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Biofilm formation assessment in Sinorhizobium meliloti reveals interlinked control with surface motility

机译:苜蓿中华根瘤菌的生物膜形成评估表明,相互联系的控制与表面运动

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Background Swarming motility and biofilm formation are opposite, but related surface-associated behaviors that allow various pathogenic bacteria to colonize and invade their hosts. In Sinorhizobium meliloti, the alfalfa endosymbiont, these bacterial processes and their relevance for host plant colonization are largely unexplored. Our previous work demonstrated distinct swarming abilities in two S. meliloti strains (Rm1021 and GR4) and revealed that both environmental cues (iron concentration) and bacterial genes (fadD, rhb, rirA) play crucial roles in the control of surface motility in this rhizobial species. In the current study, we investigate whether these factors have an impact on the ability of S. meliloti to establish biofilms and to colonize host roots. Results We found that strain GR4, which is less prone to translocate on solid surfaces than strain Rm1021, is more efficient in developing biofilms on glass and plant root surfaces. High iron conditions, known to prevent surface motility in a wild-type strain of S. meliloti, promote biofilm development in Rm1021 and GR4 strains by inducing the formation of more structured and thicker biofilms than those formed under low iron levels. Moreover, three different S. meliloti mutants (fadD, rhb, and rirA) that exhibit an altered surface translocation behavior compared with the wild-type strain, establish reduced biofilms on both glass and alfalfa root surfaces. Iron-rich conditions neither rescue the defect in biofilm formation shown by the rhb mutant, which is unable to produce the siderophore rhizobactin 1021 (Rhb1021), nor have any impact on biofilms formed by the iron-response regulator rirA mutant. On the other hand, S. meliloti FadD loss-of-function mutants do not establish normal biofilms irrespective of iron levels. Conclusions Our studies show that siderophore Rhb1021 is not only required for surface translocation, but also for biofilm formation on glass and root surfaces by strain Rm1021. In addition, we present evidence for the existence of control mechanisms that inversely regulate swarming and biofilm formation in S. meliloti, and that contribute to efficient plant root colonization. One of these mechanisms involves iron levels and the iron global regulator RirA. The other mechanism involves the participation of the fatty acid metabolism-related enzyme FadD.
机译:背景成群运动和生物膜形成是相反的,但是相关的表面相关行为使各种病原细菌能够定居并侵入其宿主。在苜蓿中华根瘤菌(Sinorhizobium meliloti)中,紫花苜蓿内共生体的这些细菌过程及其与寄主植物定植的相关性尚未得到充分研究。我们以前的工作证明了两种苜蓿链球菌菌株(Rm1021和GR4)具有独特的群聚能力,并且揭示了环境线索(铁浓度)和细菌基因(fadD,rhb,rirA)均在控制该根瘤菌的表面运动中起着至关重要的作用。种类。在当前的研究中,我们调查这些因素是否对S. meliloti建立生物膜和定殖宿主根的能力有影响。结果我们发现GR4菌株比Rm1021菌株更不易在固体表面上转移,它在玻璃和植物根部表面上形成生物膜的效率更高。已知高铁条件可防止野生葡萄球菌的表面运动,它通过诱导比低铁水平下形成的生物膜更结构化和更厚的生物膜的形成,促进了Rm1021和GR4菌株中生物膜的发育。此外,与野生型菌株相比,表现出改变的表面易位行为的三个不同的苜蓿链球菌突变体(fadD,rhb和rirA)在玻璃和苜蓿根表面均建立了减少的生物膜。富铁条件既不能挽救无法产生铁载体根瘤菌素1021(Rhb1021)的rhb突变体显示的生物膜形成缺陷,也不会对铁反应调节剂rirA突变体形成的生物膜产生任何影响。另一方面,无论铁水平如何,S。meliloti FadD功能丧失的突变体都无法建立正常的生物膜。结论我们的研究表明,铁载体Rhb1021不仅是表面转运所必需的,而且是菌株Rm1021在玻璃和根部表面上形成生物膜的必需物质。另外,我们提供证据证明存在控制机制,该控制机制反向调节蜂群中的蜂群和生物膜形成,并有助于有效的植物根部定植。这些机制之一涉及铁水平和铁全局调节剂RirA。另一机制涉及脂肪酸代谢相关酶FadD的参与。

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