Cargando…
Immunization With Outer Membrane Vesicles Derived From Major Outer Membrane Protein-Deficient Salmonella Typhimurium Mutants for Cross Protection Against Salmonella Enteritidis and Avian Pathogenic Escherichia coli O78 Infection in Chickens
Colibacillosis is an economically important infectious disease in poultry, caused by avian pathogenic Escherichia coli (APEC). Salmonella enterica serovar Enteritidis (S. Enteritidis) is a major cause of food-borne diseases in human circulated through poultry-derived products, including meat and chi...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7720508/ https://www.ncbi.nlm.nih.gov/pubmed/33329465 http://dx.doi.org/10.3389/fmicb.2020.588952 |
_version_ | 1783619864482545664 |
---|---|
author | Chen, Yuxuan Jie, Kaiwen Li, Biaoxian Yu, Haiyan Ruan, Huan Wu, Jing Huang, Xiaotian Liu, Qiong |
author_facet | Chen, Yuxuan Jie, Kaiwen Li, Biaoxian Yu, Haiyan Ruan, Huan Wu, Jing Huang, Xiaotian Liu, Qiong |
author_sort | Chen, Yuxuan |
collection | PubMed |
description | Colibacillosis is an economically important infectious disease in poultry, caused by avian pathogenic Escherichia coli (APEC). Salmonella enterica serovar Enteritidis (S. Enteritidis) is a major cause of food-borne diseases in human circulated through poultry-derived products, including meat and chicken eggs. Vaccine control is the mainstream approach for combating these infections, but it is difficult to create a vaccine for the broad-spectrum protection of poultry due to multiple serotypes of these pathogens. Our previous studies have shown that outer membrane vesicles (OMVs) derived from S. enterica serovar Typhimurium mutants with a remodeled outer membrane could induce cross-protection against heteroserotypic Salmonella infection. Therefore, in this study, we further evaluated the potential of broad-spectrum vaccines based on major outer membrane protein (OMP)-deficient OMVs, including ΔompA, ΔompC, and ΔompD, and determined the protection effectiveness of these candidate vaccines in murine and chicken infection models. The results showed that ΔompA led to an increase in the production of OMVs. Notably, ΔompAΔompCΔompD OMVs showed significantly better cross-protection against S. enterica serovar Choleraesuis, S. Enteritidis, APEC O78, and Shigella flexneri 2a than did other omp-deficient OMVs, with the exception of ΔompA OMVs. Subsequently, we verified the results in the chicken model, in which ΔompAΔompCΔompD OMVs elicited significant cross-protection against S. Enteritidis and APEC O78 infections. These findings further confirmed the feasibility of improving the immunogenicity of OMVs by remodeling the outer membrane and provide a new perspective for the development of broad-spectrum vaccines based on OMVs. |
format | Online Article Text |
id | pubmed-7720508 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77205082020-12-15 Immunization With Outer Membrane Vesicles Derived From Major Outer Membrane Protein-Deficient Salmonella Typhimurium Mutants for Cross Protection Against Salmonella Enteritidis and Avian Pathogenic Escherichia coli O78 Infection in Chickens Chen, Yuxuan Jie, Kaiwen Li, Biaoxian Yu, Haiyan Ruan, Huan Wu, Jing Huang, Xiaotian Liu, Qiong Front Microbiol Microbiology Colibacillosis is an economically important infectious disease in poultry, caused by avian pathogenic Escherichia coli (APEC). Salmonella enterica serovar Enteritidis (S. Enteritidis) is a major cause of food-borne diseases in human circulated through poultry-derived products, including meat and chicken eggs. Vaccine control is the mainstream approach for combating these infections, but it is difficult to create a vaccine for the broad-spectrum protection of poultry due to multiple serotypes of these pathogens. Our previous studies have shown that outer membrane vesicles (OMVs) derived from S. enterica serovar Typhimurium mutants with a remodeled outer membrane could induce cross-protection against heteroserotypic Salmonella infection. Therefore, in this study, we further evaluated the potential of broad-spectrum vaccines based on major outer membrane protein (OMP)-deficient OMVs, including ΔompA, ΔompC, and ΔompD, and determined the protection effectiveness of these candidate vaccines in murine and chicken infection models. The results showed that ΔompA led to an increase in the production of OMVs. Notably, ΔompAΔompCΔompD OMVs showed significantly better cross-protection against S. enterica serovar Choleraesuis, S. Enteritidis, APEC O78, and Shigella flexneri 2a