Nakhamchik Alina, Wilde Caroline, Rowe-Magnus Dean A
Division of Clinical Integrative Biology, Sunnybrook Health Sciences Centre, 2075 Bayview Avenue, S1-26A, Toronto, Ontario, Canada M4N 3N5.
Infect Immun. 2007 Dec;75(12):5550-8. doi: 10.1128/IAI.00932-07. Epub 2007 Oct 8.
The estuarine bacterium Vibrio vulnificus is a human and animal pathogen. The expression of capsular polysaccharide (CPS) is essential for virulence. We used a new mini-Tn10 delivery vector, pNKTXI-SceI, to generate a mutant library and identify genes essential for CPS biosynthesis. Twenty-one acapsular mutants were isolated, and the disrupted gene in one mutant, coding for a polysaccharide polymerase (wzy), is described here. A wecA gene initiating glycosyltransferase was among the genes identified in the region flanking the wzy gene. This, together with the known structure of the CPS, supports a group IV capsule designation for the locus; however, its overall organization mirrored that of group I capsules. This new arrangement may be linked to our finding that the CPS region appears to have been recently acquired by horizontal transfer. Alcian Blue staining and immunoblotting with antisera against the wild-type strain indicated that the wzy::Tn10 mutant failed to produce CPS and was attenuated relative to the wild type in a septicemic mouse model. Interestingly, immunoblotting revealed that the mutant was also defective in lipopolysaccharide (LPS) production. However, the core-plus-one O-antigen pattern typical of wzy mutations was apparent. CPS production, LPS production, and virulence were restored following complementation with the wild-type wzy gene. Hence, Wzy participates in both CPS and LPS biosynthesis and is required for virulence in strain 27562. To our knowledge, this is the first functional demonstration of a Wzy polysaccharide polymerase in V. vulnificus and is the first to show a link between LPS and CPS biosynthesis.
河口细菌创伤弧菌是一种人畜共患病原体。荚膜多糖(CPS)的表达对其毒力至关重要。我们使用一种新的mini-Tn10递送载体pNKTXI-SceI构建了一个突变体文库,并鉴定了CPS生物合成所必需的基因。分离出21个无荚膜突变体,本文描述了其中一个突变体中编码多糖聚合酶(wzy)的基因被破坏的情况。在wzy基因侧翼区域鉴定出的基因中,有一个启动糖基转移酶的wecA基因。这与已知的CPS结构一起,支持将该基因座指定为IV型荚膜;然而,其整体组织与I型荚膜相似。这种新的排列可能与我们的发现有关,即CPS区域似乎是最近通过水平转移获得的。阿尔新蓝染色和用抗野生型菌株的抗血清进行免疫印迹表明,wzy::Tn10突变体未能产生CPS,并且在败血症小鼠模型中相对于野生型毒力减弱。有趣的是,免疫印迹显示该突变体在脂多糖(LPS)产生方面也存在缺陷。然而,wzy突变典型的核心加一个O抗原模式是明显的。用野生型wzy基因互补后,CPS产生、LPS产生和毒力得以恢复。因此,Wzy参与CPS和LPS的生物合成,并且是菌株27562毒力所必需的。据我们所知,这是创伤弧菌中Wzy多糖聚合酶的首次功能证明,也是首次表明LPS和CPS生物合成之间存在联系。