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生物膜形成增强及荚膜合成丧失:牙龈卟啉单胞菌中一个假定糖基转移酶的缺失

Enhanced biofilm formation and loss of capsule synthesis: deletion of a putative glycosyltransferase in Porphyromonas gingivalis.

作者信息

Davey Mary E, Duncan Margaret J

机构信息

Department of Molecular Genetics, The Forsyth Institute, 140 The Fenway, Boston, MA 02115, USA.

出版信息

J Bacteriol. 2006 Aug;188(15):5510-23. doi: 10.1128/JB.01685-05.

Abstract

Periodontitis is a biofilm-mediated disease. Porphyromonas gingivalis is an obligate anaerobe consistently associated with severe manifestations of this disease. As an opportunistic pathogen, the ability to proliferate within and disseminate from subgingival biofilm (plaque) is central to its virulence. Here, we report the isolation of a P. gingivalis transposon insertion mutant altered in biofilm development and the reconstruction and characterization of this mutation in three different wild-type strains. The mutation responsible for the altered biofilm phenotype was in a gene with high sequence similarity ( approximately 61%) to a glycosyltransferase gene. The gene is located in a region of the chromosome that includes up to 16 genes predicted to be involved in the synthesis and transport of capsular polysaccharide. The phenotype of the reconstructed mutation in all three wild-type backgrounds is that of enhanced biofilm formation. In addition, in strain W83, a strain that is encapsulated, the glycosyltransferase mutation resulted in a loss of capsule. Further experiments showed that the W83 mutant strain was more hydrophobic and exhibited increased auto-aggregation. Our results indicate that we have identified a gene involved in capsular-polysaccharide synthesis in P. gingivalis and that the production of capsule prevented attachment and the initiation of in vitro biofilm formation on polystyrene microtiter plates.

摘要

牙周炎是一种由生物膜介导的疾病。牙龈卟啉单胞菌是一种专性厌氧菌,一直与该疾病的严重表现相关。作为一种机会致病菌,在龈下生物膜(菌斑)内增殖并从其中扩散的能力是其毒力的核心。在此,我们报告了一株牙龈卟啉单胞菌转座子插入突变体的分离,该突变体在生物膜形成方面发生改变,以及在三种不同野生型菌株中对该突变的重建和表征。导致生物膜表型改变的突变存在于一个与糖基转移酶基因序列相似度较高(约61%)的基因中。该基因位于染色体的一个区域,该区域包含多达16个预计参与荚膜多糖合成和转运的基因。在所有三种野生型背景下重建突变的表型均为生物膜形成增强。此外,在有荚膜的W83菌株中,糖基转移酶突变导致荚膜丧失。进一步的实验表明,W83突变菌株疏水性更强,且自聚集增加。我们的结果表明,我们已经鉴定出牙龈卟啉单胞菌中一个参与荚膜多糖合成的基因,并且荚膜的产生阻止了在聚苯乙烯微量滴定板上的附着和体外生物膜形成的起始。

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