Position 22 of the V3 loop is associated with HIV infectivity

被引:1
|
作者
Wei, Xue-Mei [1 ]
Xu, Hua-Feng [2 ]
Cheng, Xue-Di [1 ]
Bu, Nan [3 ]
Zhou, Hai-Zhou [1 ]
机构
[1] Harbin Med Univ, Affiliated Hosp 1, Dept Lab Diag, 23 Youzheng St, Harbin 150001, Heilongjiang, Peoples R China
[2] Heilongjiang Prov Hosp, Dept Lab Diag, Harbin 150081, Heilongjiang, Peoples R China
[3] Jiamusi Cent Hosp, Dept Digest Med, Jiamusi 154002, Heilongjiang, Peoples R China
基金
中国国家自然科学基金;
关键词
DISEASE PROGRESSION; ENTRY INHIBITORS; CORECEPTOR USAGE; CCR5; CORECEPTOR; GP120; CROWN; TROPISM; RECOGNITION; RECEPTORS; PHENOTYPE;
D O I
10.1007/s00705-016-3138-7
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Human immunodeficiency virus subtype 1B (HIV-1B) binds to the CD4 receptor and co-receptor CCR5 or CXCR4 to enter T lymphocytes. The amino acid sequence of the HIV envelope glycoprotein V3 region determines the co-receptor tropism, thereby influencing the infectivity of the virus. Our research group previously found that the amino acid at position 22 of the V3 region may affect the infectivity of the virus, and in this study, we tested this hypothesis. We constructed pseudoviruses by changing the amino acids at position 22 of the V3 region in CCR5-tropic and CXCR4-tropic viruses and tested their infectivity. When the amino acid at V3 position 22 was altered in the CCR5- and CXCR4-tropic viruses, their ability to infect cells decreased to 20.6% and 17.14%, respectively. Therefore, we propose that residue 22 in the V3 region of subtype HIV-1B significantly influences the infectivity of the virus.
引用
收藏
页码:637 / 643
页数:7
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