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宿主凝集素与致病性酵母新型隐球菌的结合:人表面活性蛋白D作为无荚膜酵母细胞的凝集素。

Binding of host collectins to the pathogenic yeast Cryptococcus neoformans: human surfactant protein D acts as an agglutinin for acapsular yeast cells.

作者信息

Schelenz S, Malhotra R, Sim R B, Holmskov U, Bancroft G J

机构信息

Department of Clinical Sciences, London School of Hygiene and Tropical Medicine, United Kingdom.

出版信息

Infect Immun. 1995 Sep;63(9):3360-6. doi: 10.1128/iai.63.9.3360-3366.1995.

Abstract

Cryptococcus neoformans is an opportunistic pathogen in AIDS patients causing disseminated disease and lethal meningitis after inhalation of acapsular or sparsely encapsulated yeast cells. In this study we have investigated whether a recently described family of primitive opsonins, termed collectins, contribute to innate resistance against C. neoformans. The pulmonary surfactant proteins SP-A and SP-D as well as the serum collectins mannose-binding protein and CL-43 bound in a calcium-dependent manner to acapsular C. neoformans in vitro. Binding was concentration dependent and abolished by competition with defined mono- and oligosaccharides. In contrast, no binding of the collectins was observed with the encapsulated form of the yeast. Furthermore, binding of purified collectin SP-D, but not SP-A, mannose-binding protein, or CL-43, led to a concentration-dependent agglutination of acapsular C. neoformans. These data indicate that collectins recognize carbohydrate structures in the cell wall of an initial infectious form of C. neoformans and may play a role in early antifungal defenses in the lung.

摘要

新型隐球菌是艾滋病患者的一种机会性致病病原体,吸入无荚膜或荚膜稀疏的酵母细胞后可引发播散性疾病和致命性脑膜炎。在本研究中,我们调查了最近描述的一类原始调理素(称为凝集素)是否有助于对新型隐球菌的天然抵抗。肺表面活性物质蛋白SP-A和SP-D以及血清凝集素甘露糖结合蛋白和CL-43在体外以钙依赖方式与无荚膜新型隐球菌结合。结合呈浓度依赖性,并可被特定单糖和寡糖的竞争所消除。相比之下,未观察到凝集素与酵母的荚膜形式结合。此外,纯化的凝集素SP-D(而非SP-A、甘露糖结合蛋白或CL-43)的结合导致无荚膜新型隐球菌发生浓度依赖性凝集。这些数据表明,凝集素识别新型隐球菌初始感染形式细胞壁中的碳水化合物结构,并可能在肺部早期抗真菌防御中发挥作用。

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本文引用的文献

1
Cryptococcus neoformans IV. The Not-So-Encapsulated Yeast.新型隐球菌 IV. 非包裹酵母菌。
Infect Immun. 1970 Jun;1(6):526-31. doi: 10.1128/iai.1.6.526-531.1970.
10

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