Analysis of Streptococcus mutans biofilm proteins recognized by salivary immunoglobulin A.

T Sanui, R L Gregory
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引用次数: 29

Abstract

Introduction: The purpose of this study was to examine the Streptococcus mutans biofilm cellular proteins recognized by immunoglobulin A (IgA) in saliva from various caries-defined populations.

Methods: Biofilm and planktonic S. mutans UA159 cells were prepared. The proteins were extracted, separated by two-dimensional gel electrophoresis, transferred to blotting membranes, and probed for IgA using individual saliva samples from three groups of subjects; those who developed 0 caries (no active caries), 5-9 caries (medium), or more than 10 caries (severe) over a 12-month interval.

Results: Several proteins were recognized by salivary IgA in all groups of saliva but spot distribution and intensity varied greatly between the groups, and some proteins were recognized more strongly in biofilm cells than in planktonic culture, and vice versa. Furthermore, 15 proteins were only recognized by saliva from the 'no active caries' group, and four proteins were recognized by saliva samples from subjects in all three groups. Specifically, antigen I/II was recognized less in biofilm cells by caries-free saliva compared with planktonic cells. However, salivary IgA antibody to antigen I/II was absent in blots using saliva from the 'medium caries' and 'severe caries' groups.

Conclusion: The bacterial molecules recognized by caries-free saliva are significant factors for S. mutans caries formation, and their inhibition could be a therapeutic target. In addition, saliva of caries-free subjects includes significant IgA antibody against antigen I/II of S. mutans, indicating a protective mechanism. However, microorganisms may protect themselves from host immune attack by forming biofilms and decreasing expression of antigen I/II.

唾液免疫球蛋白A识别的变形链球菌生物膜蛋白分析。
本研究的目的是检测不同龋齿人群唾液中变形链球菌生物膜细胞蛋白被免疫球蛋白A (IgA)识别的情况。方法:制备生物膜和浮游变形链球菌UA159细胞。提取蛋白质,通过二维凝胶电泳分离,转移到印迹膜上,并使用来自三组受试者的个体唾液样本探测IgA;在12个月的时间间隔内,0个龋齿(无活动性龋齿)、5-9个龋齿(中等)或10个以上龋齿(严重)的人。结果:有几种蛋白在各组唾液中均可被唾液IgA识别,但斑点分布和强度在各组间差异较大,部分蛋白在生物膜细胞中的识别强于在浮游培养中的识别,反之亦然。此外,15种蛋白质仅被“无活性龋齿”组的唾液识别,4种蛋白质被所有三组受试者的唾液样本识别。具体而言,与浮游细胞相比,无龋生物膜细胞的唾液对抗原I/II的识别较少。然而,在使用“中度龋齿”组和“严重龋齿”组唾液进行印迹检测时,唾液中没有针对抗原I/II的IgA抗体。结论:无龋唾液识别的细菌分子是变形链球菌龋齿形成的重要因素,抑制这些细菌分子可能是治疗的靶点。此外,无龋受试者唾液中含有显著的针对突变链球菌抗原I/II的IgA抗体,提示其保护机制。然而,微生物可能通过形成生物膜和降低抗原I/II的表达来保护自己免受宿主免疫攻击。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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