AP3B1 Has Type I Interferon-Independent Antiviral Function against SARS-CoV-2

Viruses. 2024 Aug 29;16(9):1377. doi: 10.3390/v16091377.

Abstract

The unprecedented research effort associated with the emergence of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) included several extensive proteomic studies that identified host proteins that interact with individual viral gene products. However, in most cases, the consequences of those virus-host interactions for virus replication were not experimentally pursued, which is a necessary step in determining whether the interactions represent pro- or anti-viral events. One putative interaction commonly identified in multiple studies was between the host adaptor protein complex 3 (AP-3) subunit B1 (AP3B1) and the SARS-CoV-2 envelope protein (E). AP3B1 is one subunit of AP-3 required for the biogenesis of lysosomal-related organelles (LROs), and its function impacts important disease processes including inflammation and vascular health. Thus, interactions between AP3B1 and SARS-CoV-2 might influence the clinical outcomes of infection. To determine if AP3B1 has a role in the SARS-CoV-2 replication cycle, we first confirmed the interaction in virus-infected cells using immunoprecipitation (IP) and immunofluorescence assays (IFA). AP3B1 is required by multiple viruses to aid in the replication cycle and therefore may be a therapeutic target. However, we found that the overexpression of AP3B1 suppressed SARS-CoV-2 replication, whereas the siRNA-mediated depletion of AP3B1 increased the release of infectious virus, suggesting an antiviral role for AP3B1. Together, our findings suggest that AP3B1 is an intrinsic barrier to SARS-CoV-2 replication through interactions with the viral E protein. Our work justifies further investigations of LRO trafficking in SARS-CoV-2 target cells and their role in viral pathogenesis.

Keywords: AP3B1; COVID-19; SARS-CoV-2; antiviral proteins.

MeSH terms

  • Adaptor Protein Complex 3* / genetics
  • Adaptor Protein Complex 3* / metabolism
  • Adaptor Protein Complex beta Subunits / genetics
  • Adaptor Protein Complex beta Subunits / metabolism
  • Animals
  • COVID-19* / immunology
  • COVID-19* / metabolism
  • COVID-19* / virology
  • Chlorocebus aethiops
  • HEK293 Cells
  • Host-Pathogen Interactions
  • Humans
  • Interferon Type I* / metabolism
  • SARS-CoV-2* / physiology
  • Vero Cells
  • Virus Replication*

Substances

  • Adaptor Protein Complex 3
  • Interferon Type I
  • Adaptor Protein Complex beta Subunits