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Efficient Killing of Multidrug‐Resistant Internalized Bacteria by AIEgens In Vivo
Bacteria infected cells acting as “Trojan horses” not only protect bacteria from antibiotic therapies and immune clearance, but also increase the dissemination of pathogens from the initial sites of infection. Antibiotics are hard and insufficient to treat such hidden internalized bacteria, especial...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8097328/ https://www.ncbi.nlm.nih.gov/pubmed/33977040 http://dx.doi.org/10.1002/advs.202001750 |
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author | Li, Ying Liu, Fei Zhang, Jiangjiang Liu, Xiaoye Xiao, Peihong Bai, Haotian Chen, Shang Wang, Dong Sung, Simon H. P. Kwok, Ryan T. K. Shen, Jianzhong Zhu, Kui Tang, Ben Zhong |
author_facet | Li, Ying Liu, Fei Zhang, Jiangjiang Liu, Xiaoye Xiao, Peihong Bai, Haotian Chen, Shang Wang, Dong Sung, Simon H. P. Kwok, Ryan T. K. Shen, Jianzhong Zhu, Kui Tang, Ben Zhong |
author_sort | Li, Ying |
collection | PubMed |
description | Bacteria infected cells acting as “Trojan horses” not only protect bacteria from antibiotic therapies and immune clearance, but also increase the dissemination of pathogens from the initial sites of infection. Antibiotics are hard and insufficient to treat such hidden internalized bacteria, especially multidrug‐resistant (MDR) bacteria. Herein, aggregation‐induced emission luminogens (AIEgens) such as N,N‐diphenyl‐4‐(7‐(pyridin‐4‐yl) benzo [c] [1,2,5] thiadiazol‐4‐yl) aniline functionalized with 1‐bromoethane (TBP‐1) and (3‐bromopropyl) trimethylammonium bromide (TBP‐2) (TBPs) show potent broad‐spectrum bactericidal activity against both extracellular and internalized Gram‐positive pathogens. TBPs trigger reactive oxygen species (ROS)‐mediated membrane damage to kill bacteria, regardless of light irradiation. TBPs effectively kill bacteria without the development of resistance. Additionally, such AIEgens activate mitochondria dependent autophagy to eliminate internalized bacteria in host cells. Compared to the routinely used vancomycin in clinic, TBPs demonstrate comparable efficacy against methicillin‐resistant Staphylococcus aureus (MRSA) in vivo. The studies suggest that AIEgens are promising new agents for the treatment of MDR bacteria associated infections. |
format | Online Article Text |
id | pubmed-8097328 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80973282021-05-10 Efficient Killing of Multidrug‐Resistant Internalized Bacteria by AIEgens In Vivo Li, Ying Liu, Fei Zhang, Jiangjiang Liu, Xiaoye Xiao, Peihong Bai, Haotian Chen, Shang Wang, Dong Sung, Simon H. P. Kwok, Ryan T. K. Shen, Jianzhong Zhu, Kui Tang, Ben Zhong Adv Sci (Weinh) Full Papers Bacteria infected cells acting as “Trojan horses” not only protect bacteria from antibiotic therapies and immune clearance, but also increase the dissemination of pathogens from the initial sites of infection. Antibiotics are hard and insufficient to treat such hidden internalized bacteria, especially multidrug‐resistant (MDR) bacteria. Herein, aggregation‐induced emission luminogens (AIEgens) such as N,N‐diphenyl‐4‐(7‐(pyridin‐4‐yl) benzo [c] [1,2,5] thiadiazol‐4‐yl) aniline functionalized with 1‐bromoethane (TBP‐1) and (3‐bromopropyl) trimethylammonium bromide (TBP‐2) (TBPs) show potent broad‐spectrum bactericidal activity against both extracellular and internalized Gram‐positive pathogens. TBPs trigger reactive oxygen species (ROS)‐mediated membrane damage to kill bacteria, regardless of light irradiation. TBPs effectively kill bacteria without the development of resistance. Additionally, such AIEgens activate mitochondria dependent autophagy to eliminate internalized bacteria in host cells. Compared to the routinely used vancomycin in clinic, TBPs demonstrate comparable efficacy against methicillin‐resistant Staphylococcus aureus (MRSA) in vivo. The studies suggest that AIEgens are promising new agents for the treatment of MDR bacteria associated infections. John Wiley and Sons Inc. 2021-03-02 /pmc/articles/PMC8097328/ /pubmed/33977040 http://dx.doi.org/10.1002/advs.202001750 Text en © 2021 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers Li, Ying Liu, Fei Zhang, Jiangjiang Liu, Xiaoye Xiao, Peihong Bai, Haotian Chen, Shang Wang, Dong Sung, Simon H. P. Kwok, Ryan T. K. Shen, Jianzhong Zhu, Kui Tang, Ben Zhong Efficient Killing of Multidrug‐Resistant Internalized Bacteria by AIEgens In Vivo |
title | Efficient Killing of Multidrug‐Resistant Internalized Bacteria by AIEgens In Vivo |
title_full | Efficient Killing of Multidrug‐Resistant Internalized Bacteria by AIEgens In Vivo |
title_fullStr | Efficient Killing of Multidrug‐Resistant Internalized Bacteria by AIEgens In Vivo |
title_full_unstemmed | Efficient Killing of Multidrug‐Resistant Internalized Bacteria by AIEgens In Vivo |
title_short | Efficient Killing of Multidrug‐Resistant Internalized Bacteria by AIEgens In Vivo |
title_sort | efficient killing of multidrug‐resistant internalized bacteria by aiegens in vivo |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8097328/ https://www.ncbi.nlm.nih.gov/pubmed/33977040 http://dx.doi.org/10.1002/advs.202001750 |
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