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一种海洋微藻(多边舌甲藻)硫酸化多糖对人类免疫缺陷病毒及其他包膜病毒的体外抗病毒活性

In vitro antiviral activities of sulfated polysaccharides from a marine microalga (Cochlodinium polykrikoides) against human immunodeficiency virus and other enveloped viruses.

作者信息

Hasui M, Matsuda M, Okutani K, Shigeta S

机构信息

Faculty of Agriculture, Kagawa University, Japan.

出版信息

Int J Biol Macromol. 1995 Oct;17(5):293-7. doi: 10.1016/0141-8130(95)98157-t.

Abstract

A marine microalga, Cochlodinium polykrikoides, produces extracellular sulfated polysaccharides. Isolation and purification of the polysaccharides were accomplished by precipitation with ethanol and Cetavlon, followed by DEAE-cellulose column chromatography (polysaccharides A1 and A2). These polysaccharides, which were homogeneous when analysed by both ultracentrifugal and electrophoretic methods, were composed of mannose, galactose, glucose and uronic acid, together with sulfate groups (S = 7-8% w/w). Both A1 and A2 inhibited the cytopathic effect of influenza virus types A and B in MDCK cells, that of respiratory syncytial virus types A and B in HEp-2 cells, that of human immunodeficiency virus type 1 in MT-4 cells; and, except A1 for herpes simplex virus type 1 and A2 for parainfluenza virus type 2 in HMV-2 cells, the cochlodinium polysaccharides showed no antiviral activity against parainfluenza virus types 2 and 3, measles virus, mumps virus or herpes simplex virus type 1 in HMV-2 cells. No cytotoxicity for host cells was observed with these polysaccharides at a concentration of 100 micrograms ml-1. Inhibitory effects on various viruses were achieved at concentrations that were not markedly inhibitory to the blood coagulation process.

摘要

一种海洋微藻,多环旋沟藻(Cochlodinium polykrikoides),能产生细胞外硫酸化多糖。通过用乙醇和十六烷基三甲基溴化铵沉淀,随后进行DEAE - 纤维素柱色谱法(多糖A1和A2),完成了多糖的分离和纯化。这些多糖通过超速离心和电泳方法分析时是均一的,由甘露糖、半乳糖、葡萄糖和糖醛酸以及硫酸基团组成(S = 7 - 8% w/w)。A1和A2均能抑制甲型和乙型流感病毒在MDCK细胞中的细胞病变效应、甲型和乙型呼吸道合胞病毒在HEp - 2细胞中的细胞病变效应、1型人类免疫缺陷病毒在MT - 4细胞中的细胞病变效应;并且,除了A1对单纯疱疹病毒1型和A2对副流感病毒2型在HMV - 2细胞中无抗病毒活性外,多环旋沟藻多糖对HMV - 2细胞中的副流感病毒2型和3型、麻疹病毒、腮腺炎病毒或单纯疱疹病毒1型均无抗病毒活性。在100微克/毫升的浓度下,这些多糖对宿主细胞未观察到细胞毒性。在对血液凝固过程无明显抑制作用的浓度下实现了对各种病毒的抑制作用。

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