A combination of polymorphic mutations in V3 loop of HIV-1 gp120 can confer noncompetitive resistance to maraviroc

作者：Yuan Yuzhe; Maeda Yosuke; Terasawa Hiromi; Monde Kazuaki; Harada Shinji; Yusa Keisuke^*

来源：Virology, 2011, 413(2): 293-299.

DOI：10.1016/j.virol.2011.02.019

• HIV-1
• CCR5
• gp120
• V3 loop
• Viral entry
• Maraviroc
• Noncompetitive resistance

Maraviroc binds to the pocket of extracellular loops of the cell surface CCR5 and prevents R5 HIV-1 from using CCR5 as a coreceptor for entry into CD4-positive cells. To evaluate the contribution of the V3 loop structure in gp120 to maraviroc resistance, we isolated maraviroc-resistant variants from the V3 loop library virus (HIV-1(V3Lib)) containing a set of random combinations of 0-10 polymorphic mutations in vitro. HIV-1(V31Lib) at passage 17 could not be suppressed even at 10 mu M (> 1400-fold resistance), while HIV-1(JR-FL) at passage 17 revealed an 8-fold resistance to maraviroc. HIV-1(V3Lib-p17) contained T199K and T275M plus 5 mutations in the V3 loop, 1304V/F312W/T314A/E317D/1318V. The profile of pseudotyped virus containing 1304V/F312W/T314A/E317D/1318V in V3 loop alone revealed a typical noncompetitive resistance, although T199K and/or T275M could not confer noncompetitive resistance. This type of library virus is useful for isolation of escape viruses from effective entry inhibitors.

• 出版日期2011-5-10