Adaptation of HIV-1 to cells with low expression of the CCR5 coreceptor

被引:8
作者
Espy, Nicole [1 ]
Pacheco, Beatriz [2 ,3 ]
Sodroski, Joseph [1 ,2 ,3 ]
机构
[1] Harvard TH Chan Sch Publ Hlth, Dept Immunol & Infect Dis, Boston, MA USA
[2] Dana Farber Canc Inst, Dept Canc Immunol & Virol, Boston, MA 02115 USA
[3] Harvard Med Sch, Dept Microbiol & Immunobiol, Boston, MA USA
基金
美国国家卫生研究院;
关键词
CD4; Trigger; Receptor; Virus entry; Membrane fusion; IMMUNODEFICIENCY-VIRUS TYPE-1; ENVELOPE GLYCOPROTEIN INCORPORATION; SHORT-TERM MONOTHERAPY; CRYO-EM STRUCTURE; DRUG-BOUND CCR5; NEUTRALIZATION SENSITIVITY; CD4; INDEPENDENCE; MARAVIROC-RESISTANT; EXTRACELLULAR LOOP; FUSION INHIBITORS;
D O I
10.1016/j.virol.2017.04.033
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
binding of the human immunodeficiency virus (HIV-1) envelope glycoprotein (Env) trimer ((gp120/gp41)(3)) to the receptors CD4 and CCR5 triggers virus entry into host cells. To identify Env regions that respond to CCR5 binding, HIV-1 was serially passaged on a CD4-positive canine cell line expressing progressively lower levels of CCR5. HIV-1 replication was observed in cells expressing similar to 1300 CCR5 molecules/cell. Env changes that conferred this low-CCR5 replication phenotype were located outside of the known CCR5-binding region of the gp120 Env subunit and did not apparently increase CCR5 binding affinity. The adaptation-associated changes, located in the gp120 alpha 1 helix and in the gp41 HR1 heptad repeat and membrane-proximal external region (MPER), enhanced HIV-1 replication in cells at all levels of CCR5 expression. The adapted Envs exhibited a greater propensity to undergo conformational changes, as evidenced by increased exposure of conserved regions near the CD4- and CCR5-binding sites.
引用
收藏
页码:90 / 107
页数:18
相关论文
共 110 条
[21]   Determination of essential amino acids involved in the CD4-independent tropism of the X4 human immunodeficiency virus type 1 m7NDK isolate: Role of potential N glycosylations in the C2 and V3 regions of gp120 [J].
Dumonceaux, J ;
Goujon, C ;
Joliot, V ;
Briand, P ;
Hazan, U .
JOURNAL OF VIROLOGY, 2001, 75 (11) :5425-5428
[22]   Truncation of the cytoplasmic domain induces exposure of conserved regions in the ectodomain of human immunodeficiency virus type 1 envelope protein [J].
Edwards, TG ;
Wyss, S ;
Reeves, JD ;
Zolla-Pazner, S ;
Hoxie, JA ;
Doms, RW ;
Baribaud, F .
JOURNAL OF VIROLOGY, 2002, 76 (06) :2683-2691
[23]   Relationships between CD4 independence, neutralization sensitivity, and exposure of a CD4-induced epitope in a human immunodeficiency virus type 1 envelope protein [J].
Edwards, TG ;
Hoffman, TL ;
Baribaud, F ;
Wyss, S ;
LaBranche, CC ;
Romano, J ;
Adkinson, J ;
Sharron, M ;
Hoxie, JA ;
Doms, RW .
JOURNAL OF VIROLOGY, 2001, 75 (11) :5230-5239
[24]   Human Immunodeficiency Virus Type 1 V1-to-V5 Envelope Variants from the Chronic Phase of Infection Use CCR5 and Fuse More Efficiently than Those from Early after Infection [J].
Etemad, Behzad ;
Fellows, Angela ;
Kwambana, Brenda ;
Kamat, Anupa ;
Feng, Yang ;
Lee, Sandra ;
Sagar, Manish .
JOURNAL OF VIROLOGY, 2009, 83 (19) :9694-9708
[25]   Efficacy of short-term monotherapy with maraviroc, a new CCR5 antagonist, in patients infected with HIV-1 [J].
Fätkenheuer, G ;
Pozniak, AL ;
Johnson, MA ;
Plettenberg, A ;
Staszewski, S ;
Hoepelman, AIM ;
Saag, MS ;
Goebel, FD ;
Rockstroh, JK ;
Dezube, BJ ;
Jenkins, TM ;
Medhurst, C ;
Sullivan, JF ;
Ridgway, C ;
Abel, S ;
James, IT ;
Youle, M ;
van der Ryst, E .
NATURE MEDICINE, 2005, 11 (11) :1170-1172
[26]   HIV-1 Entry Cofactor: Functional cDNA Cloing of a Seven-Transmembrane, G protein-Coupled Receptor [J].
Feng, Yu ;
Broder, Christopher C. ;
Kennedy, Paul E. ;
Berger, Edward A. .
JOURNAL OF IMMUNOLOGY, 2011, 186 (11) :872-877
[27]   CHARACTERIZATION OF THE FUSION DOMAIN OF THE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 ENVELOPE GLYCOPROTEIN GP41 [J].
FREED, EO ;
MYERS, DJ ;
RISSER, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (12) :4650-4654
[28]   Capture of an early fusion-active conformation of HIV-1 gp41 [J].
Furuta, RA ;
Wild, CT ;
Weng, YK ;
Weiss, CD .
NATURE STRUCTURAL BIOLOGY, 1998, 5 (04) :276-279
[29]   Universal Amplification, Next-Generation Sequencing, and Assembly of HIV-1 Genomes [J].
Gall, Astrid ;
Ferns, Bridget ;
Morris, Clare ;
Watson, Simon ;
Cotten, Matthew ;
Robinson, Mark ;
Berry, Neil ;
Pillay, Deenan ;
Kellam, Paul .
JOURNAL OF CLINICAL MICROBIOLOGY, 2012, 50 (12) :3838-3844
[30]   New Insights into the Mechanisms whereby Low Molecular Weight CCR5 Ligands Inhibit HIV-1 Infection [J].
Garcia-Perez, Javier ;
Rueda, Patricia ;
Staropoli, Isabelle ;
Kellenberger, Esther ;
Alcami, Jose ;
Arenzana-Seisdedos, Fernando ;
Lagane, Bernard .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (07) :4978-4990