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...

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Main Authors: Ni Feng, Weikun Guan
Format: Article
Language:English
Published: Wiley 2019-09-01
Series:Microbial Biotechnology
Online Access:https://doi.org/10.1111/1751-7915.13447
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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
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