# Arf GTPases Define BST-2-Independent Pathways for HIV-1 Assembly and Release

## TL;DR

This study shows that Arf1 and Arf6 proteins are essential for HIV-1 assembly and release, independent of the host protein BST-2.

## Contribution

The paper identifies Arf1- and Arf6-mediated trafficking pathways as critical for HIV-1 assembly and release, independent of BST-2.

## Key findings

- Arf1 and Arf6 are required for efficient trafficking of HIV-1 Gag polyprotein and virion production.
- Disruption of Arf1 or Arf6 activity does not affect BST-2 expression or distribution.
- Dynamic transitions between GTP- and GDP-bound states of Arf1 are essential for productive Gag trafficking.

## Abstract

ADP-ribosylation factor (Arf) proteins are small GTPases that regulate intracellular membrane trafficking and actin remodeling through tightly controlled cycles of GTP binding and hydrolysis. Arf1, a central coordinator of Golgi and endosomal transport, and Arf6, which regulates plasma membranes and endosomal dynamics, have both been implicated in late stages of the HIV-1 life cycle. However, the mechanisms by which these GTPases support viral assembly and release remain incompletely defined. Here, we provide direct evidence that both Arf1 and Arf6 are required for efficient trafficking of the HIV-1 Gag polyprotein, assembly, and virion production. Perturbation of Arf1 function using either GTP-locked (Q71L) or GDP-locked (T31N) mutants significantly reduced virus release, impaired Gag association with membrane compartments, and prevented its accumulation at the plasma membrane. Manipulation of Arf1 cycling through the GTPase-activating protein AGAP1 further demonstrated that dynamic transitions between GTP- and GDP-bound states are essential for productive Gag trafficking. Similarly, expression of a constitutively active Arf6 mutant (Q67L) misrouted Gag to intracellular membranes and markedly suppressed virion release. Importantly, disruption of Arf1 or Arf6 activity did not affect the expression, surface levels, or intracellular distribution of the host restriction factor BST-2. Together, these findings identify Arf1- and Arf6-mediated trafficking pathways as critical host determinants of HIV-1 assembly and release and establish that their functions operate independently of BST-2 antagonism.