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PA2663(PpyR)通过psl操纵子增加铜绿假单胞菌PAO1中的生物膜形成,并刺激毒力和群体感应表型。

PA2663 (PpyR) increases biofilm formation in Pseudomonas aeruginosa PAO1 through the psl operon and stimulates virulence and quorum-sensing phenotypes.

作者信息

Attila Can, Ueda Akihiro, Wood Thomas K

机构信息

Artie McFerrin Department of Chemical Engineering, Texas A & M University, College Station, TX, 77843-3122, USA.

出版信息

Appl Microbiol Biotechnol. 2008 Feb;78(2):293-307. doi: 10.1007/s00253-007-1308-y. Epub 2007 Dec 22.

Abstract

Previously, we identified the uncharacterized predicted membrane protein PA2663 of Pseudomonas aeruginosa PAO1 as a virulence factor using a poplar tree model; PA2663 was induced in the poplar rhizosphere and, upon inactivation, it caused 20-fold lower biofilm formation (Attila et al., Microb Biotechnol, 2008). Here, we confirmed that PA2663 is related to biofilm formation by restoring the wild-type phenotype by complementing the PA2663 mutation in trans and investigated the genetic basis of its influence on biofilm formation through whole-transcriptome and -phenotype studies. Upon inactivating PA2663 by transposon insertion, the psl operon that encodes a galactose- and mannose-rich exopolysaccharide was highly repressed (verified by RT-PCR). The inactivation of PA2663 also repressed 13 pyoverdine genes, which eliminated the production of the virulence factor pyoverdine in P. aeruginosa. The inactivation of PA2663 also affected other quorum-sensing-related phenotypes in that it repressed the Pseudomonas quinolone signal (PQS) genes, which abolished PQS production, and repressed lasB, which decreased elastase activity sevenfold. Genes were also induced for motility and attachment (PA0499, PA0993, PA2130, and PA4549) and for small molecule transport (PA0326, PA1541, PA1632, PA1971, PA2214, PA2215, PA2678, and PA3407). Phenotype arrays also showed that PA2663 represses growth on D: -gluconic acid, D: -mannitol, and N-phthaloyl-L: -glutamic acid. Hence, the PA2663 gene product increases biofilm formation by increasing the psl-operon-derived exopolysaccharides and increases pyoverdine synthesis, PQS production, and elastase activity while reducing swarming and swimming motility. We speculate that PA2663 performs these myriad functions as a novel membrane sensor.

摘要

此前,我们利用杨树模型将铜绿假单胞菌PAO1中未表征的预测膜蛋白PA2663鉴定为一种毒力因子;PA2663在杨树根际中被诱导,失活后,其生物膜形成能力降低了20倍(阿提拉等人,《微生物生物技术》,2008年)。在此,我们通过反式互补PA2663突变恢复野生型表型,证实PA2663与生物膜形成有关,并通过全转录组和表型研究探究了其影响生物膜形成的遗传基础。通过转座子插入使PA2663失活后,编码富含半乳糖和甘露糖的胞外多糖的psl操纵子受到高度抑制(通过RT-PCR验证)。PA2663的失活还抑制了13个绿脓菌素基因,这消除了铜绿假单胞菌中毒力因子绿脓菌素的产生。PA2663的失活还影响了其他与群体感应相关的表型,因为它抑制了假单胞菌喹诺酮信号(PQS)基因,从而消除了PQS的产生,并抑制了lasB,使弹性蛋白酶活性降低了七倍。还诱导了与运动性和附着相关的基因(PA0499、PA0993、PA2130和PA4549)以及与小分子转运相关的基因(PA0326、PA1541、PA1632、PA1971、PA2214、PA2215、PA2678和PA3407)。表型阵列还显示,PA2663抑制在D-葡萄糖酸、D-甘露醇和N-邻苯二甲酰-L-谷氨酸上的生长。因此,PA2663基因产物通过增加psl操纵子衍生的胞外多糖来增加生物膜形成,并增加绿脓菌素合成、PQS产生和弹性蛋白酶活性,同时降低群体游动和游泳运动性。我们推测PA2663作为一种新型膜传感器发挥这些众多功能。

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