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主要抗原蛋白Msp和TmpC存在缺陷的齿垢密螺旋体突变体的特性分析

Characterization of Treponema denticola mutants defective in the major antigenic proteins, Msp and TmpC.

作者信息

Abiko Yuki, Nagano Keiji, Yoshida Yasuo, Yoshimura Fuminobu

机构信息

Department of Microbiology, School of Dentistry, Aichi Gakuin University Nagoya, Aichi, Japan.

出版信息

PLoS One. 2014 Nov 17;9(11):e113565. doi: 10.1371/journal.pone.0113565. eCollection 2014.

DOI:10.1371/journal.pone.0113565
PMID:25401769
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4234677/
Abstract

Treponema denticola, a gram-negative and anaerobic spirochete, is associated with advancing severity of chronic periodontitis. In this study, we confirmed that two major antigenic proteins were Msp and TmpC, and examined their physiological and pathological roles using gene-deletion mutants. Msp formed a large complex that localized to the outer membrane, while TmpC existed as a monomer and largely localized to the inner membrane. However, TmpC was also detected in the outer membrane fraction, but its cell-surface exposure was not detected. Msp defects increased cell-surface hydrophobicity and secretion of TNF-α from macrophage-like cells, whereas TmpC defects decreased autoagglutination and chymotrypsin-like protease activities. Both mutants adhered to gingival epithelial cells similarly to the wild-type and showed slightly decreased motility. In addition, in Msp-defective mutants, the TDE1072 protein, which is a major membrane protein, was abolished; therefore, phenotypic changes in the mutant can be, at least in part, attributed to the loss of the TDE1072 protein. Thus, the major antigenic proteins, Msp and TmpC, have significant and diverse impacts on the characteristics of T. denticola, especially cell surface properties.

摘要

齿垢密螺旋体是一种革兰氏阴性厌氧螺旋体,与慢性牙周炎病情的进展相关。在本研究中,我们证实了两种主要抗原蛋白为Msp和TmpC,并使用基因缺失突变体研究了它们的生理和病理作用。Msp形成一个定位于外膜的大型复合物,而TmpC以单体形式存在,主要定位于内膜。然而,在外膜组分中也检测到了TmpC,但未检测到其细胞表面暴露。Msp缺陷增加了细胞表面疏水性以及巨噬细胞样细胞中TNF-α的分泌,而TmpC缺陷降低了自凝作用和类胰凝乳蛋白酶活性。两种突变体与野生型一样能类似地黏附于牙龈上皮细胞,且运动性略有降低。此外,在Msp缺陷突变体中,主要膜蛋白TDE1072蛋白缺失;因此,突变体中的表型变化至少部分可归因于TDE1072蛋白的缺失。因此,主要抗原蛋白Msp和TmpC对齿垢密螺旋体的特性,尤其是细胞表面特性,具有显著且多样的影响。

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PLoS One. 2014 Feb 21;9(2):e89051. doi: 10.1371/journal.pone.0089051. eCollection 2014.
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A surface-exposed neuraminidase affects complement resistance and virulence of the oral spirochaete Treponema denticola.表面暴露的神经氨酸酶影响口腔螺旋体齿密螺旋体的补体抗性和毒力。
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The major outer sheath protein (Msp) of Treponema denticola has a bipartite domain architecture and exists as periplasmic and outer membrane-spanning conformers.
齿密螺旋体刺激中性粒细胞和巨噬细胞释放和从头合成肿瘤坏死因子 M 细胞因子。
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The Msp Protein of Treponema denticola Interrupts Activity of Phosphoinositide Processing in Neutrophils.牙龈密螺旋体 Msp 蛋白中断中性粒细胞中磷酯酰肌醇代谢。
Infect Immun. 2019 Oct 18;87(11). doi: 10.1128/IAI.00553-19. Print 2019 Nov.
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Microenvironment of Culture to Induce Cholesterol Consumption Does Cell Wall Remodeling and Enables the Formation of Granuloma-Like Structures.培养环境诱导胆固醇摄取会进行细胞壁重塑,并有助于肉芽肿样结构的形成。
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Oral microbiome and peri-implant diseases: where are we now?口腔微生物群与种植体周围疾病:我们目前的进展如何?
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The C-terminal region of the major outer sheath protein of Treponema denticola inhibits neutrophil chemotaxis.齿垢密螺旋体主要外鞘蛋白的C末端区域可抑制中性粒细胞趋化性。
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The Treponema denticola FhbB Protein Is a Dominant Early Antigen That Elicits FhbB Variant-Specific Antibodies That Block Factor H Binding and Cleavage by Dentilisin.齿垢密螺旋体FhbB蛋白是一种主要的早期抗原,可引发FhbB变体特异性抗体,这些抗体可阻断补体因子H与牙蛋白酶的结合及裂解。
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A simplified erythromycin resistance cassette for Treponema denticola mutagenesis.用于密螺旋体属变异的简化红霉素抗性盒。
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Treponema denticola PrcB is required for expression and activity of the PrcA-PrtP (dentilisin) complex.齿垢密螺旋体 PrcB 对于 PrcA-PrtP(齿龈蛋白酶)复合物的表达和活性是必需的。
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