It appears you don't have support to open PDFs in this web browser. To view this file, Open with your PDF reader
Abstract
Enterococcus faecalis is a natural inhabitant of the human gastrointestinal tract. This bacterial species is subdominant in a healthy physiological state of the gut microbiota (eubiosis) in adults, but can become dominant and cause infections when the intestinal homeostasis is disrupted (dysbiosis). The relatively high concentrations of bile acids deoxycholate (DCA) and taurocholate (TCA) hallmark eubiosis and dysbiosis, respectively. This study aimed to better understand how E. faecalis adapts to DCA and TCA. We showed that DCA impairs E. faecalis growth and possibly imposes a continuous adjustment in the expression of many essential genes, including a majority of ribosomal proteins. This may account for slow growth and low levels of E. faecalis in the gut. In contrast, TCA had no detectable growth effect. The evolving transcriptome upon TCA adaptation showed the early activation of an oligopeptide permease system (opp2) followed by the adjustment of amino acid and nucleotide metabolisms. We provide evidence that TCA favors the exploitation of oligopeptide resources to fuel amino acid needs in limiting oligopeptide conditions. Altogether, our data suggest that the combined effects of decreased DCA and increased TCA concentrations can contribute to the rise of E. faecalis population during dysbiosis.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details
1 Université Paris-Saclay, INRAE, AgroParisTech, Micalis Institute, Jouy-en-Josas, France (GRID:grid.462293.8) (ISNI:0000 0004 0522 0627)
2 Université Paris-Saclay, INRAE, AgroParisTech, Micalis Institute, Jouy-en-Josas, France (GRID:grid.462293.8) (ISNI:0000 0004 0522 0627); Université de Strasbourg, INRAE, SVQV UMR-A 1131, Colmar, France (GRID:grid.507621.7)
3 Université Paris-Saclay, INRAE, MaIAGE, Jouy-en-Josas, France (GRID:grid.503376.4)
4 Université Paris-Saclay, INRAE, AgroParisTech, Micalis Institute, Jouy-en-Josas, France (GRID:grid.462293.8) (ISNI:0000 0004 0522 0627); ImmunoSearch, Les Cyclades, Chemin de Camperousse, Grasse, France (GRID:grid.462293.8)
5 Universidade Federal de Minas Gerais, ICB/UFMG, Minas Gerais, Belo Horizonte, Brazil (GRID:grid.8430.f) (ISNI:0000 0001 2181 4888)
6 Université Paris-Saclay, INRAE, AgroParisTech, Micalis Institute, Jouy-en-Josas, France (GRID:grid.462293.8) (ISNI:0000 0004 0522 0627); Universidade Federal de Minas Gerais, ICB/UFMG, Minas Gerais, Belo Horizonte, Brazil (GRID:grid.8430.f) (ISNI:0000 0001 2181 4888)
7 USR3756 CNRS, Institut Pasteur, Department of Computational Biology, Paris, France (GRID:grid.428999.7) (ISNI:0000 0001 2353 6535)
8 Université Paris-Saclay, INRAE, MGP, Jouy-en-Josas, France (GRID:grid.507621.7)
9 Inserm, Centre de Recherche Saint-Antoine, CRSA, AP-HP, Hôpital Saint Antoine, Sorbonne Université, Paris, France (GRID:grid.412370.3) (ISNI:0000 0004 1937 1100)
10 Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC), Gif-sur-Yvette, France (GRID:grid.457334.2) (ISNI:0000 0001 0667 2738)