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Tanzania Journal of Health Research
Health User's Trust Fund (HRUTF)
ISSN: 1821-6404
Vol. 19, No. 3, 2017, pp. 1-10
Bioline Code: th17029
Full paper language: English
Document type: Research Article
Document available free of charge

Tanzania Journal of Health Research, Vol. 19, No. 3, 2017, pp. 1-10

 en Characterization of malaria vectors in Huye District, Southern Rwanda
NYIRAKANANI, CHANTAL; CHIBVONGODZE, RAYMOND; KARIUKI, LENSON; HABTU, MICHAEL; MASIKA, MOSES; MUKOKO, DUNSTAN & NJUNWA, KATO J.

Abstract

Background: Effective control of malaria requires knowledge of vector species, their feeding and resting behaviour as well as breeding habitats. The objective of this study was to determine malaria vector species abundance and identify their larval habitats in Huye district, southern Rwanda.
Methods: Adult mosquitoes were collected indoors using light trap and pyrethrum spray catch techniques, and outdoors using light traps. Female Anopheles check for this species in other resources mosquitoes were identified to species level by morphological characteristics. Enzyme-linked Immunosorbent Assay (ELISA) was used to screen for Plasmodium falciparum circumsporozoite protein and host blood meal sources. Anopheles larvae were sampled using dippers and raised into adult mosquitoes which were identified morphologically.
Results: Anopheles gambiae check for this species in other resources sensu lato comprised of 70% of the 567 Anopheles collected. Other Anopheles species identified were An. funestus check for this species in other resources 4%, An. squamosus check for this species in other resources 16.5%, An. maculipalpis check for this species in other resources 6.5%, An. ziemanni check for this species in other resources 1.7%, An. pharoensis check for this species in other resources 1.2 % and An. coustani check for this species in other resources 0.1%. The majority, 63.5% of the collected mosquitoes were from indoors collections. The overall human blood index was 0.509. The P. falciparum circumsporozoite protein was found in 11 mosquitos including 8 Anopheles gambiae s.l. and 3 secondary vectors out of the 567 tested. The overall sporozoite rate was 1.9%. A total of 661 Anopheline larvae from 22 larval habitats were collected. They comprised of An. gambiae s.l. (89%) and An. ziemanni (11%). The absolute breeding index was 86.4%. The most common larval habitats were in full sunlight with still water like rice paddies and pools of stagnant water.
Conclusion: These findings show that Anopheles gambiae s.l. is the dominant malaria vector in the area with other vectors playing a secondary role in malaria transmission. Malaria interventions need to be strengthened to reduce even further the malaria transmission in the area.

Keywords
malaria; mosquito; composition; larval habitats; Rwanda

 
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