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Murine SIGNR1 (CD209b) Contributes to the Clearance of Uropathogenic Escherichia coli During Urinary Tract Infections
Uropathogenic Escherichia coli (UPEC), a Gram-negative bacterial pathogen, is a major causative agent of urinary tract infections (UTIs). However, the molecular mechanisms of how UPEC causes infections have not been determined. Recent studies indicated that certain enteric Gram-negative bacteria int...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6965063/ https://www.ncbi.nlm.nih.gov/pubmed/31998663 http://dx.doi.org/10.3389/fcimb.2019.00457 |
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author | Zhang, Yingmiao Zhang, Song He, Yingxia Sun, Ziyong Cai, Wentong Lv, Yin Jiang, Lingyu Li, Qiao Zhu, Sizhe Li, Wenjin Ye, Chenglin Wu, Bicong Xue, Ying Chen, Hongxiang Cai, Huahua Chen, Tie |
author_facet | Zhang, Yingmiao Zhang, Song He, Yingxia Sun, Ziyong Cai, Wentong Lv, Yin Jiang, Lingyu Li, Qiao Zhu, Sizhe Li, Wenjin Ye, Chenglin Wu, Bicong Xue, Ying Chen, Hongxiang Cai, Huahua Chen, Tie |
author_sort | Zhang, Yingmiao |
collection | PubMed |
description | Uropathogenic Escherichia coli (UPEC), a Gram-negative bacterial pathogen, is a major causative agent of urinary tract infections (UTIs). However, the molecular mechanisms of how UPEC causes infections have not been determined. Recent studies indicated that certain enteric Gram-negative bacteria interact with and hijack innate immune receptors DC-SIGN (CD209a) and SIGNR1 (CD209b), often expressed by antigen-presenting cells (APCs), such as macrophages, leading to dissemination and infection. It was not known whether UPEC could utilize DC-SIGN receptors to promote its infection and dissemination similarly to the enteric pathogens. The results of this study reveal that UPEC interacts with CD209-expressing macrophages and transfectants. This interaction is inhibited by anti-CD209 antibody, indicating that CD209s are receptors for UPEC. Additionally, in contrast to the results of previous studies, mice lacking SIGNR1 are more susceptible to infection of this uropathogen, leading to prolonged bacterial persistence. Overall, the results of our study indicate that the innate immune receptor CD209s participate in the clearance of UPEC during UTIs. |
format | Online Article Text |
id | pubmed-6965063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69650632020-01-29 Murine SIGNR1 (CD209b) Contributes to the Clearance of Uropathogenic Escherichia coli During Urinary Tract Infections Zhang, Yingmiao Zhang, Song He, Yingxia Sun, Ziyong Cai, Wentong Lv, Yin Jiang, Lingyu Li, Qiao Zhu, Sizhe Li, Wenjin Ye, Chenglin Wu, Bicong Xue, Ying Chen, Hongxiang Cai, Huahua Chen, Tie Front Cell Infect Microbiol Cellular and Infection Microbiology Uropathogenic Escherichia coli (UPEC), a Gram-negative bacterial pathogen, is a major causative agent of urinary tract infections (UTIs). However, the molecular mechanisms of how UPEC causes infections have not been determined. Recent studies indicated that certain enteric Gram-negative bacteria interact with and hijack innate immune receptors DC-SIGN (CD209a) and SIGNR1 (CD209b), often expressed by antigen-presenting cells (APCs), such as macrophages, leading to dissemination and infection. It was not known whether UPEC could utilize DC-SIGN receptors to promote its infection and dissemination similarly to the enteric pathogens. The results of this study reveal that UPEC interacts with CD209-expressing macrophages and transfectants. This interaction is inhibited by anti-CD209 antibody, indicating that CD209s are receptors for UPEC. Additionally, in contrast to the results of previous studies, mice lacking SIGNR1 are more susceptible to infection of this uropathogen, leading to prolonged bacterial persistence. Overall, the results of our study indicate that the innate immune receptor CD209s participate in the clearance of UPEC during UTIs. Frontiers Media S.A. 2020-01-10 /pmc/articles/PMC6965063/ /pubmed/31998663 http://dx.doi.org/10.3389/fcimb.2019.00457 Text en Copyright © 2020 Zhang, Zhang, He, Sun, Cai, Lv, Jiang, Li, Zhu, Li, Ye, Wu, Xue, Chen, Cai and Chen. 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 | Cellular and Infection Microbiology Zhang, Yingmiao Zhang, Song He, Yingxia Sun, Ziyong Cai, Wentong Lv, Yin Jiang, Lingyu Li, Qiao Zhu, Sizhe Li, Wenjin Ye, Chenglin Wu, Bicong Xue, Ying Chen, Hongxiang Cai, Huahua Chen, Tie Murine SIGNR1 (CD209b) Contributes to the Clearance of Uropathogenic Escherichia coli During Urinary Tract Infections |
title | Murine SIGNR1 (CD209b) Contributes to the Clearance of Uropathogenic Escherichia coli During Urinary Tract Infections |
title_full | Murine SIGNR1 (CD209b) Contributes to the Clearance of Uropathogenic Escherichia coli During Urinary Tract Infections |
title_fullStr | Murine SIGNR1 (CD209b) Contributes to the Clearance of Uropathogenic Escherichia coli During Urinary Tract Infections |
title_full_unstemmed | Murine SIGNR1 (CD209b) Contributes to the Clearance of Uropathogenic Escherichia coli During Urinary Tract Infections |
title_short | Murine SIGNR1 (CD209b) Contributes to the Clearance of Uropathogenic Escherichia coli During Urinary Tract Infections |
title_sort | murine signr1 (cd209b) contributes to the clearance of uropathogenic escherichia coli during urinary tract infections |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6965063/ https://www.ncbi.nlm.nih.gov/pubmed/31998663 http://dx.doi.org/10.3389/fcimb.2019.00457 |
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