than did other omp-deficient OMVs, with the exception of ΔompA OMVs. Subsequently, we verified the results in the chicken model, in which ΔompAΔompCΔompD OMVs elicited significant cross-protection against S. Enteritidis and APEC O78 infections. These findings further confirmed the feasibility of improving the immunogenicity of OMVs by remodeling the outer membrane and provide a new perspective for the development of broad-spectrum vaccines based on OMVs. Frontiers Media S.A. 2020-11-03 /pmc/articles/PMC7720508/ /pubmed/33329465 http://dx.doi.org/10.3389/fmicb.2020.588952 Text en Copyright © 2020 Chen, Jie, Li, Yu, Ruan, Wu, Huang and Liu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Chen, Yuxuan Jie, Kaiwen Li, Biaoxian Yu, Haiyan Ruan, Huan Wu, Jing Huang, Xiaotian Liu, Qiong Immunization With Outer Membrane Vesicles Derived From Major Outer Membrane Protein-Deficient Salmonella Typhimurium Mutants for Cross Protection Against Salmonella Enteritidis and Avian Pathogenic Escherichia coli O78 Infection in Chickens |
title | Immunization With Outer Membrane Vesicles Derived From Major Outer Membrane Protein-Deficient Salmonella Typhimurium Mutants for Cross Protection Against Salmonella Enteritidis and Avian Pathogenic Escherichia coli O78 Infection in Chickens |
title_full | Immunization With Outer Membrane Vesicles Derived From Major Outer Membrane Protein-Deficient Salmonella Typhimurium Mutants for Cross Protection Against Salmonella Enteritidis and Avian Pathogenic Escherichia coli O78 Infection in Chickens |
title_fullStr | Immunization With Outer Membrane Vesicles Derived From Major Outer Membrane Protein-Deficient Salmonella Typhimurium Mutants for Cross Protection Against Salmonella Enteritidis and Avian Pathogenic Escherichia coli O78 Infection in Chickens |
title_full_unstemmed | Immunization With Outer Membrane Vesicles Derived From Major Outer Membrane Protein-Deficient Salmonella Typhimurium Mutants for Cross Protection Against Salmonella Enteritidis and Avian Pathogenic Escherichia coli O78 Infection in Chickens |
title_short | Immunization With Outer Membrane Vesicles Derived From Major Outer Membrane Protein-Deficient Salmonella Typhimurium Mutants for Cross Protection Against Salmonella Enteritidis and Avian Pathogenic Escherichia coli O78 Infection in Chickens |
title_sort | immunization with outer membrane vesicles derived from major outer membrane protein-deficient salmonella typhimurium mutants for cross protection against salmonella enteritidis and avian pathogenic escherichia coli o78 infection in chickens |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7720508/ https://www.ncbi.nlm.nih.gov/pubmed/33329465 http://dx.doi.org/10.3389/fmicb.2020.588952 |
work_keys_str_mv | AT chenyuxuan immunizationwithoutermembranevesiclesderivedfrommajoroutermembraneproteindeficientsalmonellatyphimuriummutantsforcrossprotectionagainstsalmonellaenteritidisandavianpathogenicescherichiacolio78infectioninchickens AT jiekaiwen immunizationwithoutermembranevesiclesderivedfrommajoroutermembraneproteindeficientsalmonellatyphimuriummutantsforcrossprotectionagainstsalmonellaenteritidisandavianpathogenicescherichiacolio78infectioninchickens AT libiaoxian immunizationwithoutermembranevesiclesderivedfrommajoroutermembraneproteindeficientsalmonellatyphimuriummutantsforcrossprotectionagainstsalmonellaenteritidisandavianpathogenicescherichiacolio78infectioninchickens AT yuhaiyan immunizationwithoutermembranevesiclesderivedfrommajoroutermembraneproteindeficientsalmonellatyphimuriummutantsforcrossprotectionagainstsalmonellaenteritidisandavianpathogenicescherichiacolio78infectioninchickens AT ruanhuan immunizationwithoutermembranevesiclesderivedfrommajoroutermembraneproteindeficientsalmonellatyphimuriummutantsforcrossprotectionagainstsalmonellaenteritidisandavianpathogenicescherichiacolio78infectioninchickens AT wujing immunizationwithoutermembranevesiclesderivedfrommajoroutermembraneproteindeficientsalmonellatyphimuriummutantsforcrossprotectionagainstsalmonellaenteritidisandavianpathogenicescherichiacolio78infectioninchickens AT huangxiaotian immunizationwithoutermembranevesiclesderivedfrommajoroutermembraneproteindeficientsalmonellatyphimuriummutantsforcrossprotectionagainstsalmonellaenteritidisandavianpathogenicescherichiacolio78infectioninchickens AT liuqiong immunizationwithoutermembranevesiclesderivedfrommajoroutermembraneproteindeficientsalmonellatyphimuriummutantsforcrossprotectionagainstsalmonellaenteritidisandavianpathogenicescherichiacolio78infectioninchickens |