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Impact of Vector Control Interventions on Malaria Transmission Intensity, Outdoor Vector Biting Rates and Anopheles Mosquito Species Composition in Tororo, Uganda

Overview
Journal Malar J
Publisher Biomed Central
Specialty Tropical Medicine
Date 2019 Dec 29
PMID 31881898
Citations 52
Authors
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Abstract

Background: Long-lasting insecticidal nets (LLINs) and indoor residual spraying of insecticide (IRS) are widely recommended for the prevention of malaria in endemic regions. Data from human landing catches provide information on the impact of vector control on vector populations. Here, malaria transmission indoors and outdoors, before and after mass deployment of LLINs and IRS in Uganda was compared.

Methods: The study took place in Tororo district, a historically high transmission area where universal LLIN distribution was conducted in November 2013 and May 2017 and 6 rounds of IRS implemented from December 2014 to July 2018. Human landing catches were performed in 8 houses monthly from October 2011 to September 2012 (pre-intervention period) and every 4 weeks from November 2017 to October 2018 (post-intervention period). Mosquitoes were collected outdoors from 18:00 to 22:00 h and indoors from 18:00 to 06:00 h. Female Anopheles were tested for the presence of Plasmodium falciparum sporozoites and species identification performed using gross dissection and polymerase chain reaction (PCR).

Results: The interventions were associated with a decline in human biting rate from 19.6 to 2.3 female Anopheles mosquitoes per house per night (p < 0.001) and annual entomological inoculation rate from 129 to 0 infective bites per person per year (p < 0.001). The proportion of mosquitoes collected outdoors increased from 11.6 to 49.4% (p < 0.001). Prior to the interventions the predominant species was Anopheles gambiae sensu stricto (s.s.), which comprised an estimated 76.7% of mosquitoes. Following the interventions, the predominant species was Anopheles arabiensis, which comprised 99.5% of mosquitoes, with almost complete elimination of An. gambiae s.s. (0.5%).

Conclusions: Mass distribution of LLINs and 6 rounds of IRS dramatically decreased vector density and sporozoite rate resulting in a marked reduction in malaria transmission intensity in a historically high transmission site in Uganda. These changes were accompanied by a shift in vector species from An. gambiae s.s. to An. arabiensis and a relative increase in outdoor biting.

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References
1.
Abduselam N, Zeynudin A, Berens-Riha N, Seyoum D, Pritsch M, Tibebu H . Similar trends of susceptibility in Anopheles arabiensis and Anopheles pharoensis to Plasmodium vivax infection in Ethiopia. Parasit Vectors. 2016; 9(1):552. PMC: 5069880. DOI: 10.1186/s13071-016-1839-0. View

2.
Mawejje H, Wilding C, Rippon E, Hughes A, Weetman D, Donnelly M . Insecticide resistance monitoring of field-collected Anopheles gambiae s.l. populations from Jinja, eastern Uganda, identifies high levels of pyrethroid resistance. Med Vet Entomol. 2012; 27(3):276-83. PMC: 3543752. DOI: 10.1111/j.1365-2915.2012.01055.x. View

3.
Alegana V, Kigozi S, Nankabirwa J, Arinaitwe E, Kigozi R, Mawejje H . Spatio-temporal analysis of malaria vector density from baseline through intervention in a high transmission setting. Parasit Vectors. 2016; 9(1):637. PMC: 5153881. DOI: 10.1186/s13071-016-1917-3. View

4.
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

5.
Mendis C, Jacobsen J, Bule E, Dgedge M, Thompson R, Cuamba N . Anopheles arabiensis and An. funestus are equally important vectors of malaria in Matola coastal suburb of Maputo, southern Mozambique. Med Vet Entomol. 2000; 14(2):171-80. DOI: 10.1046/j.1365-2915.2000.00228.x. View