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利用差异显示逆转录聚合酶链反应鉴定牙龈卟啉单胞菌在人牙龈上皮细胞中特异性表达的基因。

Identification of Porphyromonas gingivalis genes specifically expressed in human gingival epithelial cells by using differential display reverse transcription-PCR.

作者信息

Park Yoonsuk, Yilmaz Ozlem, Jung Il-Young, Lamont Richard J

机构信息

Department of Oral Biology, College of Dentistry, University of Florida, Gainesville, FL 32610, USA.

出版信息

Infect Immun. 2004 Jul;72(7):3752-8. doi: 10.1128/IAI.72.7.3752-3758.2004.

Abstract

Porphyromonas gingivalis, one of the causative agents of adult periodontitis, can invade and survive within host epithelial cells. The molecular mechanisms by which P. gingivalis induces uptake and adapts to an intracellular environment are not fully understood. In this study, we have investigated the genetic responses of P. gingivalis internalized within human gingival epithelial cells (GECs) in order to identify factors involved in invasion and survival. We compared the differential display of arbitrarily PCR-amplified gene transcripts in P. gingivalis recovered from GECs with the display of transcripts in P. gingivalis control cultures. Over 20 potential differentially expressed transcripts were identified. Among these, pepO, encoding an endopeptidase, and genes encoding an ATP-binding cassette (ABC) transporter and a cation-transporting ATPase were upregulated in GECs. To investigate the functionality of these gene products, mutants were generated by insertional inactivation. Compared to the parental strain, mutants of each gene showed a significant reduction in their invasion capabilities. In addition, GEC cytoskeletal responses to the mutants were distinct from those induced by the parent. In contrast, adhesion of the mutant strains to GECs was not affected by lack of expression of the gene products. These results suggest that PepO, a cation-transporting ATPase, and an ABC transporter are required for the intracellular lifestyle of P. gingivalis.

摘要

牙龈卟啉单胞菌是成人牙周炎的病原体之一,可侵入宿主上皮细胞并在其中存活。牙龈卟啉单胞菌诱导摄取并适应细胞内环境的分子机制尚未完全了解。在本研究中,我们调查了内化于人类牙龈上皮细胞(GECs)中的牙龈卟啉单胞菌的基因反应,以确定参与侵袭和存活的因素。我们将从GECs中回收的牙龈卟啉单胞菌中任意PCR扩增的基因转录本的差异显示与牙龈卟啉单胞菌对照培养物中转录本的显示进行了比较。鉴定出20多个潜在的差异表达转录本。其中,编码内肽酶的pepO以及编码ATP结合盒(ABC)转运蛋白和阳离子转运ATP酶的基因在GECs中上调。为了研究这些基因产物的功能,通过插入失活产生了突变体。与亲本菌株相比,每个基因的突变体在侵袭能力上均显著降低。此外,GEC对突变体的细胞骨架反应与亲本诱导的反应不同。相反,突变菌株对GECs的粘附不受基因产物表达缺失的影响。这些结果表明,PepO、阳离子转运ATP酶和ABC转运蛋白是牙龈卟啉单胞菌细胞内生存方式所必需的。

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