Soil and Water Science Department, University of Florida/Institute of Food and Agricultural Sciences, Gainesville, Florida, United States of America.
PLoS One. 2012;7(8):e42611. doi: 10.1371/journal.pone.0042611. Epub 2012 Aug 13.
Quorum sensing (QS) in Sinorhizobium meliloti involves at least half a dozen different N-acyl homoserine lactone (AHL) signals. These signals are produced by SinI, the sole AHL synthase in S. meliloti Rm8530. The sinI gene is regulated by two LuxR-type transcriptional regulators, SinR and ExpR. Mutations in sinI, sinR and expR abolish the production of exopolysaccharide II (EPS II).
METHODOLOGY/PRINCIPAL FINDINGS: This study investigated a new type of coordinated surface spreading of Rm8530 that can be categorized as swarming. Motility assays on semi-solid surfaces revealed that both flagella and EPS II are required for this type of motility. The production of EPS II depends on AHLs produced by SinI. Of these AHLs, only C(16:1)- and 3-oxo-C(16:1)-homoserine lactones (HSLs) stimulated swarming in an ExpR-dependent manner. These two AHLs induced the strongest response in the wggR reporter fusions. WggR is a positive regulator of the EPS II biosynthesis gene expression. The levels of the wggR activation correlated with the extent of swarming. Furthermore, swarming of S. meliloti required the presence of the high molecular weight (HMW) fraction of EPS II. Within swarming colonies, a recombinase-based RIVET reporter in the wggR gene was resolved in 30% of the cells, indicating an enhanced regulation of EPS II production in the subpopulation of cells, which was sufficient to support swarming of the entire colony.
CONCLUSIONS/SIGNIFICANCE: Swarming behavior of S. meliloti Rm8530 on semi-solid surfaces is found to be dependent on the functional QS regulatory cascades. Even though multiple AHL signals are produced by the bacterium, only two AHLs species, C(16:1)- and 3-oxo-C(16:1)-HSLs, affected swarming by up-regulating the expression of wggR. While EPS II is produced by Rm8530 as high and low molecular weight fractions, only the HMW EPS II facilitated initial stages of swarming, thus, suggesting a function for this polymer.
苜蓿中华根瘤菌中的群体感应(QS)至少涉及六种不同的 N-酰基高丝氨酸内酯(AHL)信号。这些信号由苜蓿中华根瘤菌 Rm8530 中唯一的 AHL 合酶 SinI 产生。sinI 基因受两个 LuxR 型转录调节因子 SinR 和 ExpR 调控。sinI、sinR 和 expR 的突变会导致多糖 II(EPS II)的产生减少。
方法/主要发现:本研究调查了 Rm8530 的一种新的表面协同扩散类型,可以归类为群体游动。在半固体表面的运动测定表明,鞭毛和 EPS II 都是这种运动类型所必需的。EPS II 的产生依赖于 SinI 产生的 AHL。在这些 AHL 中,只有 C(16:1)-和 3-氧代-C(16:1)-高丝氨酸内酯(HSL)以 ExpR 依赖的方式刺激群体游动。这两种 AHL 以最强的方式诱导 wggR 报告基因融合的反应。WggR 是 EPS II 生物合成基因表达的正调控因子。wggR 激活水平与群体游动程度相关。此外,苜蓿中华根瘤菌的群体游动需要 EPS II 的高分子量(HMW)部分。在群体游动菌落中,wggR 基因中的基于重组酶的 RIVET 报告基因在 30%的细胞中得到解决,表明细胞亚群中 EPS II 产生的调节增强,这足以支持整个菌落的群体游动。
结论/意义:发现苜蓿中华根瘤菌 Rm8530 在半固体表面的群体游动行为依赖于功能性 QS 调节级联。尽管细菌产生多种 AHL 信号,但只有两种 AHL 物种,C(16:1)-和 3-氧代-C(16:1)-HSL,通过上调 wggR 的表达来影响群体游动。虽然 Rm8530 产生高和低分子量的 EPS II,但只有 HMW EPS II 促进了群体游动的初始阶段,因此,这表明该聚合物具有功能。