» Articles » PMID: 39208072

Dramatic Resurgence of Malaria After 7 Years of Intensive Vector Control Interventions in Eastern Uganda

Abstract

Tororo District, Uganda experienced a dramatic decrease in malaria burden from 2015-19 during 5 years of indoor residual spraying (IRS) with carbamate (Bendiocarb) and then organophosphate (Actellic) insecticides. However, a marked resurgence occurred in 2020, which coincided with a change to a clothianidin-based IRS formulations (Fludora Fusion/SumiShield). To quantify the magnitude of the resurgence, investigate causes, and evaluate the impact of a shift back to IRS with Actellic in 2023, we assessed changes in malaria metrics in regions within and near Tororo District. Malaria surveillance data from Nagongera Health Center, Tororo District was included from 2011-2023. In addition, a cohort of 667 residents from 84 houses was followed from August 2020 through September 2023 from an area bordering Tororo and neighboring Busia District, where IRS has never been implemented. Cohort participants underwent passive surveillance for clinical malaria and active surveillance for parasitemia every 28 days. Mosquitoes were collected in cohort households every 2 weeks using CDC light traps. Female Anopheles were speciated and tested for sporozoites and phenotypic insecticide resistance. Temporal comparisons of malaria metrics were stratified by geographic regions. At Nagongera Health Center average monthly malaria cases varied from 419 prior to implementation of IRS; to 56 after 5 years of IRS with Bendiocarb and Actellic; to 1591 after the change in IRS to Fludora Fusion/SumiShield; to 155 after a change back to Actellic. Among cohort participants living away from the border in Tororo, malaria incidence increased over 8-fold (0.36 vs. 2.97 episodes per person year, p<0.0001) and parasite prevalence increased over 4-fold (17% vs. 70%, p<0.0001) from 2021 to 2022 when Fludora Fusion/SumiShield was used. Incidence decreased almost 5-fold (2.97 vs. 0.70, p<0.0001) and prevalence decreased by 39% (70% vs. 43%, p<0.0001) after shifting back to Actellic. There was a similar pattern among those living near the border in Tororo, with increased incidence between 2021 and 2022 (0.93 vs. 2.40, p<0.0001) followed by a decrease after the change to Actellic (2.40 vs. 1.33, p<0.001). Among residents of Busia, malaria incidence did not change significantly over the 3 years of observation. Malaria resurgence in Tororo was temporally correlated with the replacement of An. gambiae s.s. by An. funestus as the primary vector, with a marked decrease in the density of An. funestus following the shift back to IRS with Actellic. In Busia, An. gambiae s.s. remained the primary vector throughout the observation period. Sporozoite rates were approximately 50% higher among An. funestus compared to the other common malaria vectors. Insecticide resistance phenotyping of An. funestus revealed high tolerance to clothianidin, but full susceptibility to Actellic. A dramatic resurgence of malaria in Tororo was temporally associated with a change to clothianidin-based IRS formulations and emergence of An. funestus as the predominant vector. Malaria decreased after a shift back to IRS with Actellic. This study highlights the ability of malaria vectors to rapidly circumvent control efforts and the importance of high-quality surveillance systems to assess the impact of malaria control interventions and generate timely, actionable data.

Citing Articles

Significant variations in tolerance to clothianidin and pirimiphos-methyl in and populations during a dramatic malaria resurgence despite sustained indoor residual spraying in Uganda.

Oruni A, Arinaitwe E, Adiga J, Otto G, Kyagamba P, Okoth J bioRxiv. 2025; .

PMID: 40027642 PMC: 11870430. DOI: 10.1101/2025.02.13.638152.


Relating household entomological measures to individual malaria risk.

McClure M, Arinaitwe E, Kamya M, Rosenthal P, Nankabirwa J, Maxwell K Res Sq. 2025; .

PMID: 39975909 PMC: 11838747. DOI: 10.21203/rs.3.rs-5914493/v1.


Epidemiology, clinical spectrum, and outcomes of severe malaria in Eastern Uganda: a prospective study.

Namayanja C, Paasi G, Alunyo J, Amorut D, Okalebo C, Okiror W Malar J. 2025; 24(1):37.

PMID: 39920795 PMC: 11806871. DOI: 10.1186/s12936-024-05221-5.


Temporal evolution of insecticide resistance and bionomics in Anopheles funestus, a key malaria vector in Uganda.

Oruni A, Tchouakui M, Tagne C, Hearn J, Kayondo J, Wondji C Sci Rep. 2024; 14(1):32027.

PMID: 39738472 PMC: 11685729. DOI: 10.1038/s41598-024-83689-6.

References
1.
Mzilahowa T, Chiumia M, Mbewe R, Uzalili V, Luka-Banda M, Kutengule A . Increasing insecticide resistance in Anopheles funestus and Anopheles arabiensis in Malawi, 2011-2015. Malar J. 2016; 15(1):563. PMC: 5120501. DOI: 10.1186/s12936-016-1610-1. View

2.
Wirtz R, DUNCAN J, Njelesani E, Schneider I, Brown A, Oster C . ELISA method for detecting Plasmodium falciparum circumsporozoite antibody. Bull World Health Organ. 1989; 67(5):535-42. PMC: 2491279. View

3.
Djouaka R, Riveron J, Yessoufou A, Tchigossou G, Akoton R, Irving H . Multiple insecticide resistance in an infected population of the malaria vector Anopheles funestus in Benin. Parasit Vectors. 2016; 9:453. PMC: 4987972. DOI: 10.1186/s13071-016-1723-y. View

4.
Raouf S, Mpimbaza A, Kigozi R, Sserwanga A, Rubahika D, Katamba H . Resurgence of Malaria Following Discontinuation of Indoor Residual Spraying of Insecticide in an Area of Uganda With Previously High-Transmission Intensity. Clin Infect Dis. 2017; 65(3):453-460. PMC: 5850037. DOI: 10.1093/cid/cix251. View

5.
Nankabirwa J, Rek J, Arinaitwe E, Namuganga J, Nsobya S, Asua V . East Africa International Center of Excellence for Malaria Research: Summary of Key Research Findings. Am J Trop Med Hyg. 2022; 107(4_Suppl):21-32. PMC: 9662228. DOI: 10.4269/ajtmh.21-1285. View