iScience (Mar 2024)

Simple virus-free mouse models of COVID-19 pathologies and oral therapeutic intervention

  • Huabin Zhu,
  • Anuj K. Sharma,
  • Karina Aguilar,
  • Faizan Boghani,
  • Semih Sarcan,
  • Michelle George,
  • Janavi Ramesh,
  • Joshua Van Der Eerden,
  • Chandramukhi S. Panda,
  • Aileen Lopez,
  • Wenbo Zhi,
  • Roni Bollag,
  • Nikhil Patel,
  • Kandace Klein,
  • Joe White,
  • Muthusamy Thangaraju,
  • Bal L. Lokeshwar,
  • Nagendra Singh,
  • Vinata B. Lokeshwar

Journal volume & issue
Vol. 27, no. 3
p. 109191

Abstract

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Summary: The paucity of preclinical models that recapitulate COVID-19 pathology without requiring SARS-COV-2 adaptation and humanized/transgenic mice limits research into new therapeutics against the frequently emerging variants-of-concern. We developed virus-free models by C57BL/6 mice receiving oropharyngeal instillations of a SARS-COV-2 ribo-oligonucleotide common in all variants or specific to Delta/Omicron variants, concurrently with low-dose bleomycin. Mice developed COVID-19-like lung pathologies including ground-glass opacities, interstitial fibrosis, congested alveoli, and became moribund. Lung tissues from these mice and bronchoalveolar lavage and lung tissues from patients with COVID-19 showed elevated levels of hyaluronic acid (HA), HA-family members, an inflammatory signature, and immune cell infiltration. 4-methylumbelliferone (4-MU), an oral drug for biliary-spasm treatment, inhibits HA-synthesis. At the human equivalent dose, 4-MU prevented/inhibited COVID-19-like pathologies and long-term morbidity; 4-MU and metabolites accumulated in mice lungs. Therefore, these versatile SARS-COV-2 ribo-oligonucleotide oropharyngeal models recapitulate COVID-19 pathology, with HA as its critical mediator and 4-MU as a potential therapeutic for COVID-19.

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