Journal
VIROLOGY
Volume 413, Issue 2, Pages 293-299Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.virol.2011.02.019
Keywords
HIV-1; CCR5; gp120; V3 loop; Viral entry; Maraviroc; Noncompetitive resistance
Categories
Funding
- Ministry of Education, Science, Sports, and Culture
- Ministry of Health Labor, and Welfare, Japan
- Grants-in-Aid for Scientific Research [23590548] Funding Source: KAKEN
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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. (C) 2011 Elsevier Inc. All rights reserved.
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