Host cell glycosylation selects for infection with CCR5- versus CXCR4-tropic HIV-1.

ABSTRACT: Human immunodeficiency virus type 1 (HIV-1) infection involves a selection bottleneck that leads to transmission of one or a few variants. C-C motif chemokine receptor 5 (CCR5) or C-X-C motif chemokine receptor 4 (CXCR4) can act as coreceptors for HIV-1 viral entry. However, initial infection mostly occurs via CCR5, despite abundant expression of CXCR4 on target cells. The host factors that influence HIV-1 susceptibility and selection during transmission are unclear. Here we conduct CRISPR-Cas9 screens and identify SLC35A2 (a transporter of UDP-galactose expressed in target cells in blood and mucosa) as a potent and specific CXCR4-tropic restriction factor in primary target CD4⁺ T cells. SLC35A2 inactivation, which resulted in truncated glycans, not only increased CXCR4-tropic i

SUBMITTER: Itell HL 

PROVIDER: S-EPMC12335854 | biostudies-literature | 2024 Nov

REPOSITORIES: biostudies-literature