Department of Biology, California State University San Bernardino, San Bernardino, California, United States of America.
PLoS One. 2012;7(2):e31832. doi: 10.1371/journal.pone.0031832. Epub 2012 Feb 21.
Variovorax paradoxus is an aerobic soil bacterium associated with important biodegradative processes in nature. We use V. paradoxus EPS to study multicellular behaviors on surfaces.
We recovered flanking sequence from 123 clones in a Tn5 mutant library, with insertions in 29 different genes, selected based on observed surface behavior phenotypes. We identified three genes, Varpa_4665, Varpa_4680, and Varpa_5900, for further examination. These genes were cloned into pBBR1MCS2 and used to complement the insertion mutants. We also analyzed expression of Varpa_4680 and Varpa_5900 under different growth conditions by qPCR.
The 29 genes we identified had diverse predicted functions, many in exopolysaccharide synthesis. Varpa_4680, the most commonly recovered insertion site, encodes a putative N-acetyl-L-fucosamine transferase similar to WbuB. Expression of this gene in trans complemented the mutant fully. Several unique insertions were identified in Varpa_5900, which is one of three predicted pilY1 homologs in the EPS genome. No insertions in the two other putative pilY1 homologs present in the genome were identified. Expression of Varpa_5900 altered the structure of the wild type swarm, as did disruption of the chromosomal gene. The swarming phenotype was complemented by expression of Varpa_5900 from a plasmid, but biofilm formation was not restored. Both Varpa_4680 and Varpa_5900 transcripts were downregulated in biofilms and upregulated during swarming when compared to log phase culture. We identified a putative two component system (Varpa_4664-4665) encoding a response regulator (shkR) and a sensor histidine kinase (shkS), respectively. Biofilm formation increased and swarming was strongly delayed in the Varpa_4665 (shkS) mutant. Complementation of shkS restored the biofilm phenotype but swarming was still delayed. Expression of shkR in trans suppressed biofilm formation in either genetic background, and partially restored swarming in the mutant.
The data presented here point to complex regulation of these surface behaviors.
多变菌是一种好氧土壤细菌,与自然界中重要的生物降解过程有关。我们使用 V. paradoxus EPS 来研究表面上的多细胞行为。
我们从 Tn5 突变体文库中的 123 个克隆中回收了侧翼序列,这些插入物位于 29 个不同的基因中,是根据观察到的表面行为表型选择的。我们鉴定了三个基因,Varpa_4665、Varpa_4680 和 Varpa_5900,用于进一步研究。这些基因被克隆到 pBBR1MCS2 中,并用于互补插入突变体。我们还通过 qPCR 分析了不同生长条件下 Varpa_4680 和 Varpa_5900 的表达。
我们鉴定的 29 个基因具有不同的预测功能,许多与胞外多糖合成有关。Varpa_4680 是最常见的回收插入位点,编码一种类似 WbuB 的推定 N-乙酰-L-岩藻糖胺转移酶。该基因的表达在转基因中完全互补了突变体。在 EPS 基因组中三个预测的 pilY1 同源物之一的 Varpa_5900 中鉴定到几个独特的插入。在基因组中另外两个推定的 pilY1 同源物中没有鉴定到插入。Varpa_5900 的表达改变了野生型群集的结构,而染色体基因的破坏也是如此。Varpa_5900 的表达从质粒中得到了补充,但生物膜的形成没有恢复。与对数期培养相比,Varpa_4680 和 Varpa_5900 的转录本在生物膜中下调,在 swarm 时上调。我们鉴定了一个推定的双组分系统(Varpa_4664-4665),分别编码一个响应调节剂(shkR)和一个传感器组氨酸激酶(shkS)。Varpa_4665(shkS)突变体中的生物膜形成增加,swarm 延迟强烈。shkS 的互补恢复了生物膜表型,但 swarm 仍然延迟。shkR 的表达在转基因中抑制了两种遗传背景下的生物膜形成,并部分恢复了突变体中的 swarm。
这里提出的数据表明这些表面行为的复杂调控。