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金黄色葡萄球菌对新型隐球菌的杀伤作用:隐球菌荚膜多糖在真菌-细菌相互作用中的作用

Killing of cryptococcus neoformans by Staphylococcus aureus: the role of cryptococcal capsular polysaccharide in the fungal-bacteria interaction.

作者信息

Saito Fumito, Ikeda Reiko

机构信息

Department of Microbiology, Meiji Pharmaceutical University, Kiyose, Tokyo, Japan.

出版信息

Med Mycol. 2005 Nov;43(7):603-12. doi: 10.1080/13693780500078417.

Abstract

Microbes compete for the environmental niche which is their host. To investigate the effects of a pathogenic bacterium on invasion and colonization by a pathogenic yeast, Cryptococcus neoformans was co-cultured with Staphylococcus aureus. We found that the number of colony forming units of C. neoformans was decreased by Staphylococcus aureus. In contrast, the viability of Candida albicans was not affected. Under the microscope, wild-type C. neoformans cells were shown to be surrounded by S. aureus, while cells of a capsuleless mutant of C. neoformans were not. C. neoformans was not killed when a membrane separated it from S. aureus in co-culture. Killing was confirmed by staining with cyanoditolyl tetrazolium chloride: S. aureus stained red, indicating viability, while C. neojormans did not stain, indicating lethality. The in situ terminal deoxynucleotidyl transferase-mediated dUTR nick end labeling (TUNEL) assay indicated cell death with fragmentation of DNA of C. neoformans. Capsular polysaccharide from C. neoformans inhibited the killing. Treatment of the crude polysaccharide with protease increased the inhibition. The protective activity resided in the glucuronoxylomannan (GXM) fraction, although the concentration required for the inhibition was high. These results suggest that S. aureus kills C. neoformans by a process that involves attachment to the cryptococcal capsule.

摘要

微生物会争夺作为其宿主的环境生态位。为了研究一种致病细菌对致病性酵母侵袭和定殖的影响,将新型隐球菌与金黄色葡萄球菌共同培养。我们发现金黄色葡萄球菌会使新型隐球菌的菌落形成单位数量减少。相比之下,白色念珠菌的活力未受影响。在显微镜下,野生型新型隐球菌细胞被金黄色葡萄球菌包围,而新型隐球菌无荚膜突变体的细胞则未被包围。在共培养中,当用膜将新型隐球菌与金黄色葡萄球菌隔开时,新型隐球菌不会被杀死。用氯化三苯基四氮唑染色证实了杀伤作用:金黄色葡萄球菌染成红色,表明有活力,而新型隐球菌未染色,表明已死亡。原位末端脱氧核苷酸转移酶介导的dUTP缺口末端标记(TUNEL)分析表明新型隐球菌的DNA片段化导致细胞死亡。新型隐球菌的荚膜多糖可抑制这种杀伤作用。用蛋白酶处理粗多糖可增强这种抑制作用。保护活性存在于葡糖醛酸木甘露聚糖(GXM)组分中,尽管抑制所需的浓度很高。这些结果表明,金黄色葡萄球菌通过一个涉及附着于隐球菌荚膜的过程杀死新型隐球菌。

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