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Salmonella typhimurium Infection Reduces Schistosoma japonicum Worm Burden in Mice
Coinfection of microorganisms is a common phenomenon in humans and animals. In order to further our understanding of the progress of coinfection and the possible interaction between different pathogens, we have built a coinfection mouse model with Schistosoma japonicum and Salmonella typhimurium, an...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5430953/ https://www.ncbi.nlm.nih.gov/pubmed/28465515 http://dx.doi.org/10.1038/s41598-017-00992-1 |
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author | Zhu, Xiaoyang Chen, Lu Wu, Junfang Tang, Huiru Wang, Yulan |
author_facet | Zhu, Xiaoyang Chen, Lu Wu, Junfang Tang, Huiru Wang, Yulan |
author_sort | Zhu, Xiaoyang |
collection | PubMed |
description | Coinfection of microorganisms is a common phenomenon in humans and animals. In order to further our understanding of the progress of coinfection and the possible interaction between different pathogens, we have built a coinfection mouse model with Schistosoma japonicum and Salmonella typhimurium, and used this model to investigate the systemic metabolic and immune responses using NMR-based metabonomics and immunological techniques. Our results show that Salmonella typhimurium (ATCC14028) infection reduces the number of adult schistosomal worms and eggs, relieves symptoms of schistosomiasis and also abates the mortality of mice infected by Schistosoma japonicum. In addition, Salmonella typhimurium infection counteracts the metabolic disturbances associated with schistosomiasis, which was reflected by the reverted levels of metabolites in coinfected mice, compared with the Schistosoma japonicum infected mice. Furthermore, immune analyses also indicate that shift of the immune response to different pathogens is a result of indirect interactions between Schistosoma japonicum and Salmonella typhimurium within the host. Salmonella typhimurium infection can ameliorate Schistosoma japonicum-caused schistosomiasis in BALB/c mice, which is most likely due to inverse immune polarization. Our work provides an insight into coinfection between Schistosoma japonicum and Salmonella typhimurium, and may further contribute to the development of new tools for controlling Schistosoma japonicum-associated diseases. |
format | Online Article Text |
id | pubmed-5430953 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54309532017-05-16 Salmonella typhimurium Infection Reduces Schistosoma japonicum Worm Burden in Mice Zhu, Xiaoyang Chen, Lu Wu, Junfang Tang, Huiru Wang, Yulan Sci Rep Article Coinfection of microorganisms is a common phenomenon in humans and animals. In order to further our understanding of the progress of coinfection and the possible interaction between different pathogens, we have built a coinfection mouse model with Schistosoma japonicum and Salmonella typhimurium, and used this model to investigate the systemic metabolic and immune responses using NMR-based metabonomics and immunological techniques. Our results show that Salmonella typhimurium (ATCC14028) infection reduces the number of adult schistosomal worms and eggs, relieves symptoms of schistosomiasis and also abates the mortality of mice infected by Schistosoma japonicum. In addition, Salmonella typhimurium infection counteracts the metabolic disturbances associated with schistosomiasis, which was reflected by the reverted levels of metabolites in coinfected mice, compared with the Schistosoma japonicum infected mice. Furthermore, immune analyses also indicate that shift of the immune response to different pathogens is a result of indirect interactions between Schistosoma japonicum and Salmonella typhimurium within the host. Salmonella typhimurium infection can ameliorate Schistosoma japonicum-caused schistosomiasis in BALB/c mice, which is most likely due to inverse immune polarization. Our work provides an insight into coinfection between Schistosoma japonicum and Salmonella typhimurium, and may further contribute to the development of new tools for controlling Schistosoma japonicum-associated diseases. Nature Publishing Group UK 2017-05-02 /pmc/articles/PMC5430953/ /pubmed/28465515 http://dx.doi.org/10.1038/s41598-017-00992-1 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Zhu, Xiaoyang Chen, Lu Wu, Junfang Tang, Huiru Wang, Yulan Salmonella typhimurium Infection Reduces Schistosoma japonicum Worm Burden in Mice |
title | Salmonella typhimurium Infection Reduces Schistosoma japonicum Worm Burden in Mice |
title_full | Salmonella typhimurium Infection Reduces Schistosoma japonicum Worm Burden in Mice |
title_fullStr | Salmonella typhimurium Infection Reduces Schistosoma japonicum Worm Burden in Mice |
title_full_unstemmed | Salmonella typhimurium Infection Reduces Schistosoma japonicum Worm Burden in Mice |
title_short | Salmonella typhimurium Infection Reduces Schistosoma japonicum Worm Burden in Mice |
title_sort | salmonella typhimurium infection reduces schistosoma japonicum worm burden in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5430953/ https://www.ncbi.nlm.nih.gov/pubmed/28465515 http://dx.doi.org/10.1038/s41598-017-00992-1 |
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