Nationwide insecticide resistance status and biting behaviour of malaria vector species in the Democratic Republic of Congo

Globally, the Democratic Republic of Congo (DRC) accounted for 9% of malaria cases and 10% of malaria deaths in 2015. As part of control efforts, more than 40 million long-lasting insecticidal nets (LLINs) were distributed between 2008 and 2013, resulting in 70% of households owning one or more LLIN...

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Published in:	Malaria journal Vol. 17; no. 1; p. 129
Main Authors:	Wat'senga, Francis, Manzambi, Emile Zola, Lunkula, Andre, Mulumbu, Roger, Mampangulu, Tania, Lobo, Neil, Hendershot, Allison, Fornadel, Christen, Jacob, Djenam, Niang, Mame, Ntoya, Ferdinand, Muyembe, Tamfum, Likwela, Joris, Irish, Seth R, Oxborough, Richard M
Format:	Journal Article
Language:	English
Published:	England BioMed Central 27-03-2018 BMC
Subjects:	Animals Anopheles - drug effects Anopheles - physiology Democratic Republic of the Congo Feeding Behavior Insect Bites and Stings - etiology Insecticide Resistance Insecticides - pharmacology Malaria Mosquito Vectors - drug effects Mosquito Vectors - physiology Nitriles - pharmacology Permethrin - pharmacology Pyrethrins - pharmacology Democratic Republic of the Congo
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Summary:	Globally, the Democratic Republic of Congo (DRC) accounted for 9% of malaria cases and 10% of malaria deaths in 2015. As part of control efforts, more than 40 million long-lasting insecticidal nets (LLINs) were distributed between 2008 and 2013, resulting in 70% of households owning one or more LLINs in 2014. To optimize vector control efforts, it is critical to monitor vector behaviour and insecticide resistance trends. Entomological data was collected from eight sentinel sites throughout DRC between 2013 and 2016 in Kingasani, Mikalayi, Lodja, Kabondo, Katana, Kapolowe, Tshikaji and Kalemie. Mosquito species present, relative densities and biting times were monitored using human landing catches (HLC) conducted in eight houses, three times per year. HLC was conducted monthly in Lodja and Kapolowe during 2016 to assess seasonal dynamics. Laboratory data included resistance mechanism frequency and sporozoite rates. Insecticide susceptibility testing was conducted with commonly used insecticides including deltamethrin and permethrin. Synergist bioassays were conducted with PBO to determine the role of oxidases in permethrin resistance. In Lodja, monthly Anopheles gambiae s.l. biting rates were consistently high at > 10 bites/person/night indoors and outdoors. In Kapolowe, An. gambiae s.l. dominated during the rainy season, and Anopheles funestus s.l. during the dry season. In all sites, An. gambiae and An. funestus biting occurred mostly late at night. In Kapolowe, significant biting of both species started around 19:00, typically before householders use nets. Sporozoite rates were high, with a mean of 4.3% (95% CI 3.4-5.2) for An. gambiae and 3.3% (95% CI 1.3-5.3) for An. funestus. Anopheles gambiae were resistant to permethrin in six out of seven sites in 2016. In three sites, susceptibility to deltamethrin was observed despite high frequency permethrin resistance, indicating the presence of pyrethroid-specific resistance mechanisms. Pre-exposure to PBO increased absolute permethrin-associated mortality by 24%, indicating that resistance was partly due to metabolic mechanisms. The kdr-1014F mutation in An. gambiae was present at high frequency (> 70%) in three sites (Kabondo, Kingasani and Tshikaji), and lower frequency (< 20%) in two sites (Lodja and Kapolowe). The finding of widespread resistance to permethrin in DRC is concerning and alternative insecticides should be evaluated.
Bibliography:	ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23
ISSN:	1475-2875 1475-2875
DOI:	10.1186/s12936-018-2285-6