DeAngelis P L, Weigel P H
Department of Human Biological Chemistry and Genetics, University of Texas Medical Branch, Galveston, Texas, USA 77555-0647.
Diagn Microbiol Infect Dis. 1994 Oct;20(2):77-80. doi: 10.1016/0732-8893(94)90095-7.
One of the virulence factors of group A streptococci is the hyaluronic acid polysaccharide capsule. A rapid method for ascertaining the status of the capsule phenotype in Streptococcus pyogenes is described. Bacteria with a capsule have a lower buoyant density than acapsular or hyaluronidase-treated cells. Early log phase cultures were underlaid with 65% Percoll and centrifuged at 500-1000 g for 5 min. Upon visual examination, encapsulated cells were observed at the interface, whereas acapsular cells appeared in the pellet. Cultures that produced at least 7 micrograms/ml of hyaluronic acid per A600 unit of cells were detected at the interface; this level of polysaccharide is only about 0.5%-4% of that found for most mucoid strains. Therefore, this procedure can detect capsules around strains that do not appear to be encapsulated by light microscopy or do not possess mucoid colony morphology. Furthermore, this method reduces dependence on other expensive assays that use labile radioactive reagents to detect hyaluronic acid.
A群链球菌的毒力因子之一是透明质酸多糖荚膜。本文描述了一种快速确定化脓性链球菌荚膜表型状态的方法。有荚膜的细菌比无荚膜或经透明质酸酶处理的细胞具有更低的浮力密度。对数早期培养物用65%的 Percoll覆盖,并在500 - 1000 g下离心5分钟。通过肉眼检查,在界面处观察到有荚膜的细胞,而无荚膜的细胞出现在沉淀中。每A600单位细胞产生至少7微克/毫升透明质酸的培养物在界面处被检测到;这个多糖水平仅约为大多数黏液样菌株所发现水平的0.5% - 4%。因此,该程序可以检测到在光学显微镜下似乎没有被包裹或不具有黏液样菌落形态的菌株周围的荚膜。此外,该方法减少了对其他使用不稳定放射性试剂来检测透明质酸的昂贵检测方法的依赖。