A Pro-Drug Approach for Selective Modulation of AI-2-Mediated Bacterial Cell-to-Cell Communication
Autor: | Shizuka Nakayama, Jacqueline A. I. Smith, Min Guo, Sonja Gamby, Herman O. Sintim |
---|---|
Jazyk: | angličtina |
Rok vydání: | 2012 |
Předmět: |
Salmonella typhimurium
Cell signaling quorum sensing inhibitor enteric bacteria Cell Communication medicine.disease_cause lcsh:Chemical technology Biochemistry Article Bacterial cell structure Analytical Chemistry Lactones ester pro-drug Bacterial Proteins autoinducer processing Escherichia coli Homoserine medicine DPD analog Prodrugs lcsh:TP1-1185 Electrical and Electronic Engineering Receptor Instrumentation lsr expression biology AI-2 Quorum Sensing Prodrug biology.organism_classification Atomic and Molecular Physics and Optics autoinducer cell permeation Quorum sensing Autoinducer Bacteria |
Zdroj: | Sensors Volume 12 Issue 3 Pages 3762-3772 Sensors, Vol 12, Iss 3, Pp 3762-3772 (2012) Sensors (Basel, Switzerland) |
ISSN: | 1424-8220 |
DOI: | 10.3390/s120303762 |
Popis: | The universal quorum sensing autoinducer, AI-2, is utilized by several bacteria. Analogs of AI-2 have the potential to modulate bacterial behavior. Selectively quenching the communication of a few bacteria, in the presence of several others in an ecosystem, using analogs of AI-2 is non-trivial due to the ubiquity of AI-2 processing receptors in many bacteria that co-exist. Herein, we demonstrate that when an AI-2 analog, isobutyl DPD (which has been previously shown to be a quorum sensing, QS, quencher in both Escherichia coli and Salmonella typhimurium) is modified with ester groups, which get hydrolyzed once inside the bacterial cells, only QS in E. coli, but not in S. typhimurium, is inhibited. The origin of this differential QS inhibition could be due to differences in analog permeation of the bacterial membranes or ester hydrolysis rates. Such differences could be utilized to selectively target QS in specific bacteria amongst a consortium of other species that also use AI-2 signaling. |
Databáze: | OpenAIRE |
Externí odkaz: |