CD164 is an endolysomal host factor for entry of Clade A New World Arenaviruses

Arenaviruses are divided into Old World (OW) and New World (NW) groups. OW arenaviruses enter cells through a pH-dependent receptor switch from a plasma-membrane factor to an endolysosomal receptor for subsequent membrane fusion, whereas clade B NW arenaviruses use transferrin receptor 1 without a secondary receptor. Using a vesicular stomatitis virus (VSV) chimera expressing the glycoprotein complex (GPC) of the clade A NW arenavirus Pichindé virus, we performed a genome-wide CRISPR loss-of-function screen and identified the endolysosomal sialomucin CD164 as an essential host factor. CD164 knockout cells were resistant to VSV chimeras bearing the GPCs of Pichindé, Paraná, and Flexal viruses, and to authentic Pichindé and Paraná virus, with susceptibility restored by complementation. The requirement mapped to the cysteine-rich domain of CD164, which bound GP1 in a pH-dependent manner through main-chain interactions. These findings define CD164 as an endolysosomal receptor for clade A NW arenaviruses expanding the receptor switching paradigm.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-04-22
DOI
https://doi.org/10.64898/2026.04.21.719929
Primary Topic
Viral Infections and Outbreaks Research
Type
article
Field-Weighted Citation Impact
0.00

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article

CD164 is an endolysomal host factor for entry of Clade A New World Arenaviruses

Cassandra E. Thompson, Paul W. Rothlauf, Rita M. Meganck, Zhuoming Liu et al.
bioRxiv (Cold Spring Harbor Laboratory)
Viral Infections and Outbreaks Research
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CD164 is an endolysomal host factor for entry of Clade A New World Arenaviruses

Cassandra E. Thompson, Paul W. Rothlauf, Rita M. Meganck, Zhuoming Liu, John G. Doench, Daved H. Fremont, Michael Diamond, Marjorie Cornejo Pontelli, Sean P. J. Whelan, Hongming Ma, Mason A Roth, Tomasz Kaszuba
article en

Abstract

Arenaviruses are divided into Old World (OW) and New World (NW) groups. OW arenaviruses enter cells through a pH-dependent receptor switch from a plasma-membrane factor to an endolysosomal receptor for subsequent membrane fusion, whereas clade B NW arenaviruses use transferrin receptor 1 without a secondary receptor. Using a vesicular stomatitis virus (VSV) chimera expressing the glycoprotein complex (GPC) of the clade A NW arenavirus Pichindé virus, we performed a genome-wide CRISPR loss-of-function screen and identified the endolysosomal sialomucin CD164 as an essential host factor. CD164 knockout cells were resistant to VSV chimeras bearing the GPCs of Pichindé, Paraná, and Flexal viruses, and to authentic Pichindé and Paraná virus, with susceptibility restored by complementation. The requirement mapped to the cysteine-rich domain of CD164, which bound GP1 in a pH-dependent manner through main-chain interactions. These findings define CD164 as an endolysosomal receptor for clade A NW arenaviruses expanding the receptor switching paradigm.

bioRxiv (Cold Spring Harbor Laboratory)
Broad Institute (US), Washington University in St. Louis (US)
National Institute of Allergy and Infectious Diseases
Life in Land
Openalex Percentile: Top 12%
Viral Infections and Outbreaks Research
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