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HSV-1 Reconfigures Human Genome to Fuel Its Replication

Blocking topoisomerase I halted HSV-1’s genome reshaping in cell cultures, pointing to a new treatment strategy.

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Overview

  • The virus hijacks RNA polymerase II within the first hour of infection to drive viral protein synthesis.
  • Host chromatin collapses under stolen transcription machinery, compacting the genome to 30% of its original volume by eight hours.
  • Inhibiting the DNA-cutting enzyme topoisomerase I completely stopped HSV-1 from reorganizing host DNA, preventing new viral particle formation in vitro.
  • Nearly four billion people carry HSV-1, with rising drug resistance leaving existing therapies limited to symptom management without a cure.
  • Researchers propose that targeting topoisomerase I could also disrupt similar genome-manipulation tactics used by other DNA viruses.