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“支原体抗原调节”,一种新型的表面变异,被认为是一种特定定位于支原体的脂蛋白。

"Mycoplasmal antigen modulation," a novel surface variation suggested for a lipoprotein specifically localized on Mycoplasma mobile.

机构信息

Department of Biology, Graduate School of Science, Osaka City University, Sumiyoshi-ku, Osaka 558-8585, Japan.

出版信息

Curr Microbiol. 2012 May;64(5):433-40. doi: 10.1007/s00284-012-0090-y. Epub 2012 Feb 15.

DOI:10.1007/s00284-012-0090-y
PMID:22349955
Abstract

Mycoplasma mobile, a pathogen of freshwater fish, glides easily across surfaces, colonizes on the fish gill, and causes necrosis. The cell surface is differentiated into three parts: the head, neck, and body. Mobile variable surface proteins (Mvsps) localizing at each of these parts may be involved in surface variation including phase variation and antigenic variation, although no proof exists. In this study, we examined this possibility by focusing on MvspI, the largest Mvsp. Immunofluorescence microscopy showed that MvspI is expressed on the surfaces of all cells. When anti-MvspI antibody was added at concentrations over 0.8 nM, MvspI was observed to decrease over time. After 72 h of cultivation with the antibody, the fluorescence intensity and amount of MvspI decreased up to 13 and 39%, respectively, compared to those of cells grown without antibody. These changes were reversed by the removal of the antibody. Such effects were not observed when another antibody targeting other Mvsps was used, suggesting that the decrease is specific to the relationship between MvspI and the antibody. Cell growth was also inhibited by the antibody, but the decrease in MvspI could not be explained by the selective growth of MvspI-negative variants or by the inhibition of growth with other conditions. The decrease in MvspI caused by the antibody binding may suggest a novel type of surface variation, designated here as "mycoplasmal antigen modulation."

摘要

滑动支原体是一种淡水鱼类病原体,能够轻松地在表面滑行,在鱼类鳃上定殖,并引起坏死。细胞表面分为三个部分:头部、颈部和身体。定位于这些部位的可移动表面蛋白(Mvsps)可能参与表面变异,包括相位变异和抗原变异,尽管没有证据证明。在这项研究中,我们通过关注最大的 Mvsp MvspI 来研究这种可能性。免疫荧光显微镜显示 MvspI 表达在所有细胞的表面。当添加的抗 MvspI 抗体浓度超过 0.8 nM 时,观察到 MvspI 随时间减少。与未添加抗体的细胞相比,在用抗体培养 72 小时后,MvspI 的荧光强度和数量分别减少了 13%和 39%。去除抗体后,这些变化得到逆转。当使用针对其他 Mvsps 的另一种抗体时,没有观察到这种变化,表明这种减少是 MvspI 与抗体之间的特异性关系所致。抗体也抑制了细胞生长,但 MvspI 的减少不能用 MvspI 阴性变体的选择性生长或其他条件下生长的抑制来解释。抗体结合引起的 MvspI 减少可能表明存在一种新型的表面变异,这里称为“支原体抗原调节”。

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Curr Microbiol. 2012 May;64(5):433-40. doi: 10.1007/s00284-012-0090-y. Epub 2012 Feb 15.
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Isolation and characterization of P1 adhesin, a leg protein of the gliding bacterium Mycoplasma pneumoniae.P1 黏附素的分离与鉴定,滑行细菌肺炎支原体的一种腿蛋白。
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Phase and antigenic variation in mycoplasmas.支原体的相位和抗原变异。
Future Microbiol. 2010 Jul;5(7):1073-85. doi: 10.2217/fmb.10.71.
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Unique centipede mechanism of Mycoplasma gliding.支原体滑行的独特蜈蚣机制。
高速原子力显微镜检测到移行支原体滑行机制的运动。
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Detailed Analyses of Stall Force Generation in Mycoplasma mobile Gliding.详细分析黏滑动支原体滑行中的阻力产生。
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Mycoplasma gallisepticum lipid associated membrane proteins up-regulate inflammatory genes in chicken tracheal epithelial cells via TLR-2 ligation through an NF-κB dependent pathway.鸡毒支原体脂相关膜蛋白通过TLR-2连接经NF-κB依赖途径上调鸡气管上皮细胞中的炎症基因。
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6
Localization of P42 and F(1)-ATPase α-subunit homolog of the gliding machinery in Mycoplasma mobile revealed by newly developed gene manipulation and fluorescent protein tagging.通过新开发的基因操作和荧光蛋白标记,揭示了滑行机制的 P42 和 F(1)-ATPase α 亚基同源物在黏支原体中的定位。
J Bacteriol. 2014 May;196(10):1815-24. doi: 10.1128/JB.01418-13. Epub 2014 Feb 7.
7
Whole surface image of Mycoplasma mobile, suggested by protein identification and immunofluorescence microscopy.运动支原体的整体表面图像,通过蛋白质鉴定和免疫荧光显微镜观察得到。
J Bacteriol. 2012 Nov;194(21):5848-55. doi: 10.1128/JB.00976-12. Epub 2012 Aug 24.
8
Molecular structure of isolated MvspI, a variable surface protein of the fish pathogen Mycoplasma mobile.孤立的 MvspI 的分子结构,鱼类病原体黏支原体的一种可变表面蛋白。
J Bacteriol. 2012 Jun;194(12):3050-7. doi: 10.1128/JB.00208-12. Epub 2012 Mar 23.
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4
Triskelion structure of the Gli521 protein, involved in the gliding mechanism of Mycoplasma mobile.Gli521 蛋白的三螺旋束结构,参与黏附运动型支原体的滑行机制。
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Centipede and inchworm models to explain Mycoplasma gliding.用于解释支原体滑行的蜈蚣和尺蠖模型。
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J Mol Evol. 2007 Sep;65(3):249-58. doi: 10.1007/s00239-007-9010-3. Epub 2007 Aug 9.
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A new promoterless reporter vector reveals antisense transcription in Mycoplasma genitalium.一种新的无启动子报告载体揭示了生殖支原体中的反义转录。
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