Hallak L K, Collins P L, Knudson W, Peeples M E
Immunology/Microbiology, Biochemistry and Pathology, Rush-Presbyterian-St. Luke's Medical Center, Chicago, IL 60612, USA.
Virology. 2000 Jun 5;271(2):264-75. doi: 10.1006/viro.2000.0293.
Respiratory syncytial virus (RSV) is an important human respiratory pathogen, particularly in infants. Glycosaminoglycans (GAGs) have been implicated in the initiation of RSV infection of cultured cells, but it is not clear what type of GAGs and GAG components are involved, whether the important GAGs are on the virus or the cell, or what the magnitude is of their contribution to infection. We constructed and rescued a recombinant green fluorescent protein (GFP)-expressing RSV (rgRSV) and used this virus to develop a sensitive system to assess and quantify infection by flow cytometry. Evaluation of a panel of mutant Chinese hamster ovary cell lines that are genetically deficient in various aspects of GAG synthesis showed that infection was reduced up to 80% depending on the type of GAG deficiency. Enzymatic removal of heparan sulfate and/or chondroitin sulfate from the surface of HEp-2 cells also reduced infection, and the removal of both reduced infection even further. Blocking experiments in which RSV was preincubated with various soluble GAGs revealed the relative blocking order of: heparin > heparan sulfate > chondroitin sulfate B. Iduronic acid is a component common to these GAGs. GAGs that do not contain iduronic acid, namely, chondroitin sulfate A and C and hyaluronic acid, did not inhibit infection. A role for iduronic acid-containing GAGs in RSV infection was confirmed by the ability of basic fibroblast growth factor to block infection, because basic fibroblast growth factor binds to GAGs containing iduronic acid. Pretreatment of cells with protamine sulfate, which binds and blocks GAGs, also reduced infection. In these examples, infection was reduced by pretreatment of the virus with soluble GAGs, pretreatment of the cells with GAG-binding molecules, pretreatment of the cells with GAG-destroying enzymes or in cells genetically deficient in GAGs. These results establish that the GAGs involved in RSV infection are present on the cell rather than on the virus particle. Thus, the presence of cell surface GAGs containing iduronic acid, like heparan sulfate and chondroitin sulfate B, is required for efficient RSV infection in cell culture.
呼吸道合胞病毒(RSV)是一种重要的人类呼吸道病原体,对婴儿尤其如此。糖胺聚糖(GAGs)被认为与培养细胞的RSV感染起始有关,但尚不清楚涉及何种类型的GAGs及其成分,重要的GAGs是存在于病毒还是细胞上,以及它们对感染的贡献程度如何。我们构建并拯救了一种表达重组绿色荧光蛋白(GFP)的RSV(rgRSV),并使用该病毒开发了一种灵敏的系统,通过流式细胞术评估和量化感染情况。对一组在GAG合成的各个方面存在基因缺陷的突变中国仓鼠卵巢细胞系进行评估,结果表明,根据GAG缺陷的类型,感染率可降低达80%。用酶从HEp-2细胞表面去除硫酸乙酰肝素和/或硫酸软骨素也会降低感染,同时去除两者会进一步降低感染。在阻断实验中,将RSV与各种可溶性GAGs预孵育,结果显示相对阻断顺序为:肝素>硫酸乙酰肝素>硫酸软骨素B。艾杜糖醛酸是这些GAGs的共同成分。不含艾杜糖醛酸的GAGs,即硫酸软骨素A和C以及透明质酸,不会抑制感染。碱性成纤维细胞生长因子能够阻断感染,证实了含艾杜糖醛酸的GAGs在RSV感染中的作用,因为碱性成纤维细胞生长因子可与含艾杜糖醛酸的GAGs结合。用硫酸鱼精蛋白预处理细胞,硫酸鱼精蛋白可结合并阻断GAGs,这也会降低感染。在这些例子中,通过用可溶性GAGs预处理病毒、用GAG结合分子预处理细胞以及用GAG破坏酶预处理细胞或在GAGs基因缺陷的细胞中,感染率均有所降低。这些结果表明,参与RSV感染的GAGs存在于细胞而非病毒颗粒上。因此,在细胞培养中,高效的RSV感染需要存在含艾杜糖醛酸的细胞表面GAGs,如硫酸乙酰肝素和硫酸软骨素B。