Phosphatidylserine receptors are critical for lethal infection by Crimean-Congo hemorrhagic fever virus

The tick-borne Crimean-Congo hemorrhagic fever virus (CCHFV) causes severe and often fatal hemorrhagic disease for which no approved countermeasures are available. Herein, we identify the phosphatidylserine receptors (PSRs) AXL, TIM-1, and TIM-4 as critical entry host factors for CCHFV in cell lines and liver-derived primary cell cultures. Small-molecule and antibody-based PSR inhibitors greatly reduced viral infection in cell culture. Germline knockout of individual PSR genes afforded partial protection against CCHFV infection, disease, and death in a murine model of lethal viral challenge. Mice engineered to lack two PSRs were completely protected from challenge, with viremia and viral replication, pathology, and inflammation in the liver and spleen reduced to baseline. Therefore, PSRs are collectively indispensable for CCHFV infection and pathogenesis. We conclude that PSRs are not just cell entry factors but bona fide determinants of infection, dissemination, and disease by CCHFV and legitimate targets for the development of new antiviral countermeasures.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-10-30
DOI
https://doi.org/10.64898/2026.10.29.762781
Primary Topic
Viral Infections and Vectors
Type
preprint

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preprint

Phosphatidylserine receptors are critical for lethal infection by Crimean-Congo hemorrhagic fever virus

Jacob L. Berrigan, Wendy J. Maury, Stephanie R. Monticelli, Susan Rajnik Coyne et al.
1 links
bioRxiv (Cold Spring Harbor Laboratory)
Viral Infections and Vectors
preprint

Phosphatidylserine receptors are critical for lethal infection by Crimean-Congo hemorrhagic fever virus

Jacob L. Berrigan, Wendy J. Maury, Stephanie R. Monticelli, Susan Rajnik Coyne, Andrew S. Herbert, Ezgi Kaşıkcı, Russell R. Bakken, Christopher P. Stefan, Kartik Chandran, Sarah B. Sulkosky, Kevin Xiankun Zeng, Ana I. Kuehne, Taylor S. Powell, Paige T. Donovan, Matt Daileg Ramirez
preprint en

Abstract

The tick-borne Crimean-Congo hemorrhagic fever virus (CCHFV) causes severe and often fatal hemorrhagic disease for which no approved countermeasures are available. Herein, we identify the phosphatidylserine receptors (PSRs) AXL, TIM-1, and TIM-4 as critical entry host factors for CCHFV in cell lines and liver-derived primary cell cultures. Small-molecule and antibody-based PSR inhibitors greatly reduced viral infection in cell culture. Germline knockout of individual PSR genes afforded partial protection against CCHFV infection, disease, and death in a murine model of lethal viral challenge. Mice engineered to lack two PSRs were completely protected from challenge, with viremia and viral replication, pathology, and inflammation in the liver and spleen reduced to baseline. Therefore, PSRs are collectively indispensable for CCHFV infection and pathogenesis. We conclude that PSRs are not just cell entry factors but bona fide determinants of infection, dissemination, and disease by CCHFV and legitimate targets for the development of new antiviral countermeasures.

bioRxiv (Cold Spring Harbor Laboratory)
University of Iowa (US), Henry M. Jackson Foundation (US), Albert Einstein College of Medicine (US), United States Army Medical Research Institute of Infectious Diseases (US), Montefiore Einstein Comprehensive Cancer Center (US)
National Institute of Allergy and Infectious Diseases
Good health and well-being
Viral Infections and Vectors
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