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牙龈卟啉单胞菌的毒力因子与对心血管系统细胞的侵袭

Porphyromonas gingivalis virulence factors and invasion of cells of the cardiovascular system.

作者信息

Progulske-Fox A, Kozarov E, Dorn B, Dunn W, Burks J, Wu Y

机构信息

University of Florida, Department of Oral Biology, Gainesville 32606, USA.

出版信息

J Periodontal Res. 1999 Oct;34(7):393-9. doi: 10.1111/j.1600-0765.1999.tb02272.x.

Abstract

Our laboratory is interested in the genes and gene products involved in the interactions between Porphyromonas gingivalis (Pg) and the host. These interactions may occur in either the periodontal tissues or other non-oral host tissues such as those of the cardiovascular system. We have previously reported the cloning of several genes encoding hemagglutinins, surface proteins that interact with the host tissues, and are investigating their roles in the disease process. Primary among these is HagA, a very large protein with multiple functional groups that have significant sequence homology to protease genes of this species. Preliminary evidence indicates that an avirulent Salmonella typhimurium strain containing hagA is virulent in mice. These data indicate that HagA may be a key virulence factor of Pg. Additionally, we are investigating the invasion of primary human coronary artery endothelial cells (HCAEC) by Pg because of the recent epidemiological studies indicating a correlation between periodontal disease (PD) and coronary heart disease (CHD). We found that some, but not all, strains of Pg are able to invade these cells. Scanning electron microsopy of the infected HCAEC demonstrated that the invading organisms initially attached to the host cell surface as aggregates and by a "pedestal"-like structure. By transmission electronmicroscopy it could be seen that internalized bacteria were present within multimembranous compartments localized with rough endoplasmic reticulum. In addition, invasion of the HCAEC by Pg resulted in an increase in the degradation of long-lived cellular proteins. These data indicate that Pg are present within autophagosomes and may use components of the autophagic pathway as a means to survive intracellularly. However, Pg presence within autophagosomes in KB cells could not be observed or detected. It is therefore likely that Pg uses different invasive mechanisms for different host cells. This and the role of HagA in invasion is currently being investigated further.

摘要

我们实验室关注参与牙龈卟啉单胞菌(Pg)与宿主相互作用的基因及基因产物。这些相互作用可能发生在牙周组织或其他非口腔宿主组织,如心血管系统组织中。我们之前报道过克隆几个编码血凝素的基因,血凝素是与宿主组织相互作用的表面蛋白,并且正在研究它们在疾病过程中的作用。其中主要的是HagA,它是一种非常大的蛋白质,具有多个功能基团,与该物种的蛋白酶基因有显著的序列同源性。初步证据表明,含有hagA的无毒鼠伤寒沙门氏菌菌株在小鼠中具有毒性。这些数据表明HagA可能是Pg的关键毒力因子。此外,由于最近的流行病学研究表明牙周病(PD)与冠心病(CHD)之间存在关联,我们正在研究Pg对原代人冠状动脉内皮细胞(HCAEC)的侵袭。我们发现,部分(而非全部)Pg菌株能够侵袭这些细胞。对感染的HCAEC进行扫描电子显微镜观察表明,入侵的生物体最初以聚集体形式并通过“基座”样结构附着于宿主细胞表面。通过透射电子显微镜可以看到,内化的细菌存在于与粗面内质网定位在一起的多膜隔室内。此外,Pg对HCAEC的侵袭导致长寿命细胞蛋白的降解增加。这些数据表明Pg存在于自噬体中,并且可能利用自噬途径的成分作为细胞内存活的一种方式。然而,在KB细胞中未观察到或检测到Pg存在于自噬体中。因此,Pg很可能对不同的宿主细胞使用不同的侵袭机制。目前正在进一步研究这一点以及HagA在侵袭中的作用。

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