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Molecular consequences of SARS-CoV-2 liver tropism.

Nicola WannerGeoffroy AndrieuxPau Badia-I-MompelCarolin EdlerSusanne PfefferleMaja T LindenmeyerChristian Schmidt-LauberJan CzogallaMilagros N WongYusuke OkabayashiFabian BraunMarc LütgehetmannElisabeth MeisterShun LuMaria L M NoriegaThomas GüntherAdam GrundhoffNicole FischerHanna BräuningerDiana LindnerDirk WestermannFabian HaasKevin RoedlStefan KlugeMarylyn Martina AddoSamuel HuberAnsgar W LohseJochen ReiserBenjamin OndruschkaJan P SperhakeJulio Saez-RodriguezMelanie BoerriesSalim Salim HayekMartin AepfelbacherPietro ScaturroVictor G PuellesTobias B Huber
Published in: Nature metabolism (2022)
Extrapulmonary manifestations of COVID-19 have gained attention due to their links to clinical outcomes and their potential long-term sequelae 1 . Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) displays tropism towards several organs, including the heart and kidney. Whether it also directly affects the liver has been debated 2,3 . Here we provide clinical, histopathological, molecular and bioinformatic evidence for the hepatic tropism of SARS-CoV-2. We find that liver injury, indicated by a high frequency of abnormal liver function tests, is a common clinical feature of COVID-19 in two independent cohorts of patients with COVID-19 requiring hospitalization. Using autopsy samples obtained from a third patient cohort, we provide multiple levels of evidence for SARS-CoV-2 liver tropism, including viral RNA detection in 69% of autopsy liver specimens, and successful isolation of infectious SARS-CoV-2 from liver tissue postmortem. Furthermore, we identify transcription-, proteomic- and transcription factor-based activity profiles in hepatic autopsy samples, revealing similarities to the signatures associated with multiple other viral infections of the human liver. Together, we provide a comprehensive multimodal analysis of SARS-CoV-2 liver tropism, which increases our understanding of the molecular consequences of severe COVID-19 and could be useful for the identification of organ-specific pharmacological targets.
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