Sammanfattning
The continuing emergence and spread of antibiotic-resistant bacteria is worrisome and new strategies to curb bacterial infections are being sought. The interference of bacterial quorum sensing (QS) signaling has been suggested as a prospective antivirulence strategy. The AI-2 QS system is present in multiple bacterial species and has been shown to be correlated with pathogenicity. To facilitate the discovery of novel compounds interfering with AI-2 QS, we established a high-throughput setup of whole-cell bioreporter assay, which can be performed in either 96- or 384-well format. Agonistic or antagonistic activities of the test compounds against Escherichia coli LsrB-type AI-2 QS system are monitored by measuring the level of beta-galactosidase expression. A control strain expressing beta-galactosidase in quorum sensing-independent manner is included into the assay for false-positive detection.
Originalspråk | engelska |
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Tidskrift | Journal of Microbiological Methods |
Volym | 154 |
Sidor (från-till) | 40-45 |
Antal sidor | 6 |
ISSN | 0167-7012 |
DOI | |
Status | Publicerad - nov. 2018 |
MoE-publikationstyp | A1 Tidskriftsartikel-refererad |
Vetenskapsgrenar
- 1182 Biokemi, cell- och molekylärbiologi
- 1183 Växtbiologi, mikrobiologi, virologi
- 317 Farmaci