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2
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本文引用的文献

1
Identification and cell cycle control of a novel pilus system in Caulobacter crescentus.新月柄杆菌中一种新型菌毛系统的鉴定及细胞周期调控
EMBO J. 2000 Jul 3;19(13):3223-34. doi: 10.1093/emboj/19.13.3223.
2
Tenacious adhesion of Actinobacillus actinomycetemcomitans strain CU1000 to salivary-coated hydroxyapatite.伴放线放线杆菌CU1000菌株对唾液包被的羟基磷灰石的牢固黏附。
Arch Oral Biol. 1999 Dec;44(12):1063-76. doi: 10.1016/s0003-9969(99)00089-8.
3
Direct selection of IS903 transposon insertions by use of a broad-host-range vector: isolation of catalase-deficient mutants of Actinobacillus actinomycetemcomitans.利用广宿主范围载体直接选择IS903转座子插入:放线共生放线杆菌过氧化氢酶缺陷型突变体的分离
J Bacteriol. 1999 Dec;181(23):7298-307. doi: 10.1128/JB.181.23.7298-7307.1999.
4
Virulence factors of Actinobacillus actinomycetemcomitans.伴放线放线杆菌的毒力因子
Periodontol 2000. 1999 Jun;20:136-67. doi: 10.1111/j.1600-0757.1999.tb00161.x.
5
Actinobacillus actinomycetemcomitans and Porphyromonas gingivalis in nonoral infections.伴放线放线杆菌与牙龈卟啉单胞菌在非口腔感染中的情况
Periodontol 2000. 1999 Jun;20:122-35. doi: 10.1111/j.1600-0757.1999.tb00160.x.
6
Actinobacillus actinomycetemcomitans and Porphyromonas gingivalis in human periodontal disease: occurrence and treatment.人类牙周病中的伴放线放线杆菌和牙龈卟啉单胞菌:发生率与治疗
Periodontol 2000. 1999 Jun;20:82-121. doi: 10.1111/j.1600-0757.1999.tb00159.x.
7
Phenotypic variation in Actinobacillus actinomycetemcomitans during laboratory growth: implications for virulence.伴放线放线杆菌在实验室培养过程中的表型变异:对毒力的影响
Microbiology (Reading). 1999 Jun;145 ( Pt 6):1335-1347. doi: 10.1099/13500872-145-6-1335.
8
Identification and molecular analysis of rough-colony-specific outer membrane proteins of Actinobacillus actinomycetemcomitans.伴放线放线杆菌粗糙菌落特异性外膜蛋白的鉴定与分子分析
Infect Immun. 1999 Jun;67(6):2901-8. doi: 10.1128/IAI.67.6.2901-2908.1999.
9
Purification and characterization of a trypsin-like protease from the culture supernatant of Actinobacillus actinomycetemcomitans Y4.从伴放线放线杆菌Y4培养上清液中纯化和鉴定一种类胰蛋白酶蛋白酶
Eur J Oral Sci. 1999 Apr;107(2):147-53. doi: 10.1046/j.0909-8836.1999.eos107211.x.
10
Actinobacillus actinomycetemcomitans immunosuppressive protein is a member of the family of cytolethal distending toxins capable of causing a G2 arrest in human T cells.伴放线放线杆菌免疫抑制蛋白是细胞致死性膨胀毒素家族的成员之一,能够使人类T细胞停滞于G2期。
J Immunol. 1999 Apr 15;162(8):4773-80.

伴放线放线杆菌的非特异性黏附需要在细菌和古细菌中广泛存在的基因。

Nonspecific adherence by Actinobacillus actinomycetemcomitans requires genes widespread in bacteria and archaea.

作者信息

Kachlany S C, Planet P J, Bhattacharjee M K, Kollia E, DeSalle R, Fine D H, Figurski D H

机构信息

Department of Microbiology, College of Physicians and Surgeons, Columbia University, New York, New York 10032, USA.

