Ivermectin inhibits the sporogony of Plasmodium falciparum in Anopheles gambiae

Abstract Background When ingested in a blood meal, ivermectin has been shown to reduce the survivorship of Anopheles gambiae in the laboratory and field. Furthermore, ivermectin mass drug administrations in Senegal have been shown to reduce the proportion of Plasmodium falciparum -sporozoite-contain...

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Bibliographic Details
Published in:Malaria Journal
Main Authors: Kobylinski Kevin C, Foy Brian D, Richardson Jason H
Format: Article in Journal/Newspaper
Language:English
Published: BMC 2012
Subjects:
Online Access:https://doi.org/10.1186/1475-2875-11-381
https://doaj.org/article/6fabc9a9e30d4191a783bf3014e46405
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Summary:Abstract Background When ingested in a blood meal, ivermectin has been shown to reduce the survivorship of Anopheles gambiae in the laboratory and field. Furthermore, ivermectin mass drug administrations in Senegal have been shown to reduce the proportion of Plasmodium falciparum -sporozoite-containing An. gambiae . This study addresses whether ivermectin inhibits sporogony of P. falciparum in An. gambiae. Methods Anophele gambiae s.s. G3 strain were fed two concentrations of ivermectin (LC 25 and LC 5 ) along with P. falciparum NF54 in human blood meals at staggered intervals. Mosquitoes ingested ivermectin concurrent with parasites (DPI 0), or at three (DPI 3), six (DPI 6), and nine (DPI 9) days post parasite ingestion, or three days prior (DPI −3) to parasite ingestion. Mosquitoes were dissected at seven, twelve or fourteen days post parasite ingestion and either oocyst or sporozoite prevalence was recorded. To determine if P. falciparum sporozoite-containing An. gambiae were more susceptible to ivermectin than uninfected controls, survivorship was recorded for mosquitoes which ingested P. falciparum or control blood meal on DPI 0 and then a second blood meal containing ivermectin (LC 25 ) on DPI 14. Results Ivermectin (LC 25 ) co-ingested (DPI 0) with parasites reduced the proportion of An. gambiae that developed oocysts ( χ 2 = 15.4842, P = 0.0002) and sporozoites ( χ 2 = 19.9643, P < 0.0001). Ivermectin (LC 25 ) ingested DPI 6 ( χ 2 = 8.5103, P = 0.0044) and 9 ( χ 2 = 14.7998, P < 0.0001) reduced the proportion of An. gambiae that developed sporozoites but not when ingested DPI 3 ( χ 2 = 0.0113, P = 1). Ivermectin (LC 5 ) co-ingested (DPI 0) with parasites did not reduce the proportion of An. gambiae that developed oocysts ( χ 2 = 4.2518, P = 0.0577) or sporozoites ( χ 2 = 2.3636, P = 0.1540), however, when ingested DPI −3 the proportion of An. gambiae that developed sporozoites was reduced ( χ 2 = 8.4806, P = 0.0047). Plasmodium falciparum infection significantly reduced the survivorship of An. ...