Bryan R A, Zaragoza O, Zhang T, Ortiz G, Casadevall A, Dadachova E
Department of Nuclear Medicine, Albert Einstein College of Medicine, 1695A Eastchester Rd., Bronx, NY 10461, USA.
Eukaryot Cell. 2005 Feb;4(2):465-75. doi: 10.1128/EC.4.2.465-475.2005.
The polysaccharide capsule of the pathogenic fungus Cryptococcus neoformans is an important virulence factor, but relatively little is known about its architecture. We applied a combination of radiological, chemical, and serological methods to investigate the structure of this polysaccharide capsule. Exposure of C. neoformans cells to gamma radiation, dimethyl sulfoxide, or radiolabeled monoclonal antibody removed a significant part of the capsule. Short intervals of gamma irradiation removed the outer portion of the cryptococcal capsule without killing cells, which could subsequently repair their capsules. Survival analysis of irradiated wild-type, acapsular mutant, and complemented mutant strains demonstrated that the capsule contributed to radioprotection and had a linear attenuation coefficient higher than that of lead. The capsule portions remaining after dimethyl sulfoxide or gamma radiation treatment were comparable in size, 65 to 66 microm3, and retained immunoreactivity for a monoclonal antibody to glucuronoxylomannan. Simultaneous or sequential treatment of the cells with dimethyl sulfoxide and radiation removed the remaining capsule so that it was not visible by light microscopy. The capsule could be protected against radiation by either of the free radical scavengers ascorbic acid and sorbitol. Sugar composition analysis of polysaccharide removed from the outer and inner parts of the capsule revealed significant differences in glucuronic acid and xylose molar ratios, implying differences in the chemical structure of the constituent polysaccharides. Our results provide compelling evidence for the existence of two zones in the C. neoformans capsule that differ in susceptibility to dimethyl sulfoxide and radiation and, possibly, in packing and composition.
致病真菌新型隐球菌的多糖荚膜是一种重要的毒力因子,但其结构却鲜为人知。我们应用放射学、化学和血清学方法相结合来研究这种多糖荚膜的结构。将新型隐球菌细胞暴露于γ射线、二甲基亚砜或放射性标记的单克隆抗体下会去除荚膜的很大一部分。短时间的γ射线照射会去除隐球菌荚膜的外层部分而不杀死细胞,这些细胞随后能够修复它们的荚膜。对经照射的野生型、无荚膜突变体和互补突变体菌株的存活分析表明,荚膜有助于辐射防护,并且其线性衰减系数高于铅。经二甲基亚砜或γ射线处理后剩余的荚膜部分大小相当,为65至66立方微米,并且保留了对葡糖醛酸木甘露聚糖单克隆抗体的免疫反应性。用二甲基亚砜和辐射同时或先后处理细胞会去除剩余的荚膜,以至于在光学显微镜下不可见。荚膜可以被自由基清除剂抗坏血酸和山梨醇中的任何一种保护免受辐射。对从荚膜外层和内层去除的多糖进行糖组成分析发现,葡糖醛酸和木糖的摩尔比存在显著差异,这意味着组成多糖的化学结构存在差异。我们的结果为新型隐球菌荚膜中存在两个对二甲基亚砜和辐射敏感性不同、可能在堆积和组成方面也不同的区域提供了有力证据。