Spatial and single-cell transcriptomics illuminate bat immunity and barrier tissue evolution
Roy LevingeriD, Dafna Tussia-CoheniD, Sivan FriedmaniD, Yan LenderiD, Yomiran NissaniD, Evgeny FraimovitchiD, Yuval GavrieliD, Jacqueline L.E. TearleiD, Aleksandra A. KolodziejczykiD, Kyung‐Mee MooniD, Tomás GomesiD, Natalia Kunowska, Maya WeinbergiD, Giacomo DonatiiD, Leonard J. FosteriD, Kylie Renee JamesiD, Yossi YoveliD, Tzachi HagaiiD
Abstract
The Egyptian fruit bat displays tolerance to lethal viruses and unique dietary adaptations, but the molecular basis for this is poorly understood. To this end, we generated detailed maps of bat gut, lung and blood cells using spatial and single-cell transcriptomics. We compared bat with mouse and human cells to reveal divergence in genetic programs associated with environmental interactions and immune responses. Complement system genes are transcriptionally divergent, uniquely expressed in bat lung and gut epithelium, and undergo rapid coding-sequence evolution. Specifically in the tip of the gut villus, bat enterocytes express evolutionarily young genes while lacking expression of genes related to specific nutrient absorption. Profiling immune stimulation of PBMCs revealed a monocyte subset with conserved cross-species interferon expression, suggesting strong constraints to avoid an excessive immune response. Our study thus uncovers conserved and divergent immune pathways in bat tissues, providing a unique resource to study bat immunity and evolution.
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