Abstract

BackgroundMedicinal plants are a validated source for discovery of new leads and standardized herbal medicines. The aim of this study was to assess the activity of Vernoniaamygdalina leaf extracts and isolated compounds against gametocytes and sporogonic stages of Plasmodiumberghei and to validate the findings on field isolates of Plasmodium falciparum.MethodsAqueous (Ver-H2O) and ethanolic (Ver-EtOH) leaf extracts were tested in vivo for activity against sexual and asexual blood stage P. berghei parasites. In vivo transmission blocking effects of Ver-EtOH and Ver-H2O were estimated by assessing P. berghei oocyst prevalence and density in Anopheles stephensi mosquitoes. Activity targeting early sporogonic stages (ESS), namely gametes, zygotes and ookinetes was assessed in vitro using P. berghei CTRPp.GFP strain. Bioassay guided fractionation was performed to characterize V.amygdalina fractions and molecules for anti-ESS activity. Fractions active against ESS of the murine parasite were tested for ex vivo transmission blocking activity on P.falciparum field isolates. Cytotoxic effects of extracts and isolated compounds vernolide and vernodalol were evaluated on the human cell lines HCT116 and EA.hy926.ResultsVer-H2O reduced the P. berghei macrogametocyte density in mice by about 50% and Ver-EtOH reduced P. berghei oocyst prevalence and density by 27 and 90%, respectively, in An.stephensi mosquitoes. Ver-EtOH inhibited almost completely (>90%) ESS development in vitro at 50 μg/mL. At this concentration, four fractions obtained from the ethylacetate phase of the methanol extract displayed inhibitory activity >90% against ESS. Three tested fractions were also found active against field isolates of the human parasite P. falciparum, reducing oocyst prevalence in Anopheles coluzzii mosquitoes to one-half and oocyst density to one-fourth of controls. The molecules and fractions displayed considerable cytotoxicity on the two tested cell-lines.ConclusionsVernonia amygdalina leaves contain molecules affecting multiple stages of Plasmodium, evidencing its potential for drug discovery. Chemical modification of the identified hit molecules, in particular vernodalol, could generate a library of druggable sesquiterpene lactones. The development of a multistage phytomedicine designed as preventive treatment to complement existing malaria control tools appears a challenging but feasible goal.Electronic supplementary materialThe online version of this article (doi:10.1186/s12936-015-0812-2) contains supplementary material, which is available to authorized users.

Highlights

  • Medicinal plants are a validated source for discovery of new leads and standardized herbal medicines

  • Examining the same slides of the two experiments for asexual forms, Ver-EtOH was found to reduce parasitaemia by 59.2%

  • Ver-H2O reduced parasitaemia by 33.6%, parasitaemia values of 5.8 and 8.7% were recorded in the treatment and control groups, respectively (p < 0.05)

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Summary

Introduction

Medicinal plants are a validated source for discovery of new leads and standardized herbal medicines. Among the drugs currently used for malaria case management, artemisinin based combination therapy (ACT) [3] and primaquine [4] have impact on malaria transmission, by reducing the infectiousness of individuals to mosquitoes [5]. On the basis of the drugs’ respective activity profiles, the World Health Organization (WHO) recommends the addition of a single dose of primaquine to the ACT course for the management of uncomplicated Plasmodium falciparum malaria in areas threatened by artemisinin resistance and/or in pre-elimination phase [7]. Among the various available approaches, the exploration of empirically effective and chemically characterized anti-malarial plants represents a valid strategy for the discovery of new druggable compounds active against gametocytes and/ or sporogonic stages for the development of multi-stage combination medicines

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