Targeting cell membrane adaptation as a novel antimicrobial strategy
Emergence of antibiotic resistance is an example of the incredible plasticity of bacteria to survive in all environments. The search for new antibiotics active against traditional targets is more challenging due not only to the lack of novel natural products to fulfill the current clinical needs aga...
- Autores:
-
Tran, Truc T.
Miller, William R.
Shamoo, Yousif
Arias, César A.
- Tipo de recurso:
- Article of journal
- Fecha de publicación:
- 2016
- Institución:
- Universidad El Bosque
- Repositorio:
- Repositorio U. El Bosque
- Idioma:
- eng
- OAI Identifier:
- oai:repositorio.unbosque.edu.co:20.500.12495/3542
- Acceso en línea:
- http://hdl.handle.net/20.500.12495/3542
https://doi.org/10.1016/j.mib.2016.07.002
https://repositorio.unbosque.edu.co
- Palabra clave:
- Bacitracina
Catelicidinas
Enterococcus faecium
- Rights
- openAccess
- License
- Acceso abierto
| Summary: | Emergence of antibiotic resistance is an example of the incredible plasticity of bacteria to survive in all environments. The search for new antibiotics active against traditional targets is more challenging due not only to the lack of novel natural products to fulfill the current clinical needs against multidrug-resistant (MDR) bacteria, but also for the possible ‘collateral’ effects on the human microbiota. Thus, non-traditional approaches to combat MDR bacteria have been proposed. Here, we discuss the possibility of targeting the membrane response to the antibiotic attack (cell membrane adaptation) as a viable strategy to increase the activity of current antimicrobials, enhance the activity of the innate immune system and prevent development of resistance during therapy using the three-component regulatory system LiaFSR of enterococci as a model. |
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