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通过消减杂交鉴定牙龈卟啉单胞菌强毒株特有的新型插入序列。

Identification by subtractive hybridization of a novel insertion sequence specific for virulent strains of Porphyromonas gingivalis.

作者信息

Sawada K, Kokeguchi S, Hongyo H, Sawada S, Miyamoto M, Maeda H, Nishimura F, Takashiba S, Murayama Y

机构信息

Department of Periodontology, Okayama University Dental School, Okayama 700-8525, Japan.

出版信息

Infect Immun. 1999 Nov;67(11):5621-5. doi: 10.1128/IAI.67.11.5621-5625.1999.

Abstract

Subtractive hybridization was employed to isolate specific genes from virulent Porphyromonas gingivalis strains that are possibly related to abscess formation. The genomic DNA from the virulent strain P. gingivalis W83 was subtracted with DNA from the avirulent strain ATCC 33277. Three clones unique to strain W83 were isolated and sequenced. The cloned DNA fragments were 885, 369, and 132 bp and had slight homology with only Bacillus stearothermophilus IS5377, which is a putative transposase. The regions flanking the cloned DNA fragments were isolated and sequenced, and the gene structure around the clones was revealed. These three clones were located side-by-side in a gene reported as an outer membrane protein. The three clones interrupt the open reading frame of the outer membrane protein gene. This inserted DNA, consisting of three isolated clones, was designated IS1598, which was 1,396 bp (i.e., a 1,158-bp open reading frame) in length and was flanked by 16-bp terminal inverted repeats and a 9-bp duplicated target sequence. IS1598 was detected in P. gingivalis W83, W50, and FDC 381 by Southern hybridization. All three P. gingivalis strains have been shown to possess abscess-forming ability in animal models. However, IS1598 was not detected in avirulent strains of P. gingivalis, including ATCC 33277. The IS1598 may interrupt the synthesis of the outer membrane protein, resulting in changes in the structure of the bacterial outer membrane. The IS1598 isolated in this study is a novel insertion element which might be a specific marker for virulent P. gingivalis strains.

摘要

采用消减杂交技术从具有毒力的牙龈卟啉单胞菌菌株中分离可能与脓肿形成相关的特定基因。用无毒菌株ATCC 33277的DNA对有毒菌株牙龈卟啉单胞菌W83的基因组DNA进行消减。分离并测序了W83菌株特有的三个克隆。克隆的DNA片段分别为885、369和132 bp,仅与嗜热脂肪芽孢杆菌IS5377(一种假定的转座酶)有轻微同源性。分离并测序了克隆DNA片段两侧的区域,揭示了克隆周围的基因结构。这三个克隆在一个被报道为外膜蛋白的基因中并排定位。这三个克隆中断了外膜蛋白基因的开放阅读框。由三个分离克隆组成的这种插入DNA被命名为IS1598,其长度为1396 bp(即1158 bp的开放阅读框),两侧是16 bp的末端反向重复序列和9 bp的重复靶序列。通过Southern杂交在牙龈卟啉单胞菌W83、W50和FDC 381中检测到IS1598。在动物模型中,所有这三种牙龈卟啉单胞菌菌株均已显示具有脓肿形成能力。然而在包括ATCC 33277在内的牙龈卟啉单胞菌无毒菌株中未检测到IS1598。IS1598可能会中断外膜蛋白的合成,导致细菌外膜结构发生变化。本研究中分离的IS1598是一种新型插入元件,可能是有毒牙龈卟啉单胞菌菌株的特异性标志物。

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