Abstract

BackgroundThe wide use of gametocytocidal artemisinin-based combination therapy (ACT) lead to a reduction of Plasmodium falciparum transmission in several African endemic settings. An increased impact on malaria burden may be achieved through the development of improved transmission-blocking formulations, including molecules complementing the gametocytocidal effects of artemisinin derivatives and/or acting on Plasmodium stages developing in the vector. Azadirachtin, a limonoid (tetranortriterpenoid) abundant in neem (Azadirachta indica, Meliaceae) seeds, is a promising candidate, inhibiting Plasmodium exflagellation in vitro at low concentrations. This work aimed at assessing the transmission-blocking potential of NeemAzal®, an azadirachtin-enriched extract of neem seeds, using the rodent malaria in vivo model Plasmodium berghei/Anopheles stephensi.MethodsAnopheles stephensi females were offered a blood-meal on P. berghei infected, gametocytaemic BALB/c mice, treated intraperitoneally with NeemAzal, one hour before feeding. The transmission-blocking activity of the product was evaluated by assessing oocyst prevalence, oocyst density and capacity to infect healthy mice. To characterize the anti-plasmodial effects of NeemAzal® on early midgut stages, i.e. zygotes and ookinetes, Giemsa-stained mosquito midgut smears were examined.ResultsNeemAzal® completely blocked P. berghei development in the vector, at an azadirachtin dose of 50 mg/kg mouse body weight. The totally 138 examined, treated mosquitoes (three experimental replications) did not reveal any oocyst and none of the healthy mice exposed to their bites developed parasitaemia. The examination of midgut content smears revealed a reduced number of zygotes and post-zygotic forms and the absence of mature ookinetes in treated mosquitoes. Post-zygotic forms showed several morphological alterations, compatible with the hypothesis of an azadirachtin interference with the functionality of the microtubule organizing centres and with the assembly of cytoskeletal microtubules, which are both fundamental processes in Plasmodium gametogenesis and ookinete formation.ConclusionsThis work demonstrated in vivo transmission blocking activity of an azadirachtin-enriched neem seed extract at an azadirachtin dose compatible with 'druggability' requisites. These results and evidence of anti-plasmodial activity of neem products accumulated over the last years encourage to convey neem compounds into the drug discovery & development pipeline and to evaluate their potential for the design of novel or improved transmission-blocking remedies.

Highlights

  • The wide use of gametocytocidal artemisinin-based combination therapy (ACT) lead to a reduction of Plasmodium falciparum transmission in several African endemic settings

  • In the last decade, a renewed commitment to the fight against malaria has arisen from governments of endemic countries and international organizations, with the explicit aim to eliminate the disease in low transmission settings and to reduce its burden in high transmission areas through high coverage application of insecticide treated mosquito nets and artemisinin-based combination therapy (ACT) [1]

  • Block of the sporogonic development The development of P. berghei in An. stephensi mosquitoes was blocked when the sexual stages of the parasite were ingested by females taking a blood meal on NAtreated, gametocytaemic mice

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Summary

Introduction

The wide use of gametocytocidal artemisinin-based combination therapy (ACT) lead to a reduction of Plasmodium falciparum transmission in several African endemic settings. A renewed commitment to the fight against malaria has arisen from governments of endemic countries and international organizations, with the explicit aim to eliminate the disease in low transmission settings and to reduce its burden in high transmission areas through high coverage application of insecticide treated mosquito nets and artemisinin-based combination therapy (ACT) [1]. There is evidence that the stress imposed to parasites by drug treatment determines an up-regulation in the production of sexual stages [4] These observations imply that treating patients with schizonticidal drugs has the unwanted detrimental ‘side effect’, from a public health perspective, of favouring the transmission of the parasite, jeopardising malaria control efforts at community level. It has been demonstrated that the use of ACT can counteract the spread of parasite strains already resistant to one of the partner drugs [5]

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