Expression fusion immunogen by live attenuated Escherichia coli against enterotoxins infection in mice
Summary 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...
Main Authors: | , |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2019-09-01
|
Series: | Microbial Biotechnology |
Online Access: | https://doi.org/10.1111/1751-7915.13447 |
id |
doaj-fdfca94df010413396b602f31f4e4e3d |
---|---|
record_format |
Article |
spelling |
doaj-fdfca94df010413396b602f31f4e4e3d2020-11-25T03:30:11ZengWileyMicrobial Biotechnology1751-79152019-09-0112594696110.1111/1751-7915.13447Expression fusion immunogen by live attenuated Escherichia coli against enterotoxins infection in miceNi Feng0Weikun Guan1College of Life Science and Resource Environment Yichun University Yichun ChinaCollege of Life Science and Resource Environment Yichun University Yichun ChinaSummary 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‐STa13‐STb‐LTA2‐LTB‐STa13‐STb) to establish oral vaccines O142(yaiT::LTA1‐STa13‐STb‐LTA2‐LTB‐STa13‐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.https://doi.org/10.1111/1751-7915.13447 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ni Feng Weikun Guan |
spellingShingle |
Ni Feng Weikun Guan Expression fusion immunogen by live attenuated Escherichia coli against enterotoxins infection in mice Microbial Biotechnology |
author_facet |
Ni Feng Weikun Guan |
author_sort |
Ni Feng |
title |
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_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_sort |
expression fusion immunogen by live attenuated escherichia coli against enterotoxins infection in mice |
publisher |
Wiley |
series |
Microbial Biotechnology |
issn |
1751-7915 |
publishDate |
2019-09-01 |
description |
Summary 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‐STa13‐STb‐LTA2‐LTB‐STa13‐STb) to establish oral vaccines O142(yaiT::LTA1‐STa13‐STb‐LTA2‐LTB‐STa13‐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. |
url |
https://doi.org/10.1111/1751-7915.13447 |
work_keys_str_mv |
AT nifeng expressionfusionimmunogenbyliveattenuatedescherichiacoliagainstenterotoxinsinfectioninmice AT weikunguan expressionfusionimmunogenbyliveattenuatedescherichiacoliagainstenterotoxinsinfectioninmice |
_version_ |
1724577009399496704 |