Abstract

Visceral Leishmaniasis (VL) due to Leishmania donovani is a neglected protozoan parasitic disease in humans, which is usually fatal if untreated. Phlebotomus orientalis, the predominant VL vector in East Africa, is a highly exophilic/exophagic species that poses a major challenge to current Integrated Vector Management (IVM). Here we report results of pilot studies conducted in rural villages in Gedarif state, Sudan, to evaluate outdoor residual spraying of 20mg active ingredient (a.i.) /m2 deltamethrin insecticide applied to the characteristic household compound boundary reed fence and to the outside of household buildings (Outdoor Residual Insecticide Spraying, ODRS), and as an alternative, spraying restricted to the boundary fence only (Restricted Outdoor Residual Insecticide Spraying, RODRS). Four to six clusters of 20 households were assigned to insecticide treatments or control in three experiments. Changes in sand fly numbers were monitored over 2,033 trap-nights over 43-76 days follow-up in four sentinel houses per cluster relative to unsprayed control clusters. Sand fly numbers were monitored by sticky traps placed on the ground on the inside ("outdoor") and the outside ("peridomestic") of the boundary fence, and by CDC light traps suspended outdoors in the household compound. The effects of ODRS on sand fly numbers inside sleeping huts were monitored by insecticide knockdown. After a single application, ODRS reduced P. orientalis abundance by 83%-99% in outdoor and peridomestic trap locations. ODRS also reduced numbers of P. orientalis found resting inside sleeping huts. RODRS reduced outdoor and peridomestic P. orientalis by 60%-88%. By direct comparison, RODRS was 58%-100% as effective as ODRS depending on the trapping method. These impacts were immediate on intervention and persisted during follow-up, representing a large fraction of the P. orientalis activity season. Relative costs of ODRS and RODRS delivery were $5.76 and $3.48 per household, respectively. The study demonstrates the feasibility and high entomological efficacy of ODRS and RODRS, and the expected low costs relative to current IVM practises. These methods represent novel sand fly vector control tools against predominantly exophilic/exophagic sand fly vectors, aimed to lower VL burdens in Sudan, with potential application in other endemic regions in East Africa.

Highlights

  • Standard methods to combat hematophagous arthropod vectors of infectious diseases include–among other possibilities- indoor residual spraying of insecticides (IRS) and use of insecticide-treated bednets (ITNs), the success of which largely rely on insecticide-susceptible vector populations showing endophilic and/or endophagic blood-feeding behaviours

  • The marked exophagic and exophilic behaviours of P. orientalis represent a profound challenge for Visceral Leishmaniasis (VL) control by excluding indoor residual spraying of insecticides (IRS) and compromising the efficacy of insecticide-impregnated bednets (ITNs)

  • We evaluated the entomological efficacy of residual pyrethroid applied outdoors to household boundary fences and the exterior walls of household huts, to reduce the abundance of P. orientalis inside and outside houses

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Summary

Introduction

Standard methods to combat hematophagous arthropod vectors of infectious diseases include–among other possibilities- indoor residual spraying of insecticides (IRS) and use of insecticide-treated bednets (ITNs), the success of which largely rely on insecticide-susceptible vector populations showing endophilic and/or endophagic blood-feeding behaviours. [1,2,3] One such challenge includes the Phlebotomine sand fly vectors of the protozoan parasites Leishmania causing human visceral leishmaniasis (VL, known as kala azar) which occurs in East Africa, the Indian sub-continent, the Americas, the Mediterranean region, and Central and Eastern Asia. Africa with some of the highest case incidences worldwide, resulting in severe epidemics in the region [4,5,6,7,8,9,10,11,12], and exerting tremendous social and economic burdens on afflicted populations [13,14]. VL is usually fatal within two years if not treated, and there is no human vaccine

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