出版信息

J Bacteriol. 2000 Nov;182(21):6169-76. doi: 10.1128/JB.182.21.6169-6176.2000.

DOI:10.1128/JB.182.21.6169-6176.2000
PMID:11029439
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC94753/
Abstract

The gram-negative coccobacillus, Actinobacillus actinomycetemcomitans, is the putative agent for localized juvenile periodontitis, a particularly destructive form of periodontal disease in adolescents. This bacterium has also been isolated from a variety of other infections, notably endocarditis. Fresh clinical isolates of A. actinomycetemcomitans form tenacious biofilms, a property likely to be critical for colonization of teeth and other surfaces. Here we report the identification of a locus of seven genes required for nonspecific adherence of A. actinomycetemcomitans to surfaces. The recently developed transposon IS903phikan was used to isolate mutants of the rough clinical isolate CU1000 that are defective in tight adherence to surfaces (Tad(-)). Unlike wild-type cells, Tad(-) mutant cells adhere poorly to surfaces, fail to form large autoaggregates, and lack long, bundled fibrils. Nucleotide sequencing and genetic complementation analysis revealed a 6.7-kb region of the genome with seven adjacent genes (tadABCDEFG) required for tight adherence. The predicted TadA polypeptide is similar to VirB11, an ATPase involved in macromolecular transport. The predicted amino acid sequences of the other Tad polypeptides indicate membrane localization but no obvious functions. We suggest that the tad genes are involved in secretion of factors required for tight adherence of A. actinomycetemcomitans. Remarkably, complete and highly conserved tad gene clusters are present in the genomes of the bubonic plague bacillus Yersinia pestis and the human and animal pathogen Pasteurella multocida. Partial tad loci also occur in strikingly diverse Bacteria and Archaea. Our results show that the tad genes are required for tight adherence of A. actinomycetemcomitans to surfaces and are therefore likely to be essential for colonization and pathogenesis. The occurrence of similar genes in a wide array of microorganisms indicates that they have important functions. We propose that tad-like genes have a significant role in microbial colonization.

摘要

革兰氏阴性球杆菌——伴放线放线杆菌,被认为是局限性青少年牙周炎的病原体,这是一种在青少年中具有特别破坏性的牙周疾病形式。这种细菌也已从多种其他感染中分离出来,尤其是心内膜炎。伴放线放线杆菌的新鲜临床分离株会形成坚韧的生物膜,这一特性可能对其在牙齿和其他表面的定殖至关重要。在此,我们报告了对伴放线放线杆菌非特异性黏附于表面所需的一个由七个基因组成的基因座的鉴定。最近开发的转座子IS903phikan被用于分离粗糙临床分离株CU1000的突变体,这些突变体在紧密黏附于表面方面存在缺陷(Tad(-))。与野生型细胞不同,Tad(-)突变体细胞对表面的黏附性很差,无法形成大的自聚集体,并且缺乏长的、成束的纤丝。核苷酸测序和基因互补分析揭示了基因组中一个6.7 kb的区域,其中有七个相邻基因(tadABCDEFG)是紧密黏附所必需的。预测的TadA多肽与VirB11相似,VirB11是一种参与大分子运输的ATP酶。其他Tad多肽的预测氨基酸序列表明它们定位于膜上,但没有明显功能。我们认为tad基因参与了伴放线放线杆菌紧密黏附所需因子的分泌。值得注意的是,在鼠疫杆菌耶尔森氏菌和人畜共患病原体多杀巴斯德氏菌的基因组中存在完整且高度保守的tad基因簇。部分tad基因座也存在于种类惊人的细菌和古细菌中。我们的结果表明,tad基因是伴放线放线杆菌紧密黏附于表面所必需的,因此可能对定殖和发病机制至关重要。在多种微生物中出现相似基因表明它们具有重要功能。我们提出,类tad基因在微生物定殖中具有重要作用。