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CP and CP-PGN protect mice against MRSA infection by inducing M1 macrophages
Corynebacterium pyruviciproducens (C. pyruviciproducens, CP), as a newly discovered immunomodulator, has been confirmed to have a stronger immunoregulation than Propionibacterium acnes (P. acnes) of the traditional immune adjuvant, by previous experiments with model antigen ovalbumin and sheep red b...
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/PMC5715006/ https://www.ncbi.nlm.nih.gov/pubmed/29203871 http://dx.doi.org/10.1038/s41598-017-17001-0 |
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author | Zhang, Yang Li, Xiang-Xiang Ma, Yuan Xu, Jie Zhao, Li-Na Qian, Xue-Feng Zhang, Xian-Feng Shi, Jin-Fang Han, Qing-Zhen |
author_facet | Zhang, Yang Li, Xiang-Xiang Ma, Yuan Xu, Jie Zhao, Li-Na Qian, Xue-Feng Zhang, Xian-Feng Shi, Jin-Fang Han, Qing-Zhen |
author_sort | Zhang, Yang |
collection | PubMed |
description | Corynebacterium pyruviciproducens (C. pyruviciproducens, CP), as a newly discovered immunomodulator, has been confirmed to have a stronger immunoregulation than Propionibacterium acnes (P. acnes) of the traditional immune adjuvant, by previous experiments with model antigen ovalbumin and sheep red blood cells. Here, it was designed to assess its ability to resist methicillin-resistant Staphylococcus aureus (MRSA), since MRSA as a vital gram positive pathogen is characterized by high morbidity and mortality. In this report, it was indicated that C. pyruviciproducens and its peptidoglycan (CP-PGN) could help to be against bloodstream infection of MRSA with raised survival rate, decreased bacteria load and alleviated systemic inflammation, and these effects of CP-PGN were more pronounced. However, the whole CP was inclined to prevent localized abdominal infection of MRSA from progressing to a systemic infection. And they showed the potential as a therapeutic drug alone or combined with vancomycin. The diversity of capacity of activating macrophages induced by CP and CP-PGN may result in distinct resistance to MRSA in different infection models. Furthermore, both CP and CP-PGN induced M1 macrophages. In conclusion, CP and its PGN could act as promising immune agents to treat and prevent MRSA infection. |
format | Online Article Text |
id | pubmed-5715006 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57150062017-12-08 CP and CP-PGN protect mice against MRSA infection by inducing M1 macrophages Zhang, Yang Li, Xiang-Xiang Ma, Yuan Xu, Jie Zhao, Li-Na Qian, Xue-Feng Zhang, Xian-Feng Shi, Jin-Fang Han, Qing-Zhen Sci Rep Article Corynebacterium pyruviciproducens (C. pyruviciproducens, CP), as a newly discovered immunomodulator, has been confirmed to have a stronger immunoregulation than Propionibacterium acnes (P. acnes) of the traditional immune adjuvant, by previous experiments with model antigen ovalbumin and sheep red blood cells. Here, it was designed to assess its ability to resist methicillin-resistant Staphylococcus aureus (MRSA), since MRSA as a vital gram positive pathogen is characterized by high morbidity and mortality. In this report, it was indicated that C. pyruviciproducens and its peptidoglycan (CP-PGN) could help to be against bloodstream infection of MRSA with raised survival rate, decreased bacteria load and alleviated systemic inflammation, and these effects of CP-PGN were more pronounced. However, the whole CP was inclined to prevent localized abdominal infection of MRSA from progressing to a systemic infection. And they showed the potential as a therapeutic drug alone or combined with vancomycin. The diversity of capacity of activating macrophages induced by CP and CP-PGN may result in distinct resistance to MRSA in different infection models. Furthermore, both CP and CP-PGN induced M1 macrophages. In conclusion, CP and its PGN could act as promising immune agents to treat and prevent MRSA infection. Nature Publishing Group UK 2017-12-04 /pmc/articles/PMC5715006/ /pubmed/29203871 http://dx.doi.org/10.1038/s41598-017-17001-0 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 Zhang, Yang Li, Xiang-Xiang Ma, Yuan Xu, Jie Zhao, Li-Na Qian, Xue-Feng Zhang, Xian-Feng Shi, Jin-Fang Han, Qing-Zhen CP and CP-PGN protect mice against MRSA infection by inducing M1 macrophages |
title | CP and CP-PGN protect mice against MRSA infection by inducing M1 macrophages |
title_full | CP and CP-PGN protect mice against MRSA infection by inducing M1 macrophages |
title_fullStr | CP and CP-PGN protect mice against MRSA infection by inducing M1 macrophages |
title_full_unstemmed | CP and CP-PGN protect mice against MRSA infection by inducing M1 macrophages |
title_short | CP and CP-PGN protect mice against MRSA infection by inducing M1 macrophages |
title_sort | cp and cp-pgn protect mice against mrsa infection by inducing m1 macrophages |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5715006/ https://www.ncbi.nlm.nih.gov/pubmed/29203871 http://dx.doi.org/10.1038/s41598-017-17001-0 |
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