KDM6A is required for highly pathogenic coronavirus infection in Huh7.5 cells.

  • Jin Wei (424761)
  • Mia Madel Alfajaro (10319201)
  • Wesley L. Cai (5597987)
  • Vincent R. Graziano (8677380)
  • Madison S. Strine (8677383)
  • Renata B. Filler (8677386)
  • Scott B. Biering (7165010)
  • Sylvia A. Sarnik (16502840)
  • Sonam Patel (14909265)
  • Bridget L. Menasche (16502843)
  • Susan R. Compton (11747702)
  • Silvana Konermann (9683935)
  • Patrick D. Hsu (16324564)
  • Robert C. Orchard (8677401)
  • Qin Yan (281622)
  • Craig B. Wilen (8677404)
Publication date
July 2023
Publisher
Public Library of Science (PLoS)

Abstract

(A) KDM6A expression in KDM6A polyclonal KO Huh7.5 cells. (B) KDM6A polyclonal KO Huh7.5 cells were infected with icSARS-CoV-2-mNeonGreen at an MOI of 1. Infected cells were imaged via fluorescence microscopy (left) and mNeonGreen expressing cell frequency was measured 2 dpi (right). Scale bar: 300 μm. (C) Huh7.5 cells were infected with SARS-CoV-2 at an MOI of 0.1 for 1 dpi. Virus titer was measured by plaque assays. (D) KDM6A polyclonal Huh7.5 E6 cells were infected with SARS-CoV-2 (left), HKU5-SARS-CoV-1-S (middle) and MERS-CoV (right) at an MOI of 0.2. Cell viability relative to a mock infected control was measured 3 dpi with CellTiter Glo. (E) KDM6A polyclonal Huh7.5 E6 cells were infected with VSV peudovirus (VSVpp): VSV-G, SARS-CoV-2...

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