The CCR5 and CXCR4 coreceptors are both used by human immunodeficiency virus type 1 primary isolates from subtype C

被引:143
|
作者
Cilliers, T
Nhlapo, J
Coetzer, M
Orlovic, D
Ketas, T
Olson, WC
Moore, JP
Trkola, A
Morris, L
机构
[1] Natl Inst Communicable Dis, AIDS Virus Res Unit, ZA-2131 Johannesburg, South Africa
[2] Sizwe Infect Dis Hosp, Johannesburg, South Africa
[3] Progen Pharmaceut Inc, Tarrytown, NY USA
[4] Cornell Univ, Weill Med Coll, Dept Microbiol & Immunol, New York, NY USA
[5] Univ Zurich Hosp, Div Infect Dis, CH-8091 Zurich, Switzerland
[6] Univ Zurich Hosp, Hosp Epidemiol, CH-8091 Zurich, Switzerland
基金
英国惠康基金;
关键词
D O I
10.1128/JVI.77.7.4449-4456.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Human immunodeficiency virus type 1 (HIV-1) subtype C viruses with different coreceptor usage profiles were isolated from 29 South African patients with advanced AIDS. All 24 R5 isolates were inhibited by the CCR5-specific agents, PRO 140 and RANTES, while the two X4 viruses and the three R5X4 viruses were sensitive to the CXCR4-specific inhibitor, AMD3100. The five X4 or R5X4 viruses were all able to replicate in peripheral blood mononuclear cells that did not express CCR5. When tested using coreceptor-transfected cell lines, one R5 virus was also able to use CXCR6, and another R5X4 virus could use CCR3, BOB/GPR15, and CXCR6. The R5X4 and X4 viruses contained more-diverse V3 loop sequences, with a higher overall positive charge, than the R5 viruses. Hence, some HIV-1 subtype C viruses are able to use CCR5, CXCR4, or both CXCR4 and CCR5 for entry, and they are sensitive to specific inhibitors of entry via these coreceptors. These observations are relevant to understanding the rapid spread of HIV-1 subtype C in the developing world and to the design of intervention and treatment strategies.
引用
收藏
页码:4449 / 4456
页数:8
相关论文
共 50 条
  • [21] Cooperation of multiple CCR5 coreceptors is required for infections by human immunodeficiency virus type 1
    Kuhmann, SE
    Platt, EJ
    Kozak, SL
    Kabat, D
    JOURNAL OF VIROLOGY, 2000, 74 (15) : 7005 - 7015
  • [22] CXCR4 or CCR5 tropism of human immunodeficiency virus type 1 isolates does not determine the immunological milieu in patients responding to antiretroviral therapy
    Price, Patricia
    Keane, Niamh
    Gray, Lachlan
    Lee, Silvia
    Gorry, Paul R.
    French, Martyn A.
    VIRAL IMMUNOLOGY, 2006, 19 (04) : 734 - 740
  • [23] Exclusion of HIV coreceptors CXCR4, CCR5, and CCR3 from the HIV envelope
    Lallos, LB
    Laal, S
    Hoxie, JA
    Zolla-Pazner, S
    Bandres, JC
    AIDS RESEARCH AND HUMAN RETROVIRUSES, 1999, 15 (10) : 895 - 897
  • [24] Thalidomide suppresses up-regulation of human immunodeficiency virus coreceptors CXCR4 and CCR5 on CD4+ T cells in humans
    Juffermans, NP
    Verbon, A
    Olszyna, DP
    van Deventer, SJH
    Speelman, P
    van der Poll, T
    JOURNAL OF INFECTIOUS DISEASES, 2000, 181 (05): : 1813 - 1816
  • [25] Increased density of human immunodeficiency virus type 1 coreceptors CCR5 and CXCR4 on the surfaces of CD4+ T cells and monocytes of patients with Schistosoma mansoni infection
    Secor, WE
    Shah, A
    Mwinzi, PMN
    Ndenga, BA
    Watta, CO
    Karanja, DMS
    INFECTION AND IMMUNITY, 2003, 71 (11) : 6668 - 6671
  • [26] The HIV coreceptors CXCR4 and CCR5 are differentially expressed and regulated on human T lymphocytes
    Bleul, CC
    Wu, LJ
    Hoxie, JA
    Springer, TA
    Mackay, CR
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (05) : 1925 - 1930
  • [27] HIV-1 coreceptors CCR5 and CXCR4 both mediate neuronal cell death but CCR5 paradoxically can also contribute to protection
    M Kaul
    Q Ma
    K E Medders
    M K Desai
    S A Lipton
    Cell Death & Differentiation, 2007, 14 : 296 - 305
  • [28] HIV-1 coreceptors CCR5 and CXCR4 both mediate neuronal cell death but CCR5 paradoxically can also contribute to protection
    Kaul, M.
    Ma, Q.
    Medders, K. E.
    Desai, M. K.
    Lipton, S. A.
    CELL DEATH AND DIFFERENTIATION, 2007, 14 (02): : 296 - 305
  • [29] Glycosphingolipids promote entry of a broad range of human immunodeficiency virus type 1 isolates into cell lines expressing CD4, CXCR4 and/or CCR5
    Hug, P
    Lin, HMJ
    Korte, T
    Xiao, X
    Dimitrov, D
    Wang, JM
    Puri, A
    Blumenthal, R
    MOLECULAR BIOLOGY OF THE CELL, 1999, 10 : 300A - 300A
  • [30] Glycosphingolipids promote entry of a broad range of human immunodeficiency virus type 1 isolates into cell lines expressing CD4, CXCR4, and/or CCR5
    Hug, P
    Lin, HMJ
    Korte, T
    Xiao, XD
    Dimitrov, DS
    Wang, JM
    Puri, A
    Blumenthal, R
    JOURNAL OF VIROLOGY, 2000, 74 (14) : 6377 - 6385