Antiviral Effect of Antimicrobial Peptoid TM9 and Murine Model of Respiratory Coronavirus Infection.
Maxim LebedevAaron B BenjaminSathish KumarNatalia MolchanovaJennifer S LinKent J KosterJulian L LeibowitzAnnelise E BarronJeffrey D CirilloPublished in: Pharmaceutics (2024)
New antiviral agents are essential to improving treatment and control of SARS-CoV-2 infections that can lead to the disease COVID-19. Antimicrobial peptoids are sequence-specific oligo- N -substituted glycine peptidomimetics that emulate the structure and function of natural antimicrobial peptides but are resistant to proteases. We demonstrate antiviral activity of a new peptoid (TM9) against the coronavirus, murine hepatitis virus (MHV), as a closely related model for the structure and antiviral susceptibility profile of SARS-CoV-2. This peptoid mimics the human cathelicidin LL-37, which has also been shown to have antimicrobial and antiviral activity. In this study, TM9 was effective against three murine coronavirus strains, demonstrating that the therapeutic window is large enough to allow the use of TM9 for treatment. All three isolates of MHV generated infection in mice after 15 min of exposure by aerosol using the Madison aerosol chamber, and all three viral strains could be isolated from the lungs throughout the 5-day observation period post-infection, with the peak titers on day 2. MHV-A59 and MHV-A59-GFP were also isolated from the liver, heart, spleen, olfactory bulbs, and brain. These data demonstrate that MHV serves as a valuable natural murine model of coronavirus pathogenesis in multiple organs, including the brain.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- staphylococcus aureus
- escherichia coli
- endothelial cells
- white matter
- heart failure
- resting state
- type diabetes
- coronavirus disease
- electronic health record
- metabolic syndrome
- multiple sclerosis
- big data
- atrial fibrillation
- artificial intelligence
- deep learning
- molecular docking
- insulin resistance
- skeletal muscle
- subarachnoid hemorrhage
- genetic diversity
- cerebral ischemia