Maddula V S R K, Zhang Z, Pierson E A, Pierson L S
Division of Plant Pathology and Microbiology, Department of Plant Sciences, University of Arizona, Tucson, AZ 85721, USA.
Microb Ecol. 2006 Aug;52(2):289-301. doi: 10.1007/s00248-006-9064-6. Epub 2006 Aug 4.
The biological control bacterium Pseudomonas chlororaphis (aureofaciens) strain 30-84 employs two quorum sensing (QS) systems: PhzR/PhzI regulates the production of the antibiotics phenazine-1-carboxylic acid, 2-hydroxy-phenazine-1-carboxylic acid, and 2-hydroxy-phenazine, whereas CsaR/CsaI regulates currently unknown aspects of the cell surface. Previously characterized derivatives of strain 30-84 with mutations in each QS system and in the phenazine biosynthetic genes were screened for their ability to form surface-attached biofilm populations in vitro, using microtiter plate and flow cell biofilm assays, and on seeds and roots. Results from in vitro, seed, and root studies demonstrated that the PhzR/PhzI and the CsaR/CsaI QS regulatory systems contribute to the establishment of biofilms, with mutations in PhzR/PhzI having a significantly greater effect than mutations in CsaR/CsaI. Interestingly, phenazine antibiotic production was necessary for biofilm formation to the same extent as the PhzR/PhzI QS system, suggesting the loss of phenazines was responsible for the majority of the biofilm defect in these mutants. In vitro analysis indicated that genetic complementation or AHL addition to the growth medium restored the ability of the AHL synthase phzI mutant to form biofilms. However, only phenazine addition or genetic complementation of the phenazine biosynthetic mutation in trans restored biofilm formation by mutants defective in the transcriptional activator phzR or the phzB structural mutant. QS and phenazine production were also involved in the establishment of surface-attached populations on wheat seeds and plant roots, and, as observed in vitro, the addition of AHL extracts restored the ability of phzI mutants, but not phzR mutants, to form surface attached populations on seeds. Similarly, the presence of the wild type in mixtures with the mutants restored the ability of the mutants to colonize wheat roots, demonstrating that AHL and/or phenazine production by the wild-type population could complement the AHL- and phenazine-deficient mutants in situ. Together, these data demonstrate that both QS systems are involved in the formation of surface-attached populations required for biofilm formation by P. chlororaphis strain 30-84, and indicate a new role for phenazine antibiotics in rhizosphere community development beyond inhibition of other plant-associated microorganisms.
生防细菌绿针假单胞菌(金黄色变种)菌株30 - 84采用两种群体感应(QS)系统:PhzR/PhzI调控抗生素吩嗪 - 1 - 羧酸、2 - 羟基 - 吩嗪 - 1 - 羧酸和2 - 羟基吩嗪的产生,而CsaR/CsaI调控目前未知的细胞表面相关方面。利用微孔板和流动细胞生物膜测定法,以及在种子和根上,对先前表征的30 - 84菌株在每个QS系统和吩嗪生物合成基因中具有突变的衍生物进行体外形成表面附着生物膜群体能力的筛选。体外、种子和根研究的结果表明,PhzR/PhzI和CsaR/CsaI QS调控系统有助于生物膜的形成,PhzR/PhzI中的突变比CsaR/CsaI中的突变具有显著更大的影响。有趣的是,吩嗪抗生素的产生对于生物膜形成的必要性与PhzR/PhzI QS系统相同,这表明吩嗪的缺失是这些突变体中生物膜缺陷的主要原因。体外分析表明,对生长培养基进行遗传互补或添加AHL可恢复AHL合酶phzI突变体形成生物膜的能力。然而,只有添加吩嗪或对吩嗪生物合成突变进行反式遗传互补才能恢复转录激活因子phzR缺陷型突变体或phzB结构突变体的生物膜形成。QS和吩嗪产生也参与了小麦种子和植物根上表面附着群体的建立,并且,如在体外观察到的,添加AHL提取物可恢复phzI突变体而非phzR突变体在种子上形成表面附着群体的能力。同样,野生型与突变体混合时的存在恢复了突变体在小麦根上定殖的能力,表明野生型群体产生的AHL和/或吩嗪可以原位补充AHL和吩嗪缺陷型突变体。总之,这些数据表明,两个QS系统都参与了绿针假单胞菌菌株30 - 84形成生物膜所需的表面附着群体的形成,并表明吩嗪抗生素在根际群落发育中除了抑制其他植物相关微生物之外还有新的作用。