Biais Nicolas, Ladoux Benoît, Higashi Dustin, So Magdalene, Sheetz Michael
Department of Biological Sciences, Columbia University, New York, New York, United States of America.
PLoS Biol. 2008 Apr 15;6(4):e87. doi: 10.1371/journal.pbio.0060087.
The causative agent of gonorrhea, Neisseria gonorrhoeae, bears retractable filamentous appendages called type IV pili (Tfp). Tfp are used by many pathogenic and nonpathogenic bacteria to carry out a number of vital functions, including DNA uptake, twitching motility (crawling over surfaces), and attachment to host cells. In N. gonorrhoeae, Tfp binding to epithelial cells and the mechanical forces associated with this binding stimulate signaling cascades and gene expression that enhance infection. Retraction of a single Tfp filament generates forces of 50-100 piconewtons, but nothing is known, thus far, on the retraction force ability of multiple Tfp filaments, even though each bacterium expresses multiple Tfp and multiple bacteria interact during infection. We designed a micropillar assay system to measure Tfp retraction forces. This system consists of an array of force sensors made of elastic pillars that allow quantification of retraction forces from adherent N. gonorrhoeae bacteria. Electron microscopy and fluorescence microscopy were used in combination with this novel assay to assess the structures of Tfp. We show that Tfp can form bundles, which contain up to 8-10 Tfp filaments, that act as coordinated retractable units with forces up to 10 times greater than single filament retraction forces. Furthermore, single filament retraction forces are transient, whereas bundled filaments produce retraction forces that can be sustained. Alterations of noncovalent protein-protein interactions between Tfp can inhibit both bundle formation and high-amplitude retraction forces. Retraction forces build over time through the recruitment and bundling of multiple Tfp that pull cooperatively to generate forces in the nanonewton range. We propose that Tfp retraction can be synchronized through bundling, that Tfp bundle retraction can generate forces in the nanonewton range in vivo, and that such high forces could affect infection.
淋病的病原体淋病奈瑟菌带有可收缩的丝状附属物,称为IV型菌毛(Tfp)。许多致病性和非致病性细菌利用Tfp来执行多种重要功能,包括摄取DNA、颤动运动(在表面爬行)以及附着于宿主细胞。在淋病奈瑟菌中,Tfp与上皮细胞的结合以及与此结合相关的机械力会刺激信号级联反应和基因表达,从而增强感染。单根Tfp细丝的收缩会产生50-100皮牛顿的力,但到目前为止,对于多根Tfp细丝的收缩力能力还一无所知,尽管每个细菌都表达多根Tfp,并且在感染过程中多个细菌会相互作用。我们设计了一种微柱测定系统来测量Tfp的收缩力。该系统由一系列由弹性柱制成的力传感器组成,可对附着的淋病奈瑟菌的收缩力进行量化。电子显微镜和荧光显微镜与这种新型测定方法结合使用,以评估Tfp的结构。我们发现Tfp可以形成束,其中包含多达8-10根Tfp细丝,这些束作为协调的可收缩单元,其产生的力比单根细丝的收缩力大10倍。此外,单根细丝的收缩力是短暂的,而束状细丝产生的收缩力可以持续。Tfp之间非共价蛋白质-蛋白质相互作用的改变会抑制束的形成和高幅度收缩力。收缩力会随着时间的推移通过多根Tfp的募集和成束而增强,这些Tfp协同拉动以产生纳牛顿范围内的力。我们提出,Tfp的收缩可以通过成束实现同步,Tfp束的收缩可以在体内产生纳牛顿范围内的力,并且如此高的力可能会影响感染。