Effect of Consecutive Alternating Administration of a Triple Combination of Anti-Enteroviral Compounds in Mice Infected with Coxsackievirus B3

Pathog Dis. 2020 Nov 23;78(9):ftaa065. doi: 10.1093/femspd/ftaa065.

Abstract

A novel approach for treatment of enterovirus infections was characterized. Application of treatment course of consecutive alternating administration (CAA) of triple combination of enterovirus replication inhibitors in experimental infections (20 MLD50) with coxsackievirus B3 (CVB3) strains in newborn mice is presented. It was established that in infection with cardiotropic Woodruff strain the combination of pleconaril, МDL-860 and oxoglaucine (PMO) subjected to the CAA scheme, a significant protective effect was observed. Monotherapeutic courses as well as simultaneously daily applied PMO were without effect. Analogous data were observed at experimental infection with the neurotriopic Nancy strain of CVB3. Following IC50 values of virus samples taken every day from target organs of infected animals during the whole period of study, a drug-resistance was established in monotherapy with compounds-partners in the PMO combination. At courses by the treatment scheme CAA of PMO development of drug-resistance was not established, but an increased susceptibility to the effect of the inhibitor-components in the combination was proven. Toxicity of PMO applied via the CAA scheme and in the monotherapeutic courses in both healthy and CVB3 infected animals was recorded. All data obtained prove the potential of the CAA treatment scheme for development of effective chemotherapy of enterovirus infections.

Keywords: CVB3; MDL-860; drug susceptibility; mice; oxoglaucine; pleconaril.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antiviral Agents / pharmacology
  • Apomorphine / analogs & derivatives*
  • Apomorphine / pharmacology
  • Cell Line
  • Coxsackievirus Infections / drug therapy*
  • Coxsackievirus Infections / virology
  • Disease Models, Animal
  • Drug Resistance, Viral
  • Drug Synergism
  • Drug Therapy, Combination
  • Enterovirus B, Human / drug effects*
  • Enterovirus B, Human / physiology
  • Humans
  • Mice
  • Nitriles / pharmacology*
  • Oxadiazoles / pharmacology*
  • Oxazoles / pharmacology*
  • Virus Replication / drug effects

Substances

  • Antiviral Agents
  • Nitriles
  • Oxadiazoles
  • Oxazoles
  • oxoglaucine
  • 2-(3,4-dichlorophenoxy)-5-nitrobenzonitrile
  • pleconaril
  • Apomorphine