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The study of adhesive forces between the type 3 fimbriae of Klebsiella pneumoniae and collagen-coated surfaces by using laser tweezers

机译:用激光镊子研究肺炎克雷伯菌3型菌毛与胶原蛋白包被表面之间的粘附力

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Adherence to host cells by a bacterial pathogen is a critical step for establishment of infection. It will contribute greatly to the understanding of bacterial pathogenesis by studying the biological force between a single pair of pathogen and host cell. In our experiment, we use a calibrated optical tweezers system to detach a single Klebsiella pneumoniae, the pathogen, from collagen, the host. By gradually increasing the laser power of the optical tweezers until the Klebsiella pneumoniae is detached from the collagen, we obtain the magnitude of the adhesive force between them. This happens when the adhesive force is barely equal to the trapping force provided by the optical tweezers at that specific laser power. This study is important because Klebsiella pneumoniae is an opportunistic pathogen which causes suppurative lesions, urinary and respiratory tract infections. It has been proved that type 3 fimbrial adhesin (mrkD) is strongly associated with the adherence of Klebsiella pneumoniae. Besides, four polymorphic mrkD alleles: namely, mrkDv1, v2, v3, and v4, are typed by using RFLP. In order to investigate the relationship between the structure and the function for each of these variants, DNA fragments encoding the major fimbrial proteins mrkA, mrkB, mrkC are expressed together with any of the four mrkD adhesins in E. coli JM109. Our study shows that the E. coli strain carrying the mrkDv3 fimbriae has the strongest binding activity. This suggests that mrkDv3 is a key factor that enhances the adherence of Klebsiella Pneumoniae to human body.
机译:细菌病原体对宿主细胞的粘附是建立感染的关键步骤。通过研究单对病原体与宿主细胞之间的生物学作用,它将为理解细菌的发病机理做出巨大贡献。在我们的实验中,我们使用校准的光学镊子系统从胶原蛋白宿主中分离出一种病原体肺炎克雷伯菌。通过逐渐增加光镊的激光功率,直到肺炎克雷伯菌与胶原蛋白脱离,我们获得了它们之间的粘附力大小。当粘合力几乎等于光镊在该特定激光功率下提供的捕获力时,就会发生这种情况。这项研究很重要,因为肺炎克雷伯菌是一种机会性病原体,可引起化脓性病变,泌尿和呼吸道感染。业已证明,3型纤维粘附素(mrkD)与肺炎克雷伯菌的粘附密切相关。此外,使用RFLP输入了四个多态性mrkD等位基因:mrkDv1,v2,v3和v4。为了研究这些变体中每一个的结构与功能之间的关系,在大肠杆菌JM109中将编码主要纤维蛋白mrkA,mrkB,mrkC的DNA片段与四种mrkD粘附素中的任何一种一起表达。我们的研究表明,带有mrkDv3菌毛的大肠杆菌菌株具有最强的结合活性。这表明mrkDv3是增强肺炎克雷伯菌对人体粘附的关键因素。

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