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Efficacy of Actellic 300 CS-based indoor residual spraying on key entomological indicators of malaria transmission in Alibori and Donga, two regions of northern Benin

The current study shows the results of three years of IRS entomological monitoring (2016, before intervention; 2017 and 2018, after intervention) performed in Alibori and Donga, northern Benin. Mosquito collections were performed on a monthly basis using human landing catches and pyrethrum spray cat...

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Published in:Parasites & vectors 2019-12, Vol.12 (1), p.612-612, Article 612
Main Authors: Salako, Albert Sourou, Dagnon, Fortune, Sovi, Arthur, Padonou, Gil Germain, Aïkpon, Rock, Ahogni, Idelphonse, Syme, Thomas, Govoétchan, Renaud, Sagbohan, Herman, Sominahouin, André Aimé, Akinro, Bruno, Iyikirenga, Laurent, Agossa, Fiacre, Akogbeto, Martin Codjo
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container_title Parasites & vectors
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creator Salako, Albert Sourou
Dagnon, Fortune
Sovi, Arthur
Padonou, Gil Germain
Aïkpon, Rock
Ahogni, Idelphonse
Syme, Thomas
Govoétchan, Renaud
Sagbohan, Herman
Sominahouin, André Aimé
Akinro, Bruno
Iyikirenga, Laurent
Agossa, Fiacre
Akogbeto, Martin Codjo
description The current study shows the results of three years of IRS entomological monitoring (2016, before intervention; 2017 and 2018, after intervention) performed in Alibori and Donga, northern Benin. Mosquito collections were performed on a monthly basis using human landing catches and pyrethrum spray catches in six districts including four treated with Actellic 300 CS (Kandi, Gogounou, Djougou and Copargo) and two untreated (Bembèrèkè and Kouandé) which served as control sites. Key transmission indicators of Anopheles gambiae (s.l.) as well as the residual activity of Actellic 300 CS assessed through WHO cone tests, were determined. The residual efficacy duration of Actellic 300 CS after the two IRS campaigns (2017 and 2018) was 4-5 months (May-September). The parity rate and the sporozoite index of An. gambiae (s.l.) were 36.62% and 0.71%, respectively, after the first spray round in treated areas compared to 57.24% and 3.7%, respectively, in the control areas (P 
doi_str_mv 10.1186/s13071-019-3865-1
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Dagnon, Fortune ; Sovi, Arthur ; Padonou, Gil Germain ; Aïkpon, Rock ; Ahogni, Idelphonse ; Syme, Thomas ; Govoétchan, Renaud ; Sagbohan, Herman ; Sominahouin, André Aimé ; Akinro, Bruno ; Iyikirenga, Laurent ; Agossa, Fiacre ; Akogbeto, Martin Codjo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c566t-4455aae23691d6b8b00c2fa71e32073c5977e939fdb6fad4fe3659f3a2da052d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Actellic 300CS</topic><topic>Animals</topic><topic>Anopheles</topic><topic>Anopheles - drug effects</topic><topic>Anopheles - parasitology</topic><topic>Anopheles - physiology</topic><topic>Aquatic insects</topic><topic>Benin</topic><topic>Bioassays</topic><topic>Bites (Injuries)</topic><topic>Collections</topic><topic>Control</topic><topic>Disease transmission</topic><topic>Efficacy</topic><topic>Feeding habits</topic><topic>Female</topic><topic>Human diseases</topic><topic>Humans</topic><topic>Indicators</topic><topic>Inoculation</topic><topic>Insect bites</topic><topic>Insecticides</topic><topic>Insecticides - pharmacology</topic><topic>Intervention</topic><topic>IRS</topic><topic>Malaria</topic><topic>Malaria - parasitology</topic><topic>Malaria - transmission</topic><topic>Mortality</topic><topic>Mosquito Control - instrumentation</topic><topic>Mosquito Control - methods</topic><topic>Mosquito Vectors - drug effects</topic><topic>Mosquito Vectors - parasitology</topic><topic>Mosquito Vectors - physiology</topic><topic>Mosquitoes</topic><topic>Organothiophosphorus Compounds - pharmacology</topic><topic>Parity</topic><topic>Physiology</topic><topic>Plasmodium - genetics</topic><topic>Plasmodium - isolation &amp; 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vectors</jtitle><addtitle>Parasit Vectors</addtitle><date>2019-12-30</date><risdate>2019</risdate><volume>12</volume><issue>1</issue><spage>612</spage><epage>612</epage><pages>612-612</pages><artnum>612</artnum><issn>1756-3305</issn><eissn>1756-3305</eissn><abstract>The current study shows the results of three years of IRS entomological monitoring (2016, before intervention; 2017 and 2018, after intervention) performed in Alibori and Donga, northern Benin. Mosquito collections were performed on a monthly basis using human landing catches and pyrethrum spray catches in six districts including four treated with Actellic 300 CS (Kandi, Gogounou, Djougou and Copargo) and two untreated (Bembèrèkè and Kouandé) which served as control sites. Key transmission indicators of Anopheles gambiae (s.l.) as well as the residual activity of Actellic 300 CS assessed through WHO cone tests, were determined. The residual efficacy duration of Actellic 300 CS after the two IRS campaigns (2017 and 2018) was 4-5 months (May-September). The parity rate and the sporozoite index of An. gambiae (s.l.) were 36.62% and 0.71%, respectively, after the first spray round in treated areas compared to 57.24% and 3.7%, respectively, in the control areas (P &lt; 0.0001). The same trend was observed after the second spray round. After the first spray round, each person received 1.6 infective bites/month (ib/m) in the treated areas against 12.11 ib/m in the control areas, resulting in a reduction rate of 86.78%. Similarly, the entomological inoculation rate was 1.5 ib/m after the second spray round in the treated areas vs 9.75 ib/m in the control areas, corresponding to a reduction of 84.61%. A decrease in the parity rate (46.26%), sporozoite index (85.75%) and EIR (87.27%) was observed for An. gambiae (s.l.) after the first round of IRS (June-October 2017) compared to the pre-intervention period (June-October 2016). The density of An. gambiae (s.l.) ranged between 0.38-0.48 per house in treated areas vs 1.53-1.76 An. gambiae (s.l.) per house respectively after the first and second IRS rounds. This study showed the positive impact of IRS in reducing key entomological parameters of malaria transmission in Alibori and Donga. However, the considerable blood-feeding rate of An. gambiae (s.l.) in spray areas, stress the need for the population to sleep under long-lasting insecticidal nets (LLINs) in addition, to prevent from mosquito bites which did not succeed in resting on sprayed walls.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>31888730</pmid><doi>10.1186/s13071-019-3865-1</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
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ispartof Parasites & vectors, 2019-12, Vol.12 (1), p.612-612, Article 612
issn 1756-3305
1756-3305
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_fb74a809c7db4ab4b0ae62d150af959e
source PubMed Central (Open Access); Publicly Available Content Database
subjects Actellic 300CS
Animals
Anopheles
Anopheles - drug effects
Anopheles - parasitology
Anopheles - physiology
Aquatic insects
Benin
Bioassays
Bites (Injuries)
Collections
Control
Disease transmission
Efficacy
Feeding habits
Female
Human diseases
Humans
Indicators
Inoculation
Insect bites
Insecticides
Insecticides - pharmacology
Intervention
IRS
Malaria
Malaria - parasitology
Malaria - transmission
Mortality
Mosquito Control - instrumentation
Mosquito Control - methods
Mosquito Vectors - drug effects
Mosquito Vectors - parasitology
Mosquito Vectors - physiology
Mosquitoes
Organothiophosphorus Compounds - pharmacology
Parity
Physiology
Plasmodium - genetics
Plasmodium - isolation & purification
Plasmodium - physiology
Reduction
Sleep
Spraying
Vector-borne diseases
title Efficacy of Actellic 300 CS-based indoor residual spraying on key entomological indicators of malaria transmission in Alibori and Donga, two regions of northern Benin
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