首页> 外文期刊>Molecular Microbiology >A complex LuxR-LuxI type quorum sensing network in a roseobacterial marine sponge symbiont activates flagellar motility and inhibits biofilm formation
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A complex LuxR-LuxI type quorum sensing network in a roseobacterial marine sponge symbiont activates flagellar motility and inhibits biofilm formation

机译:玫瑰细菌海洋海绵共生物中的复杂LuxR-LuxI型群体感应网络激活鞭毛运动并抑制生物膜形成

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Bacteria isolated from marine sponges, including the Silicibacter-Ruegeria (SR) subgroup of the Roseobacter clade, produce N-acylhomoserine lactone (AHL) quorum sensing signal molecules. This study is the first detailed analysis of AHL quorum sensing in sponge-associated bacteria, specifically Ruegeria sp. KLH11, from the sponge Mycale laxissima. Two pairs of luxR and luxI homologues and one solo luxI homologue were identified and designated ssaRI, ssbRI and sscI (sponge-associated symbiont locus A, B and C, luxR or luxI homologue). SsaI produced predominantly long-chain 3-oxo-AHLs and both SsbI and SscI specified 3-OH-AHLs. Addition of exogenous AHLs to KLH11 increased the expression of ssaI but not ssaR, ssbI or ssbR, and genetic analyses revealed a complex interconnected arrangement between SsaRI and SsbRI systems. Interestingly, flagellar motility was abolished in the ssaI and ssaR mutants, with the flagellar biosynthesis genes under strict SsaRI control, and active motility only at high culture density. Conversely, ssaI and ssaR mutants formed more robust biofilms than wild-type KLH11. AHLs and the ssaI transcript were detected in M.laxissima extracts, suggesting that AHL signalling contributes to the decision between motility and sessility and that it may also facilitate acclimation to different environments that include the sponge host.
机译:从海洋海绵中分离出的细菌,包括玫瑰杆菌属的Silicibacter-Ruegeria(SR)亚组,可产生N-酰基高丝氨酸内酯(AHL)群体感应信号分子。这项研究是海绵相关细菌,特别是Ruegeria sp。中AHL群体感应的首次详细分析。 KLH11,来自海绵Mycale laxissima。鉴定了两对luxR和luxI同源物以及一个单独的luxI同源物,并命名为ssaRI,ssbRI和sscI(与海绵相关的共生基因座A,B和C,luxR或luxI同源物)。 SsaI主要产生长链3-oxo-AHL,而SsbI和SscI均指定了3-OH-AHL。向KLH11中添加外源AHL可增加ssaI的表达,但不会增加ssaR,ssbI或ssbR的表达,遗传分析显示SsaRI和SsbRI系统之间存在复杂的相互联系的安排。有趣的是,ssaI和ssaR突变体废除了鞭毛运动,鞭毛生物合成基因受到严格的SsaRI控制,仅在高培养密度下才具有主动运动。相反,ssaI和ssaR突变体比野生型KLH11形成更坚固的生物膜。在M.laxissima提取物中检测到AHL和ssaI转录物,这表明AHL信号有助于决定运动性与固性之间的关系,也可能有助于适应包括海绵宿主在内的不同环境。

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