Animal Research Institute, Murdoch University, Murdoch, Australia.
PLoS One. 2009 Dec 17;4(12):e8352. doi: 10.1371/journal.pone.0008352.
Brachyspira pilosicoli is an anaerobic spirochete that has received relatively little study, partly due to its specialized culture requirements and slow growth. This bacterium colonizes the large intestine of various species, including humans; typically, a dense layer of spirochete cells may be found intimately attached by one cell end to the surface of colonic enterocytes. Colonized individuals may develop colitis, but the mechanisms involved are not understood. The current study aimed to develop an in vitro model to investigate this process.
METHODOLOGY/PRINCIPAL FINDINGS: Four strains of B. pilosicoli were incubated at a high multiplicity of infection with monolayers of a human colonic adenocarcinoma cell line (Caco-2 cells). One strain isolated from a pig (95/1000) and one from a human (WesB) attached to the monolayers. Colonization increased with time, with the Caco-2 cell junctions being the initial targets of attachment. By electron microscopy, individual spirochete cells could be seen to have one cell end invaginated into the Caco-2 cell membranes, with the rest of the spirochete draped over the Caco-2 cell surface. After 6 h incubation, the monolayer was covered with a layer of spirochetes. Colonized monolayers demonstrated a time-dependent series of changes: staining with labelled phalloidin identified accumulation of actin at the cell junctions; ZO-1 staining revealed a loss of Caco-2 tight junction integrity; and Hoechst staining showed condensation and fragmentation of nuclear material consistent with apoptosis. Using quantitative reverse transcription PCR, the colonized monolayers demonstrated a significant up-regulation of interleukin-1beta (IL-1beta) and IL-8 expression. B. pilosicoli sonicates caused significant up-regulation of IL-1beta, TNF-alpha, and IL-6, but culture supernatants and non-pathogenic Brachyspira innocens did not alter cytokine expression.
CONCLUSIONS/SIGNIFICANCE: The changes induced in the Caco-2 cells provide evidence that B. pilosicoli has pathogenic potential, and give insights into the likely in vivo pathogenesis.
短螺旋体(Brachyspira pilosicoli)是一种厌氧螺旋体,由于其特殊的培养要求和缓慢的生长速度,研究相对较少。这种细菌定植于各种物种的大肠,包括人类;通常,密集的一层螺旋体细胞可能紧密地附着在结肠上皮细胞的表面。定植的个体可能会发展为结肠炎,但涉及的机制尚不清楚。本研究旨在建立体外模型来研究这一过程。
方法/主要发现: 将 4 株短螺旋体以高感染复数与单层人结肠腺癌细胞系(Caco-2 细胞)孵育。一株从猪中分离的菌株(95/1000)和一株从人分离的菌株(WesB)附着在单层上。随着时间的推移,定植增加,Caco-2 细胞连接处是附着的初始靶点。通过电子显微镜,可以看到单个螺旋体细胞的一端向内陷到 Caco-2 细胞膜中,其余的螺旋体则覆盖在 Caco-2 细胞表面。孵育 6 小时后,单层表面覆盖着一层螺旋体。定植的单层显示出一系列时间依赖性变化:用标记的鬼笔环肽染色鉴定细胞连接处肌动蛋白的积累;ZO-1 染色显示 Caco-2 紧密连接完整性丧失;Hoechst 染色显示核物质的凝聚和片段化,符合细胞凋亡的特征。使用定量逆转录 PCR,发现被定植的单层细胞中白细胞介素-1β(IL-1β)和 IL-8 的表达显著上调。短螺旋体超声裂解物导致 IL-1β、TNF-α和 IL-6 的显著上调,但培养上清液和非致病性无害短螺旋体(Brachyspira innocens)不会改变细胞因子的表达。
结论/意义: Caco-2 细胞发生的变化证明短螺旋体具有致病潜能,并深入了解可能的体内发病机制。