Nickel J C, Olson M, McLean R J, Grant S K, Costerton J W
Br J Urol. 1987 Jan;59(1):21-30. doi: 10.1111/j.1464-410x.1987.tb04573.x.
Direct molecular and morphological techniques of modern microbiology were used to monitor the sequential development of bacterial microcolonies and biofilms in a rat model of urinary infection and to demonstrate that the urease activity of the infecting organisms sets in course a series of reactions in which struvite and apatite crystals develop within the matrix of the enlarging bacterial aggregate. This forms multiple stone nidi on the uroepithelial surface upon which succeeding bacterial biofilms develop and with the incorporation of other urine components, such as urinary mucroproteins, establishes a matrix skeleton that becomes mineralised, thus allowing for the growth of the stone in concentric layers. To arrive at this hypothesis, we studied infection stone genesis using a newly developed model for infection-induced bladder stone formation in the rat. We examined in detail the sequential events in the evolving microbial ecology of progressive struvite calculogenesis, using conventional microbiological techniques, direct ultrastructural observation, newly developed ultrastructural cytochemical localisation techniques and immunological procedures for stabilisation of the biofilm glycocalix and stone matrix in the rat model. It was concluded that the organic glycocalix material secreted by the associated bacteria comprises a substantial and aetiologically important part of the infection stone calculogenesis and matrix production.
现代微生物学的直接分子和形态学技术被用于监测大鼠尿路感染模型中细菌微菌落和生物膜的连续发育,并证明感染微生物的脲酶活性引发了一系列反应,在此过程中鸟粪石和磷灰石晶体在不断扩大的细菌聚集体基质中形成。这在尿上皮表面形成多个结石核心,后续的细菌生物膜在其上发育,并随着其他尿液成分(如尿粘蛋白)的掺入,形成一个矿化的基质骨架,从而使结石能够以同心层的形式生长。为了得出这一假设,我们使用一种新开发的大鼠感染性膀胱结石形成模型研究了感染性结石的成因。我们使用传统微生物技术、直接超微结构观察、新开发的超微结构细胞化学定位技术以及用于稳定大鼠模型中生物膜糖萼和结石基质的免疫学方法,详细研究了进行性鸟粪石结石形成过程中不断演变的微生物生态中的连续事件。得出的结论是,相关细菌分泌的有机糖萼物质在感染性结石形成和基质产生中占很大比例且在病因学上具有重要意义。