, Seyed Ali Shafiei, Mohammad Amani, Jafar Kazemi, Rouhollah Iran J Microbiol Original Article BACKGROUND AND OBJECTIVES: Epsilon toxin is the third hazardous bacterial toxin causing ABS enterotoxaemia in domestic animal. In addition, epsilon toxin is known as a biological warfare agent. The aim of this study was to produce the recombinant mature epsilon toxin to evaluate cell death impact on the kidney cell line. MATERIALS AND METHODS: For this purpose, the sequence of mature epsilon toxin (46–328 aa) in pET28a was cloned and expressed in Escherichia coli BL21 (DE3) and purified by nickel-nitrilotriacetic acid (Ni-NTA) column and confirmed by western blot analysis using HRP conjugated anti-His antibody. Then, to assess the anti-proliferative effects of different concentrations of recombinant epsilon toxin, the MTT assay was done on the HEK293 cell line. The annexin V/PI staining was done to investigate the apoptotic and necrotic cell populations after exposure to epsilon toxin. RESULTS: Induction by 1 mM IPTG for 4 h at 37°C was an optimized condition for expressing mature epsilon toxin in E. coli strain BL21 (DE3). Electrophoresis on SDS-PAGE 12% gel showed the desired band approximately at 38 KDa. Our results showed that recombinant epsilon toxin is mainly expressed as an inclusion body. Furthermore, 100, 150, and 200 μg/mL of mature epsilon toxin are significantly reduced the cell viability (P≤0.05). The considerable increase of necrotic cell percentage was shown after exposing to 100, 150, and 200 μg/mL of mature epsilon toxin (P≤0.05). CONCLUSION: The recombinant mature epsilon toxin had cytotoxic effects and could induce necrosis. Tehran University of Medical Sciences 2021-12 /pmc/articles/PMC8816699/ /pubmed/35222862 http://dx.doi.org/10.18502/ijm.v13i6.8088 Text en Copyright © 2021 The Authors. Published by Tehran University of Medical Sciences https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International license (https://creativecommons.org/licenses/by-nc/4.0/). Non-commercial uses of the work are permitted, provided the original work is properly cited. |
spellingShingle | Original Article Chehreara, Roza Karizi, Shohreh Zare Hosseini, Hamideh Mahmoodzadeh Mirhosseini, Seyed Ali Shafiei, Mohammad Amani, Jafar Kazemi, Rouhollah Cell death analysis of recombinant mature epsilon toxin on the kidney cell line |
title | Cell death analysis of recombinant mature epsilon toxin on the kidney cell line |
title_full | Cell death analysis of recombinant mature epsilon toxin on the kidney cell line |
title_fullStr | Cell death analysis of recombinant mature epsilon toxin on the kidney cell line |
title_full_unstemmed | Cell death analysis of recombinant mature epsilon toxin on the kidney cell line |
title_short | Cell death analysis of recombinant mature epsilon toxin on the kidney cell line |
title_sort | cell death analysis of recombinant mature epsilon toxin on the kidney cell line |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8816699/ https://www.ncbi.nlm.nih.gov/pubmed/35222862 http://dx.doi.org/10.18502/ijm.v13i6.8088 |
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