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Expression fusion immunogen by live attenuated Escherichia coli against enterotoxins infection in mice
Previous epidemiological studies have shown that enterotoxins from enterotoxigenic Escherichia coli (ETEC) appear to be the most important causes of neonatal piglet and porcine post‐weaning diarrhoea (PWD). Thus, it is necessary to develop an effective vaccine against ETEC infection. In the present...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6680629/ https://www.ncbi.nlm.nih.gov/pubmed/31210426 http://dx.doi.org/10.1111/1751-7915.13447 |
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author | Feng, Ni Guan, Weikun |
author_facet | Feng, Ni Guan, Weikun |
author_sort | Feng, Ni |
collection | PubMed |
description | Previous epidemiological studies have shown that enterotoxins from enterotoxigenic Escherichia coli (ETEC) appear to be the most important causes of neonatal piglet and porcine post‐weaning diarrhoea (PWD). Thus, it is necessary to develop an effective vaccine against ETEC infection. In the present study, the Kil cassette was inserted into the pseudogene yaiT by homologous recombination to create an attenuated E. coli double selection platform O142(yaiT‐Kil). After that, PRPL‐Kil was replaced with a fusion gene (LTA1‐STa(13)‐STb‐LTA2‐LTB‐STa(13)‐STb) to establish oral vaccines O142(yaiT::LTA1‐STa(13)‐STb‐LTA2‐LTB‐STa(13)‐STb) (ER‐T). Subsequently, BALB/c mice were orally immunized with ER‐T. Results showed that serum IgG and faecal sIgA responded against all ETEC enterotoxins and induced F41 antibody in BALB/c mice by orogastrically inoculation with recombinant E. coli ER‐T. Moreover, the determination of cellular immune response demonstrated that the stimulation index (SI) was significantly higher in immunized mice than in control mice, and a clear trend in the helper T‐cell (Th) response was Th2‐cell (IL‐4) exceed Th1‐cell (IFN‐γ).Our results indicated that recombinant E. coli ER‐T provides effective protection against ETEC infection. |
format | Online Article Text |
id | pubmed-6680629 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66806292019-08-12 Expression fusion immunogen by live attenuated Escherichia coli against enterotoxins infection in mice Feng, Ni Guan, Weikun Microb Biotechnol Research Articles Previous epidemiological studies have shown that enterotoxins from enterotoxigenic Escherichia coli (ETEC) appear to be the most important causes of neonatal piglet and porcine post‐weaning diarrhoea (PWD). Thus, it is necessary to develop an effective vaccine against ETEC infection. In the present study, the Kil cassette was inserted into the pseudogene yaiT by homologous recombination to create an attenuated E. coli double selection platform O142(yaiT‐Kil). After that, PRPL‐Kil was replaced with a fusion gene (LTA1‐STa(13)‐STb‐LTA2‐LTB‐STa(13)‐STb) to establish oral vaccines O142(yaiT::LTA1‐STa(13)‐STb‐LTA2‐LTB‐STa(13)‐STb) (ER‐T). Subsequently, BALB/c mice were orally immunized with ER‐T. Results showed that serum IgG and faecal sIgA responded against all ETEC enterotoxins and induced F41 antibody in BALB/c mice by orogastrically inoculation with recombinant E. coli ER‐T. Moreover, the determination of cellular immune response demonstrated that the stimulation index (SI) was significantly higher in immunized mice than in control mice, and a clear trend in the helper T‐cell (Th) response was Th2‐cell (IL‐4) exceed Th1‐cell (IFN‐γ).Our results indicated that recombinant E. coli ER‐T provides effective protection against ETEC infection. John Wiley and Sons Inc. 2019-06-18 /pmc/articles/PMC6680629/ /pubmed/31210426 http://dx.doi.org/10.1111/1751-7915.13447 Text en © 2019 The Authors. Microbial Biotechnology published by John Wiley & Sons Ltd and Society for Applied Microbiology. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Feng, Ni Guan, Weikun Expression fusion immunogen by live attenuated Escherichia coli against enterotoxins infection in mice |
title | Expression fusion immunogen by live attenuated Escherichia coli against enterotoxins infection in mice |
title_full | Expression fusion immunogen by live attenuated Escherichia coli against enterotoxins infection in mice |
title_fullStr | Expression fusion immunogen by live attenuated Escherichia coli against enterotoxins infection in mice |
title_full_unstemmed | Expression fusion immunogen by live attenuated Escherichia coli against enterotoxins infection in mice |
title_short | Expression fusion immunogen by live attenuated Escherichia coli against enterotoxins infection in mice |
title_sort | expression fusion immunogen by live attenuated escherichia coli against enterotoxins infection in mice |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6680629/ https://www.ncbi.nlm.nih.gov/pubmed/31210426 http://dx.doi.org/10.1111/1751-7915.13447 |
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