A mammalian fibroblast zoo reveals barriers to cross-species virus replication and differential regulation of antiviral immunity

Virus zoonosis represents a continual threat to humans. Viruses emerge in humans directly or indirectly through interactions with mammals. However, our understanding of virus-host susceptibility across the diversity of mammals is limited and experimental model systems are restricted to a very small set of model organisms. Mammals are highly diverse and different habitats, lifestyles, diets, and exposures to different pathogens have driven substantial genetic diversity. We generated a library of primary fibroblasts across 86 mammalian species and used these cells to build an atlas of virus-host susceptibility across a panel of arboviruses that infect diverse mammals including humans. Perturbing the innate immune system revealed some virus-host pairs where restriction is controlled by the immune system and others where there is an incompatibility with host factors. Transcriptomic profiling of the library in response to virus sensing mimicked by poly(I:C) or antiviral signaling with type I interferon reveals a core set of conserved genes that respond as well as substantial species- and order-specific responses. Together these data provide a comparative atlas of innate immune responses across mammals and offer a window into how these systems have evolved across animals.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-11-06
DOI
https://doi.org/10.64898/2026.11.04.763981
Primary Topic
interferon and immune responses
Type
preprint

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preprint

A mammalian fibroblast zoo reveals barriers to cross-species virus replication and differential regulation of antiviral immunity

Stephanie H. Zec, Ryan Andrew Langlois, Matthew T. Aliota, Jordan T. Becker et al.
bioRxiv (Cold Spring Harbor Laboratory)
interferon and immune responses
preprint

A mammalian fibroblast zoo reveals barriers to cross-species virus replication and differential regulation of antiviral immunity

Stephanie H. Zec, Ryan Andrew Langlois, Matthew T. Aliota, Jordan T. Becker, Charles M. Rice, Arno Wuenschmann, Michael Gale, Nakarin Pamornchainavakul, Swechha Mainali Pokharel, Clayton K. Mickelson, Frances K. Shepherd, Adam J. Gilbertsen, H.-H. Hoffmann, Jan Komorowski, Sara R. Cherry, Cera A. McDonald, Kenneth H. Dinnon, Anne E. Rivas, Dira S. Putri, Mark J. Pierson, Mark Salnikov, Lauren M. Pross, Yue Li, Tristan T Neal, Girish Pulinkala, Timo Schoon, Esther Vogt, Kayla Hoffman, Susie Garity, Georgia McClain, Jim Rasmussen
preprint en

Abstract

Virus zoonosis represents a continual threat to humans. Viruses emerge in humans directly or indirectly through interactions with mammals. However, our understanding of virus-host susceptibility across the diversity of mammals is limited and experimental model systems are restricted to a very small set of model organisms. Mammals are highly diverse and different habitats, lifestyles, diets, and exposures to different pathogens have driven substantial genetic diversity. We generated a library of primary fibroblasts across 86 mammalian species and used these cells to build an atlas of virus-host susceptibility across a panel of arboviruses that infect diverse mammals including humans. Perturbing the innate immune system revealed some virus-host pairs where restriction is controlled by the immune system and others where there is an incompatibility with host factors. Transcriptomic profiling of the library in response to virus sensing mimicked by poly(I:C) or antiviral signaling with type I interferon reveals a core set of conserved genes that respond as well as substantial species- and order-specific responses. Together these data provide a comparative atlas of innate immune responses across mammals and offer a window into how these systems have evolved across animals.

bioRxiv (Cold Spring Harbor Laboratory)
Uppsala University (SE), University of Minnesota (US), Minnesota Zoo (US), University of Pennsylvania (US), Rockefeller University (US)
National Heart, Lung, and Blood Institute
Good health and well-being
interferon and immune responses
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