Background In 2017, more than 5 million house structures were sprayed through the U.S. President’s Malaria Initiative, protecting more than 21 million people in sub-Saharan Africa. New IRS formulations, SumiShield™ 50WG and Fludora Fusion™ WP-SB, became World Health Organization (WHO) prequalified vector control products in 2017 and 2018, respectively. Both formulations contain the neonicotinoid active ingredient, clothianidin. The target site of neonicotinoids represents a novel mode of action for vector control, meaning that cross-resistance through existing mechanisms is less likely. In preparation for rollout of clothianidin formulations as part of national IRS rotation strategies, baseline susceptibility testing was conducted in 16 countries in sub-Saharan Africa. Methods While work coordinated by the WHO is ongoing to develop a suitable bottle bioassay procedure, there was no published guidance regarding clothianidin susceptibility procedures or diagnostic concentrations. Therefore, a protocol was developed for impregnating filter papers with 2% w/v SumiShield™ 50WG dissolved in distilled water. Susceptibility tests were conducted using insectary-reared reference Anopheles and wild collected malaria vector species. All tests were conducted within 24 h of treating papers, with mortality recorded daily for 7 days, due to the slow-acting nature of clothianidin against mosquitoes. Anopheles gambiae sensu lato (s.l.) adults from wild collected larvae were tested in 14 countries, with wild collected F 0 Anopheles funestus s.l. tested in Mozambique and Zambia. Results One-hundred percent mortality was reached with all susceptible insectary strains and with wild An. gambiae s.l. from all sites in 11 countries. However, tests in at least one location from 5 countries produced mortality below 98%. While this could potentially be a sign of clothianidin resistance, it is more likely that the diagnostic dose or protocol requires further optimization. Repeat testing in 3 sites in Ghana and Zambia, where possible resistance was detected, subsequently produced 100% mortality. Results showed susceptibility to clothianidin in 38 of the 43 sites in sub-Saharan Africa, including malaria vectors with multiple resistance mechanisms to pyrethroids, carbamates and organophosphates. Conclusions This study provides an interim diagnostic dose of 2% w/v clothianidin on filter papers which can be utilized by National Malaria Control Programmes and research organizations until the WHO concludes multi-centre studies and provides further guidance. Electronic supplementary material The online version of this article (10.1186/s12936-019-2888-6) contains supplementary material, which is available to authorized users.

Malaria is a major cause of morbidity and mortality in children and adults in the Sudano Sahel of Northeastern Nigeria with the highest prevalence of malaria in pregnancy of 64.5 in Nigeria recorded in this region. This study was carried out in 2003 and 2004 to provide parasitological baseline data for the development of Malaria Early Warning System (MEWS) for the surveillance of type I epidemic caused by meteorological conditions and to provide data for timing malaria key vector control measures such as Indoor Residual Spraying (IRS) for maximum effect. Clinical information about malaria cases were used in this study. In all 692 children aged 6 to 96 months were screened for Plasmodium infection and used for the analysis. The results showed that the majority of infected children (68.06%) were aged 12-60 months and their asexual parasite density (ap/ u1) was between 100-500 ap/u1 of the whole blood. The month of September recorded the highest Geometric Mean Asexual-Densities (GMPD) of 13,655 while the lowest parasite densities were observed at the peak of the dry season, especially during the months of March and April. Significance difference (p<0.05) was observed between the sexes in infection rate. It is obvious that male children have higher infection rate (about 67.5%), than while female children (32.5%) regardless of climate seasonality. Designing a malaria early warning system and providing baseline parasitological data for timing of spraying cycles for key malaria vector control measures such as Indoor Residual Spraying (IRS) should be encouraged to complement other effective malaria control strategies. Hence the need for this investigation.

Development of resistance by different malaria vector populations to insecticides has become a big threat to malaria vector elimination. This study evaluated the susceptibility of Anopheles mosquito populations in Akwa Ibom State, Nigeria to permethrin (0.75%), deltamethrin (0.5%), lambdacyhalothrin (0.5%), alphacypermethrin (0.75%), Dichlorodiphenyltrichloethane (DDT), propoxur, bendiocarb and pirimiphosmethylin in World Health Organization (WHO) test tubes following standard protocols. The mosquitoes were obtained as aquatic forms and reared under laboratory conditions to adults. The adults were subjected to WHO susceptibility bioassays following standard procedures. Malaria vectors across the study sites were resistant to permethrin, deltamethrin, lambdacyhalothrin and alphacypermethrin insecticides. Full susceptibility to propoxur and bendiocarb was recorded across the sites. Full susceptibility to pirimiphosmethyl was recorded in populations from three sites. Nevertheless, population of the malaria vectors collected from Oron was resistant to pirimiphosmethyl. KDT50 and KDT95 estimated for each insecticide using a log-time probit model revealed that knockdown was more rapid for deltamethrin, lambdacyhalothrin, alphacypermethrin, propoxur, bendiocarb and pirimiphosmethyl than for DDT and permethrin  across the study sites. Morphological identification of all the mosquito samples used revealed that they were female Anopheles gambiae s.l. Sustained susceptibility of malaria vectors to pyrethriod is necessary for successful malaria control with insecticide treated nets and Indoor Residual Spraying (IRS). Emergence of focal points with insecticide resistance gives serious concern especially with the scale-up in distribution of pyrethriod treated nets to these areas. This may increase selection pressures due to overexposure. Further study to identify the exact resistance mechanism(s) of malaria vectors from these sites is recommended.

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