Effect of amphotericin B on the infection success of Schistosoma mansoni in Biomphalaria glabrata

Exp Parasitol. 2010 Jun;125(2):70-5. doi: 10.1016/j.exppara.2009.12.024. Epub 2010 Jan 11.

Abstract

In the present study, we examined the effect of amphotericin B on larval stages (miracidia and primary sporocyst) of the helminth Schistosoma mansoni, the causative agent of human schistosomiasis. Amphotericin B (AmB) is a polyene macrolide that disturbs the function of the cell membrane; it is widely used as prophylactic antimycotic agent in in vitro culture. We show for the first time that S. mansoni miracidia infectivity is considerably reduced after AmB treatment. Moreover we demonstrate that AmB does not affect the development, growth, viability, and behavior of miracidia and primary sporocysts. Our data indicate that AmB effects on S. mansoni sporocyst prevalence are linked to the oxidative properties of AmB. These may alter the capacity of sporocysts to respond to the oxidative stress generated by the snail immune defence system.

MeSH terms

  • Amebicides / pharmacology*
  • Amphotericin B / pharmacology*
  • Animals
  • Anti-Bacterial Agents / pharmacology
  • Antioxidants / metabolism
  • Biomphalaria / parasitology*
  • Cricetinae
  • Hemocytes / drug effects
  • Hemocytes / metabolism
  • Movement / drug effects
  • Oocysts / drug effects
  • Oocysts / growth & development
  • Oocysts / metabolism
  • Oxidative Stress
  • Penicillin G / pharmacology
  • Reactive Oxygen Species / metabolism
  • Schistosoma mansoni / drug effects*
  • Schistosoma mansoni / metabolism
  • Schistosoma mansoni / physiology
  • Streptomycin / pharmacology

Substances

  • Amebicides
  • Anti-Bacterial Agents
  • Antioxidants
  • Reactive Oxygen Species
  • Amphotericin B
  • Penicillin G
  • Streptomycin