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淋球菌从极化上皮细胞的顶端和基底离开,并在IV型菌毛中表现出动态变化。

Gonococci exit apically and basally from polarized epithelial cells and exhibit dynamic changes in type IV pili.

作者信息

Criss Alison K, Seifert H Steven

机构信息

Department of Microbiology-Immunology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.

出版信息

Cell Microbiol. 2006 Sep;8(9):1430-43. doi: 10.1111/j.1462-5822.2006.00722.x.

Abstract

Type IV pili are a major virulence factor of the obligate human pathogen Neisseria gonorrhoeae (the gonococcus; Gc). Pili facilitate bacterial adherence to epithelial cells, but their participation in later steps of epithelial infection, particularly intracellular replication and exit, is poorly understood. Using polarized T84 cells as a model for mature mucosal epithelia, pilus dynamics in piliated, Opa-expressing Gc were examined over time. T84 infection was characterized by a several-hour delay in the growth of cell-associated bacteria and by non-directional exit of Gc, the first time these phenomena have been reported. During infection, non-piliated progeny arose stochastically from piliated progenitors. Piliated and non-piliated Gc replicated and exited from T84 cell monolayers equally well, demonstrating that piliation did not influence Gc survival during epithelial infection. The frequency with which pilin variants arose from a defined piliated progenitor during T84 cell infection was found to be sufficiently high to account for the extensive pilin variation reported during human infection. However, the repertoire of variants appearing in association with T84 cells was similar to what was seen in the absence of cells, demonstrating that polarized epithelial cells can support Gc replication without selecting for a subset of pilin variants or piliation states.

摘要

IV型菌毛是人类专性病原体淋病奈瑟菌(淋球菌;Gc)的主要毒力因子。菌毛有助于细菌黏附上皮细胞,但它们在上皮感染后期步骤中的参与情况,尤其是细胞内复制和穿出,目前了解甚少。使用极化的T84细胞作为成熟黏膜上皮的模型,对表达菌毛、Opa的Gc中的菌毛动力学随时间进行了研究。T84感染的特征是与细胞相关的细菌生长延迟数小时,以及Gc的非定向穿出,这些现象首次被报道。在感染过程中,无菌毛后代随机地从有菌毛祖细胞产生。有菌毛和无菌毛的Gc在T84细胞单层中同样能够很好地复制和穿出,这表明菌毛化在上皮感染期间不影响Gc的存活。发现在T84细胞感染期间,从特定有菌毛祖细胞产生菌毛蛋白变体的频率足够高,足以解释在人类感染期间报道的广泛菌毛蛋白变异。然而,与T84细胞相关出现的变体库与在无细胞情况下所见相似,这表明极化上皮细胞可以支持Gc复制,而无需选择菌毛蛋白变体或菌毛化状态的一个子集。

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