Nitric oxide-releasing prodrug for the treatment of complex Mycobacterium abscessus infections.
Rebecca A McDonaldSarah G NagyMadyson ChambersChris A BrobergMona J R AhonenMark H SchoenfischPublished in: Antimicrobial agents and chemotherapy (2024)
Non-tuberculosis mycobacteria (NTM) can cause severe respiratory infection in patients with underlying pulmonary conditions, and these infections are extremely difficult to treat. In this report, we evaluate a nitric oxide (NO)-releasing prodrug [methyl tris diazeniumdiolate (MD3)] against a panel of NTM clinical isolates and as a treatment for acute and chronic NTM infections in vivo . Its efficacy in inhibiting growth or killing mycobacteria was explored in vitro alongside evaluation of the impact to primary human airway epithelial tissue. Airway epithelial tissues remained viable after exposure at concentrations of MD3 needed to kill mycobacteria, with no inherent toxic effect from drug scaffold after NO liberation. Resistance studies conducted via serial passage with representative Mycobacterium abscessus isolates demonstrated no resistance to MD3. When administered directly into the lung via intra-tracheal administration in mice, MD3 demonstrated significant reduction in M. abscessus bacterial load in both acute and chronic models of M. abscessus lung infection. In summary, MD3 is a promising treatment for complex NTM pulmonary infection, specifically those caused by M. abscessus , and warrants further exploration as a therapeutic.
Keyphrases
- nitric oxide
- molecular dynamics
- mycobacterium tuberculosis
- liver failure
- pulmonary hypertension
- signaling pathway
- endothelial cells
- gene expression
- emergency department
- hydrogen peroxide
- cancer therapy
- intensive care unit
- respiratory failure
- hepatitis c virus
- cross sectional
- metabolic syndrome
- pulmonary tuberculosis
- nitric oxide synthase
- induced pluripotent stem cells
- hiv aids
- extracorporeal membrane oxygenation
- hiv infected
- respiratory tract
- case control