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Transmitted/founder and chronic subtype C HIV-1 use CD4 and CCR5 receptors with equal efficiency and are not inhibited by blocking the integrin α4β7.

Nicholas F Parrish | Craig B Wilen | Lauren B Banks | Shilpa S Iyer | Jennifer M Pfaff | Jesus F Salazar-Gonzalez | Maria G Salazar | Julie M Decker | Erica H Parrish | Anna Berg | Jennifer Hopper | Bhavna Hora | Amit Kumar | Tatenda Mahlokozera | Sally Yuan | Charl Coleman | Marion Vermeulen | Haitao Ding | Christina Ochsenbauer | John C Tilton | Sallie R Permar | John C Kappes | Michael R Betts | Michael P Busch | Feng Gao | David Montefiori | Barton F Haynes | George M Shaw | Beatrice H Hahn | Robert W Doms
PLoS pathogens | 2012

Sexual transmission of human immunodeficiency virus type 1 (HIV-1) most often results from productive infection by a single transmitted/founder (T/F) virus, indicating a stringent mucosal bottleneck. Understanding the viral traits that overcome this bottleneck could have important implications for HIV-1 vaccine design and other prevention strategies. Most T/F viruses use CCR5 to infect target cells and some encode envelope glycoproteins (Envs) that contain fewer potential N-linked glycosylation sites and shorter V1/V2 variable loops than Envs from chronic viruses. Moreover, it has been reported that the gp120 subunits of certain transmitted Envs bind to the gut-homing integrin α4β7, possibly enhancing virus entry and cell-to-cell spread. Here we sought to determine whether subtype C T/F viruses, which are responsible for the majority of new HIV-1 infections worldwide, share biological properties that increase their transmission fitness, including preferential α4β7 engagement. Using single genome amplification, we generated panels of both T/F (n = 20) and chronic (n = 20) Env constructs as well as full-length T/F (n = 6) and chronic (n = 4) infectious molecular clones (IMCs). We found that T/F and chronic control Envs were indistinguishable in the efficiency with which they used CD4 and CCR5. Both groups of Envs also exhibited the same CD4+ T cell subset tropism and showed similar sensitivity to neutralization by CD4 binding site (CD4bs) antibodies. Finally, saturating concentrations of anti-α4β7 antibodies failed to inhibit infection and replication of T/F as well as chronic control viruses, although the growth of the tissue culture-adapted strain SF162 was modestly impaired. These results indicate that the population bottleneck associated with mucosal HIV-1 acquisition is not due to the selection of T/F viruses that use α4β7, CD4 or CCR5 more efficiently.

Pubmed ID: 22693444

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Associated grants

  • Agency: NIAID NIH HHS, United States
    Id: U01 AI067854
  • Agency: NIAID NIH HHS, United States
    Id: T32 AI007632
  • Agency: NIAID NIH HHS, United States
    Id: R01 AI045378
  • Agency: NIAID NIH HHS, United States
    Id: R01 AI040880
  • Agency: NIAID NIH HHS, United States
    Id: P01 AI088564
  • Agency: PHS HHS, United States
    Id: P30 045008
  • Agency: NIAID NIH HHS, United States
    Id: R37 AI045378
  • Agency: NIAID NIH HHS, United States
    Id: P30 AI027763
  • Agency: NIAID NIH HHS, United States
    Id: R01 AI45378
  • Agency: NIAID NIH HHS, United States
    Id: R01 AI40880
  • Agency: NIAID NIH HHS, United States
    Id: P30 AI027767
  • Agency: NIAID NIH HHS, United States
    Id: R01 AI094604

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RRID:SCR_014629

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