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Immunization with a novel Clostridium perfringens epsilon toxin mutant rETX(Y196E)-C confers strong protection in mice
Epsilon toxin (ETX) is produced by toxinotypes B and D of Clostridium perfringens. It can induce lethal enterotoxemia in domestic animals, mainly in sheep, goats and cattle, causing serious economic losses to global animal husbandry. In this study, a novel and stable epsilon toxin mutant rETX(Y196E)...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4822168/ https://www.ncbi.nlm.nih.gov/pubmed/27048879 http://dx.doi.org/10.1038/srep24162 |
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author | Yao, Wenwu Kang, Jingjing Kang, Lin Gao, Shan Yang, Hao Ji, Bin Li, Ping Liu, Jing Xin, Wenwen Wang, Jinglin |
author_facet | Yao, Wenwu Kang, Jingjing Kang, Lin Gao, Shan Yang, Hao Ji, Bin Li, Ping Liu, Jing Xin, Wenwen Wang, Jinglin |
author_sort | Yao, Wenwu |
collection | PubMed |
description | Epsilon toxin (ETX) is produced by toxinotypes B and D of Clostridium perfringens. It can induce lethal enterotoxemia in domestic animals, mainly in sheep, goats and cattle, causing serious economic losses to global animal husbandry. In this study, a novel and stable epsilon toxin mutant rETX(Y196E)-C, obtained by substituting the 196th tyrosine (Y196) with glutamic acid (E) and introducing of 23 amino acids long C-terminal peptide, was determined as a promising recombinant vaccine candidate against enterotoxemia. After the third vaccination, the antibody titers against recombinant wild type (rETX) could reach 1:10(5) in each immunized group, and the mice were completely protected from 100 × LD(50) (50% lethal dose) of rETX challenge. The mice in 15 μg subcutaneously immunized group fully survived at the dose of 500 × LD(50) of rETX challenge and 80% of mice survived at 180 μg (1000 × LD(50)) of rETX administration. In vitro, immune sera from 15 μg subcutaneously immunized group could completely protect MDCK cells from 16 × CT(50) (50% lethal dose of cells) of rETX challenge and protect against 10 × LD(50) dose (1.8 μg) of rETX challenge in mice. These data suggest that recombinant protein rETX(Y196E)-C is a potential vaccine candidate for future applied researches. |
format | Online Article Text |
id | pubmed-4822168 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48221682016-04-18 Immunization with a novel Clostridium perfringens epsilon toxin mutant rETX(Y196E)-C confers strong protection in mice Yao, Wenwu Kang, Jingjing Kang, Lin Gao, Shan Yang, Hao Ji, Bin Li, Ping Liu, Jing Xin, Wenwen Wang, Jinglin Sci Rep Article Epsilon toxin (ETX) is produced by toxinotypes B and D of Clostridium perfringens. It can induce lethal enterotoxemia in domestic animals, mainly in sheep, goats and cattle, causing serious economic losses to global animal husbandry. In this study, a novel and stable epsilon toxin mutant rETX(Y196E)-C, obtained by substituting the 196th tyrosine (Y196) with glutamic acid (E) and introducing of 23 amino acids long C-terminal peptide, was determined as a promising recombinant vaccine candidate against enterotoxemia. After the third vaccination, the antibody titers against recombinant wild type (rETX) could reach 1:10(5) in each immunized group, and the mice were completely protected from 100 × LD(50) (50% lethal dose) of rETX challenge. The mice in 15 μg subcutaneously immunized group fully survived at the dose of 500 × LD(50) of rETX challenge and 80% of mice survived at 180 μg (1000 × LD(50)) of rETX administration. In vitro, immune sera from 15 μg subcutaneously immunized group could completely protect MDCK cells from 16 × CT(50) (50% lethal dose of cells) of rETX challenge and protect against 10 × LD(50) dose (1.8 μg) of rETX challenge in mice. These data suggest that recombinant protein rETX(Y196E)-C is a potential vaccine candidate for future applied researches. Nature Publishing Group 2016-04-06 /pmc/articles/PMC4822168/ /pubmed/27048879 http://dx.doi.org/10.1038/srep24162 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Yao, Wenwu Kang, Jingjing Kang, Lin Gao, Shan Yang, Hao Ji, Bin Li, Ping Liu, Jing Xin, Wenwen Wang, Jinglin Immunization with a novel Clostridium perfringens epsilon toxin mutant rETX(Y196E)-C confers strong protection in mice |
title | Immunization with a novel Clostridium perfringens epsilon toxin mutant rETX(Y196E)-C confers strong protection in mice |
title_full | Immunization with a novel Clostridium perfringens epsilon toxin mutant rETX(Y196E)-C confers strong protection in mice |
title_fullStr | Immunization with a novel Clostridium perfringens epsilon toxin mutant rETX(Y196E)-C confers strong protection in mice |
title_full_unstemmed | Immunization with a novel Clostridium perfringens epsilon toxin mutant rETX(Y196E)-C confers strong protection in mice |
title_short | Immunization with a novel Clostridium perfringens epsilon toxin mutant rETX(Y196E)-C confers strong protection in mice |
title_sort | immunization with a novel clostridium perfringens epsilon toxin mutant retx(y196e)-c confers strong protection in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4822168/ https://www.ncbi.nlm.nih.gov/pubmed/27048879 http://dx.doi.org/10.1038/srep24162 |
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