Department of Microbiology, Immunology, and Cell Biology, West Virginia University Health Sciences Center, Morgantown, WV 26506-9177, USA.
Laboratory of Intracellular Parasites, NIAID, Rocky Mountain Laboratories, Hamilton, MT 59840, USA.
Microbiology (Reading). 2010 Feb;156(Pt 2):356-373. doi: 10.1099/mic.0.033241-0. Epub 2009 Nov 12.
Type III secretion (T3S) functions in establishing infections in a large number of Gram-negative bacteria, yet little is known about how host cell properties might function in this process. We used the opportunistic pathogen Pseudomonas aeruginosa and the ability to alter host cell sensitivity to Pseudomonas T3S to explore this problem. HT-29 epithelial cells were used to study cellular changes associated with loss of T3S sensitivity, which could be induced by treatment with methyl-beta-cyclodextrin or perfringolysin O. HL-60 promyelocytic cells are innately resistant to Pseudomonas T3S and were used to study cellular changes occurring in response to induction of T3S sensitivity, which occurred following treatment with phorbol esters. Using both cell models, a positive correlation was observed between eukaryotic cell adherence to tissue culture wells and T3S sensitivity. In examining the type of adhesion process linked to T3S sensitivity in HT-29 cells, a hierarchical order of protein involvement was identified that paralleled the architecture of leading edge (LE) focal complexes. Conversely, in HL-60 cells, induction of T3S sensitivity coincided with the onset of LE properties and the development of actin-rich projections associated with polarized cell migration. When LE architecture was examined by immunofluorescent staining for actin, Rac1, IQ-motif-containing GTPase-activating protein 1 (IQGAP1) and phosphatidylinositol 3 kinase (PI3 kinase), intact LE structure was found to closely correlate with host cell sensitivity to P. aeruginosa T3S. Our model for host cell involvement in Pseudomonas T3S proposes that cortical actin polymerization at the LE alters membrane properties to favour T3S translocon function and the establishment of infections, which is consistent with Pseudomonas infections targeting wounded epithelial barriers undergoing cell migration.
III 型分泌系统(T3S)在许多革兰氏阴性菌的感染建立中发挥作用,但宿主细胞特性如何在这一过程中发挥作用知之甚少。我们利用机会性病原体铜绿假单胞菌和改变宿主细胞对铜绿假单胞菌 T3S 敏感性的能力来探索这个问题。HT-29 上皮细胞用于研究与 T3S 敏感性丧失相关的细胞变化,这些变化可以通过用甲基-β-环糊精或产气荚膜梭菌α毒素处理来诱导。HL-60 早幼粒细胞对铜绿假单胞菌 T3S 天然具有抗性,并用于研究在诱导 T3S 敏感性时发生的细胞变化,这种变化发生在用佛波醇酯处理后。使用这两种细胞模型,观察到真核细胞对组织培养孔的黏附与 T3S 敏感性之间存在正相关。在检查与 HT-29 细胞 T3S 敏感性相关的粘附过程的类型时,确定了一种蛋白质参与的层次顺序,该顺序与前沿(LE)焦点复合物的结构相平行。相反,在 HL-60 细胞中,T3S 敏感性的诱导与 LE 特性的出现以及与极化细胞迁移相关的富含肌动蛋白的突起的发展相吻合。当通过免疫荧光染色用肌动蛋白、Rac1、含有 IQ 基序的 GTP 酶激活蛋白 1(IQGAP1)和磷酸肌醇 3 激酶(PI3 激酶)检查 LE 结构时,发现完整的 LE 结构与宿主细胞对铜绿假单胞菌 T3S 的敏感性密切相关。我们提出的宿主细胞参与铜绿假单胞菌 T3S 的模型表明,LE 处皮质肌动蛋白的聚合改变了膜特性,有利于 T3S 转位器的功能和感染的建立,这与铜绿假单胞菌感染靶向正在进行细胞迁移的受伤上皮屏障是一致的。