Broad host range of human T-cell leukemia virus type 1 demonstrated with an improved pseudotyping system

被引:77
作者
Sutton, RE
Littman, DR
机构
[1] STANFORD UNIV,DEPT BIOCHEM,STANFORD,CA 94305
[2] UNIV CALIF SAN FRANCISCO,DEPT MICROBIOL & IMMUNOL,SAN FRANCISCO,CA 94143
[3] UNIV CALIF SAN FRANCISCO,DEPT BIOCHEM & BIOPHYS,SAN FRANCISCO,CA 94143
[4] NYU,MED CTR,HOWARD HUGHES MED INST,NEW YORK,NY 10016
[5] NYU,MED CTR,SKIRBALL INST BIOMOL MED,NEW YORK,NY 10016
关键词
D O I
10.1128/JVI.70.10.7322-7326.1996
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Studies of human T-cell leukemia virus type 1 (HTLV-1) have been hampered by the difficultly of achieving high cell-free and cell-associated infectious titers. Current retroviral pseudotyping systems using the HTLV-1 envelope generate titers of less than 200 infectious particles per ml. We describe here an improved system for pseudotyping using a defective human immunodeficiency virus (HIV) type 1 genome in combination with HTLV-1 env in 293T producer cells, Introduction of additional copies of rer and treatment of cells with sodium butyrate resulted in a cell-associated titer of 10(5)/ml and cell-free titers of greater than 10(4)/ml. By using this system, we found that the host range of HTLV-1 is even greater than previously suspected, Earlier studies which assigned a chromosomal location for the HTLV-1 receptor may therefore reflect cell-to-cell variation in receptor number rather than the absolute presence or absence of a receptor. The generation of higher-titer HIV(HTLV-1) may facilitate identification of the cellular receptor and investigations of the pathophysiology of HTLV-1 infection.
引用
收藏
页码:7322 / 7326
页数:5
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