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Table 1 Studies evaluating Anopheles mosquito mortality and Plasmodium transmission after imbibing blood containing ivermectin

From: Ivermectin to reduce malaria transmission: a research agenda for a promising new tool for elimination

Reference

Methods

Species

Results

Pampiglione 1985 [24]

Feeding on impregnated cotton and on treated mice.

An. stephensi

Increased mortality in all groups feeding on impregnated cotton, 100% mortality in those feeding at 28,000 μg/L.

Dose: 140–28,000 μg/kg (once, subcutaneous)

 

100% mortality 24-hr post feeding on mice treated at dose ≥2,800 μg/kg. Increased mortality in all other dose-groups.

Iakubovich 1989 [25]

Membrane and feeding on treated rabbits.

Dose: 340 μg/kg (once, subcutaneous)

An. stephensi

Death rates among An. stephensi fed on rabbits 4, 5 and 6 days after administration of the drug were 93, 70 and 79%, respectively.

 

An. atroparvus

No difference with control seen in An. sacharovi and An. atroparvus.

 

An. sacharovi

 

Jones 1992 [26]

Membrane and feeding on treated dogs

Dose: 10–2,500 μg/kg (once, orally)

An. quadrimaculatus

Mortality ≥90% in all but one treatment groups 24-hr post blood feeding and ≥90% in all groups 48-hr post blood feeding

Gardner 1993 [27]

Feeding on treated dogs

An. quadrimaculatus

Significant increase in mortality. LD50 = 9.9 μg/kg [6.0, 13.8]

Dose: 6–24 μg/kg (once, orally)

 

Significant decrease in oviposition and egg-hatching from survivors

Bockarie 1999 [21]

Field collections of engorged females before and after MDA for lymphatic filariasis

An. punctulatus

Significant decrease in 9-day cumulative survival rate of Anopheles spp. collected 1–3 days post-treatment (0%) vs those collected pre-treatment (67%)

Dose: 400 μg/kg ivermectin +/- 6 mg/kg DEC (once, orally)

An. koliensis

The 48-hr survival rate of An. puctulatus collected from two houses in the a treated village the morning following MDA was 31% vs 94% from two houses of an untreated village

  

Pre- and post-treatment all-night landing catches showed no significant reduction in human biting rates.

Foley 2000 [20]

Feeding on one treated human volunteer

Dose: 250 μg/kg (once, orally)

An. farauti

12-day cumulative mortality rate of mosquitoes was 100%, 95%, 93%, and 40% for those fed 0, 7, 10 and 14 days post-treatment vs 10% for those fed pre-treatment

Fritz 2009 [28]

Membrane and feeding on treated cattle

An. gambiae

Membrane feeding: LC50 for An. gambiae s.l. was 19.8 ± 2.8 ppb; no oviposition from mosquitoes fed on >10 ppb

 

Dose: 600 μg/kg (once, subcutaneously)

An. arabiensis

Cattle feeding: Total cumulative survival of An. gambiae s.s. significantly different from controls when fed up to 20 days post-treatment; no or significantly reduced oviposition when fed up to 17 days post-treatment

Chaccour 2010 [19]

Feeding on randomized, treated volunteers and controls

 

Mean 12-day survival time of 2.38 days [1.52, 3.24] for mosquitoes fed on treated subjects at 1 day post-treatment vs 5.52 days [4.65, 6.4] for mosquitoes fed on untreated control subjects

Dose: 200 μg/kg (once, orally)

An. gambiae

No effect on mosquitoes fed on treated subjects at 14 days post-treatment

Kobylinski 2010 [16]

membrane feedings

Dose: NA

An. gambiae

LC50 = 22.4 ng/ml [18.0, 26.9]. At sub-lethal concentrations, significantly reduced mosquito re-blood feeding rates and a second ivermectin blood meal, even at a decreased concentration, further increased mortality

Sylla 2010 [23]

Field collections of engorged females before and after MDA for onchocerciasis

An. gambiae

5-day cumulative survival of An. gambiae s.s. was significantly reduced from 3 treated villages vs pair-matched control villages

Dose: 150 μg/kg (once, orally)

An. arabiensis

An. gambiae s.s. captured in treated villages 1–6 days post-treatment had significantly reduced survival v those caught pre-MDA and those caught >7 days post-treatment

Kobylinski 2011 [22]

Field collections of engorged females before and after MDA for onchocerciasis

An. gambiae

For 12 days after the MDA, mean P. falciparum sporozoite rate was significantly reduced by 79% in 3 replicate treated villages while it increased by 246% in pair-matched control villages

 

Dose: 150 μg/kg (once, orally)

  

Butters 2012 [29]

Membrane feeding

Dose: NA

An. gambiae

Sub-lethal concentrations (LC25 & LC5) caused significant knockdown and reduced recovery rates

Fritz 2012 [30]

Membrane feeding

Dose: NA

An. arabiensis

LC50 = 7 · 9 ppb [6.2, 9.9]; oviposition among survivors was significantly reduced at ≥7 ppb

Bastiaens 2012 [31]

Feeding on treated Swiss mice, Wistar rats and Cynomolgus monkeys

Dose: 200–400 μg/kg (different intervals, orally)

An. stephensi

3-day cumulative mortality of mosquitoes fed on treated mice, rats and monkeys significantly differed from controls when fed up to 2, 4 and 3 days post-treatment, respectively

Kobylinski 2012 [32]

Membrane feeding

An. gambiae

Sub-lethal concentrations significantly inhibited P. falciparum sporogony when fed prior to, concurrent with, and 6 and 9 days after infection with gametocytes

 

Dose: NA

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