Quorum-Quenching Bacteria Isolated From Red Sea Sediments Reduce Biofilm Formation by Pseudomonas aeruginosa

被引:80
作者
Rehman, Zahid Ur [1 ]
Leiknes, TorOve [1 ]
机构
[1] King Abdullah Univ Sci & Technol, Water Desalinat & Reuse Ctr, Thuwal, Saudi Arabia
关键词
quorum quenching; marine bacteria; N-acylhomoserine lactone degradation; Red Sea sediments; biofilm inhibition; LACTONE-DEGRADING BACTERIA; SP-NOV; AHL-LACTONASE; GEN; NOV; IN-VITRO; INHIBIT; IDENTIFICATION; COLONIZATION; DIVERSITY; INFECTION;
D O I
10.3389/fmicb.2018.01354
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Quorum sensing (QS) is the process by which bacteria communicate with each other through small signaling molecules such as N-acylhomoserine lactones (AHLs). Certain bacteria can degrade AHL molecules by a process called quorum quenching (QQ); therefore, QQ can be used to control bacterial infections and biofilm formation. In this study, we aimed to identify new species of bacteria with QQ activity. Red Sea sediments were collected either from the close vicinity of seagrass or from areas with no vegetation. We isolated 72 bacterial strains, which were tested for their ability to degrade/inactivate AHL molecules. Chromobacterium violaceum CV026-based bioassay was used for the initial screening of isolates with QQ activity. QQ activity was further quantified using high-performance liquid chromatography-tandem mass spectrometry. We found that these isolates could degrade AHL molecules of different acyl chain lengths as well as modifications. 16S-rRNA sequencing of positive QQ isolates showed that they belonged to three different genera. Specifically, two isolates belonged to the genus Erythrobacter; four, Labrenzia; and one, Bacterioplanes. The genome of one representative isolate from each genus was sequenced, and potential QQ enzymes, namely, lactonases and acylases, were identified. The ability of these isolates to degrade the 30XOC12-AHLs produced by Pseudomonas aeruginosa PAO1 and hence inhibit biofilm formation was investigated. Our results showed that the isolate VG12 (genus Labrenzia) is better than other isolates at controlling biofilm formation by PAO1 and degradation of different AHL molecules. Time-course experiments to study AHL degradation showed that VG1 (genus Erythrobacter) could degrade AHLs faster than other isolates. Thus, QQ bacteria or enzymes can be used in combination with an antibacterial to overcome antibiotic resistance.
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