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本文引用的文献

1
Structure-function analysis of the self-recognizing Antigen 43 autotransporter protein from Escherichia coli.来自大肠杆菌的自我识别抗原43自转运蛋白的结构-功能分析
Mol Microbiol. 2004 Jan;51(1):283-96. doi: 10.1046/j.1365-2958.2003.03833.x.
2
Multiple elements controlling adherence of enterohemorrhagic Escherichia coli O157:H7 to HeLa cells.多种控制肠出血性大肠杆菌O157:H7对HeLa细胞黏附的因素。
Infect Immun. 2003 Sep;71(9):4985-95. doi: 10.1128/IAI.71.9.4985-4995.2003.
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Intracellular bacterial biofilm-like pods in urinary tract infections.尿路感染中的细胞内细菌生物膜样荚膜
Science. 2003 Jul 4;301(5629):105-7. doi: 10.1126/science.1084550.
4
Development and maturation of Escherichia coli K-12 biofilms.大肠杆菌K-12生物膜的发育与成熟
Mol Microbiol. 2003 May;48(4):933-46. doi: 10.1046/j.1365-2958.2003.03490.x.
5
Global gene expression in Escherichia coli biofilms.大肠杆菌生物膜中的全基因组表达
Mol Microbiol. 2003 Apr;48(1):253-67. doi: 10.1046/j.1365-2958.2003.03432.x.
6
Differential expression of the Escherichia coli autoaggregation factor antigen 43.大肠杆菌自聚集因子抗原43的差异表达
J Bacteriol. 2003 Apr;185(7):2236-42. doi: 10.1128/JB.185.7.2236-2242.2003.
7
Role of capsule in Klebsiella pneumoniae virulence: lack of correlation between in vitro and in vivo studies.荚膜在肺炎克雷伯菌毒力中的作用:体外研究与体内研究之间缺乏相关性。
FEMS Microbiol Lett. 2003 Jan 21;218(1):149-54. doi: 10.1111/j.1574-6968.2003.tb11511.x.
8
DNA microarray analysis of fim mutations in Escherichia coli.大肠杆菌中菌毛突变的DNA微阵列分析。
Mol Genet Genomics. 2002 Aug;267(6):721-9. doi: 10.1007/s00438-002-0705-2. Epub 2002 Jun 21.
9
Characterization of Cah, a calcium-binding and heat-extractable autotransporter protein of enterohaemorrhagic Escherichia coli.肠出血性大肠杆菌的钙结合且热可提取自转运蛋白Cah的特性分析
Mol Microbiol. 2002 Aug;45(4):951-66. doi: 10.1046/j.1365-2958.2002.03094.x.
10
Antigen 43-mediated autotransporter display, a versatile bacterial cell surface presentation system.抗原43介导的自转运体展示,一种通用的细菌细胞表面呈递系统。
J Bacteriol. 2002 Aug;184(15):4197-204. doi: 10.1128/JB.184.15.4197-4204.2002.

荚膜可保护短细菌黏附素的功能。

Capsule shields the function of short bacterial adhesins.

作者信息

Schembri Mark A, Dalsgaard Dorte, Klemm Per

机构信息

Microbial Adhesion Group, BioCentrum-DTU, Technical University of Denmark, DK-2800 Lyngby, Denmark.

出版信息

J Bacteriol. 2004 Mar;186(5):1249-57. doi: 10.1128/JB.186.5.1249-1257.2004.

DOI:10.1128/JB.186.5.1249-1257.2004
PMID:14973035
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC344426/
Abstract

Bacterial surface structures such as capsules and adhesins are generally regarded as important virulence factors. Here we demonstrate that capsules block the function of the self-recognizing protein antigen 43 through physical shielding. The phenomenon is not restricted to Escherichia coli but can occur in other gram-negative bacteria. Likewise, we show that other short adhesins exemplified by the AIDA-I protein are blocked by the presence of a capsule. The results support the notion that capsule polysaccharides sterically prevent receptor-target recognition of short bacterial adhesins. This negative interference has important biological consequences, such as affecting the ability of bacteria to form biofilms.

摘要

诸如荚膜和粘附素等细菌表面结构通常被视为重要的毒力因子。在此我们证明,荚膜通过物理屏蔽作用阻断了自我识别蛋白抗原43的功能。这种现象并不局限于大肠杆菌,在其他革兰氏阴性菌中也可能发生。同样,我们表明,以AIDA-I蛋白为代表的其他短粘附素也会因荚膜的存在而被阻断。这些结果支持了这样一种观点,即荚膜多糖在空间上阻止了细菌短粘附素与受体的靶向识别。这种负面干扰具有重要的生物学后果,比如影响细菌形成生物膜的能力。