Autor: |
Chu YY; Interfaculty Institute of Microbiology and Infectious Diseases Tübingen (IMIT), Microbial Genetics, University of Tübingen, Tübingen, Germany., Nega M, Wölfle M, Plener L, Grond S, Jung K, Götz F |
Jazyk: |
angličtina |
Zdroj: |
PLoS pathogens [PLoS Pathog] 2013; Vol. 9 (9), pp. e1003654. Date of Electronic Publication: 2013 Sep 26. |
DOI: |
10.1371/journal.ppat.1003654 |
Abstrakt: |
The knowledge that many pathogens rely on cell-to-cell communication mechanisms known as quorum sensing, opens a new disease control strategy: quorum quenching. Here we report on one of the rare examples where Gram-positive bacteria, the 'Staphylococcus intermedius group' of zoonotic pathogens, excrete two compounds in millimolar concentrations that suppress the quorum sensing signaling and inhibit the growth of a broad spectrum of Gram-negative beta- and gamma-proteobacteria. These compounds were isolated from Staphylococcus delphini. They represent a new class of quorum quenchers with the chemical formula N-[2-(1H-indol-3-yl)ethyl]-urea and N-(2-phenethyl)-urea, which we named yayurea A and B, respectively. In vitro studies with the N-acyl homoserine lactone (AHL) responding receptor LuxN of V. harveyi indicated that both compounds caused opposite effects on phosphorylation to those caused by AHL. This explains the quorum quenching activity. Staphylococcal strains producing yayurea A and B clearly benefit from an increased competitiveness in a mixed community. |
Databáze: |
MEDLINE |
Externí odkaz: |
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