Department of Hematology and Oncology L, and A, Seragnoli, University St, Orsola-Malpighi Hospital, V, Massarenti 9, Bologna, Italy.
BMC Infect Dis. 2010 Dec 7;10:345. doi: 10.1186/1471-2334-10-345.
Treponema denticola is an oral spirochete involved in the pathogenesis and progression of periodontal disease. Of its virulence factors, the major surface protein (MSP) plays a role in the interaction between the treponeme and host. To understand the possible evolution of this protein, we analyzed the sequence of the msp gene in 17 T. denticola positive clinical samples.
Nucleotide and amino acid sequence of MSP have been determined by PCR amplification and sequencing in seventeen T. denticola clinical specimens to evaluate the genetic variability and the philogenetic relationship of the T. denticola msp gene among the different amplified sequence of positive samples. In silico antigenic analysis was performed on each MSP sequences to determined possible antigenic variation.
The msp sequences showed two highly conserved 5' and 3' ends and a central region that varies substantially. Phylogenetic analysis categorized the 17 specimens into 2 principal groups, suggesting a low rate of evolutionary variability and an elevated degree of conservation of msp in clinically derived genetic material. Analysis of the predicted antigenic variability between isolates, demonstrated that the major differences lay between amino acids 200 and 300.
These findings showed for the first time, the nucleotide and amino acids variation of the msp gene in infecting T. denticola, in vivo. This data suggested that the antigenic variability found in to the MSP molecule, may be an important factor involved in immune evasion by T. denticola.
牙龈密螺旋体是一种口腔螺旋体,参与牙周病的发病和进展。在其毒力因子中,主要表面蛋白(MSP)在密螺旋体与宿主之间的相互作用中起作用。为了了解该蛋白的可能进化,我们分析了 17 个 T. denticola 阳性临床样本中的 msp 基因序列。
通过 PCR 扩增和测序确定了 17 个 T. denticola 临床标本中 MSP 的核苷酸和氨基酸序列,以评估不同阳性标本扩增序列中 T. denticola msp 基因的遗传变异性和系统发育关系。对每个 MSP 序列进行了计算机模拟抗原分析,以确定可能的抗原变异。
msp 序列显示出两个高度保守的 5'和 3'末端和一个变化很大的中央区域。系统发育分析将 17 个标本分为 2 个主要组,表明进化变异率低,msp 在临床衍生遗传物质中的保守程度高。对分离株之间预测的抗原变异性的分析表明,主要差异在于 200 到 300 位氨基酸。
这些发现首次显示了感染 T. denticola 中 msp 基因的核苷酸和氨基酸变异。这些数据表明,MSP 分子中发现的抗原变异性可能是 T. denticola 免疫逃避的一个重要因素。