Owl monkey CCR5 reveals synergism between CD4 and CCR5 in HIV-1 entry

Virology. 2017 Dec:512:180-186. doi: 10.1016/j.virol.2017.09.018.

Abstract

Studying HIV-1 replication in the presence of functionally related proteins from different species has helped define host determinants of HIV-1 infection. Humans and owl monkeys, but not macaques, encode a CD4 receptor that permits entry of transmissible HIV-1 variants due to a single residue difference. However, little is known about whether divergent CCR5 receptor proteins act as determinants of host-range. Here we show that both owl monkey (Aotus vociferans) CD4 and CCR5 receptors are functional for the entry of transmitted HIV-1 when paired with human versions of the other receptor. By contrast, the owl monkey CD4/CCR5 pair is generally a suboptimal receptor combination, although there is virus-specific variation in infection with owl monkey receptors. Introduction of the human residues 15Y and 16T within a sulfation motif into owl monkey CCR5 resulted in a gain of function. These findings suggest there is cross-talk between CD4 and CCR5 involving the sulfation motif.

Keywords: CCR5; CD4; Entry; HIV-1; Owl monkey; Receptor; Species differences.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Aotidae
  • CD4 Antigens / physiology*
  • HEK293 Cells
  • HIV-1 / physiology*
  • Humans
  • Mutation
  • Receptors, CCR5 / genetics
  • Receptors, CCR5 / metabolism*
  • Virus Internalization*
  • Virus Replication

Substances

  • CD4 Antigens
  • Receptors, CCR5