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SARS-CoV-2 triggers DNA damage response in Vero E6 cells
Joshua Victor; Jamie Deutsch; Annalis Whitaker; Erica N Lamkin; Anthony March; Pei Zhou; Jason W Botten; Nimrat Chatterjee.
Afiliação
  • Joshua Victor; University of Vermont
  • Jamie Deutsch; University of Vermont
  • Annalis Whitaker; University of Vermont
  • Erica N Lamkin; University of Vermont
  • Anthony March; University of Vermont
  • Pei Zhou; Duke University School of Medicine
  • Jason W Botten; University of Vermont
  • Nimrat Chatterjee; University of Vermont
Preprint em En | PREPRINT-BIORXIV | ID: ppbiorxiv-459535
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ABSTRACT
The novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus responsible for the current COVID-19 pandemic and has now infected more than 200 million people with more than 4 million deaths globally. Recent data suggest that symptoms and general malaise may continue long after the infection has ended in recovered patients, suggesting that SARS-CoV-2 infection has profound consequences in the host cells. Here we report that SARS-CoV-2 infection can trigger a DNA damage response (DDR) in African green monkey kidney cells (Vero E6). We observed a transcriptional upregulation of the Ataxia telangiectasia and Rad3 related protein (ATR) in infected cells. In addition, we observed enhanced phosphorylation of CHK1, a downstream effector of the ATR DNA damage response, as well as H2AX. Strikingly, SARS-CoV-2 infection lowered the expression of TRF2 shelterin-protein complex, and reduced telomere lengths in infected Vero E6 cells. Thus, our observations suggest SARS-CoV-2 may have pathological consequences to host cells beyond evoking an immunopathogenic immune response.
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Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-BIORXIV Tipo de estudo: Observational_studies / Prognostic_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Preprint
Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-BIORXIV Tipo de estudo: Observational_studies / Prognostic_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Preprint