TY - JOUR
T1 - Shifts in malaria vector species composition and transmission dynamics along the Kenyan coast over the past 20 years
AU - Mwangangi, Joseph M.
AU - Mbogo, Charles M.
AU - Orindi, Benedict O.
AU - Muturi, Ephantus J.
AU - Midega, Janet T.
AU - Nzovu, Joseph
AU - Gatakaa, Hellen
AU - Githure, John
AU - Borgemeister, Christian
AU - Keating, Joseph
AU - Beier, John C.
N1 - Funding Information:
We are grateful for the assistance of all scientific staff at the Kenya Medical Research Institute, Centre for Geographic Medicine Research-Coast, particularly Dr Norbert Peshu and Professor Kevin Marsh. We are grateful for critical reviews from Dr Margaret Mackinnon and Dr Phillip Bejon of KEMRI-Wellcome Trust Research Program Kilifi. We thank the technical and field staff for the collection and processing of the mosquitoes, particularly Pamela Seda, Festus Yaah, Shida David, and Gabriel Nzai. We appreciate the effort made by Rosemary Wamae in data entry and retrieval of archived entomological data. This paper is published with the permission of the Director of the Kenya Medical Research Institute. This study was supported by core funds from the International Centre of Insect Physiology and Ecology (icipe), Biovision Foundation, Switzerland grant through icipe (BV-HH-02(B3127A), and by the National Institute of Allergy and Infectious Diseases of the National Institutes of Health under award number U19 AI-45511. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
PY - 2013
Y1 - 2013
N2 - Background: Over the past 20 years, numerous studies have investigated the ecology and behaviour of malaria vectors and Plasmodium falciparum malaria transmission on the coast of Kenya. Substantial progress has been made to control vector populations and reduce high malaria prevalence and severe disease. The goal of this paper was to examine trends over the past 20 years in Anopheles species composition, density, blood-feeding behaviour, and P. falciparum sporozoite transmission along the coast of Kenya. Methods. Using data collected from 1990 to 2010, vector density, species composition, blood-feeding patterns, and malaria transmission intensity was examined along the Kenyan coast. Mosquitoes were identified to species, based on morphological characteristics and DNA extracted from Anopheles gambiae for amplification. Using negative binomial generalized estimating equations, mosquito abundance over the period were modelled while adjusting for season. A multiple logistic regression model was used to analyse the sporozoite rates. Results: Results show that in some areas along the Kenyan coast, Anopheles arabiensis and Anopheles merus have replaced An. gambiae sensu stricto (s.s.) and Anopheles funestus as the major mosquito species. Further, there has been a shift from human to animal feeding for both An. gambiae sensu lato (s.l.) (99% to 16%) and An. funestus (100% to 3%), and P. falciparum sporozoite rates have significantly declined over the last 20 years, with the lowest sporozoite rates being observed in 2007 (0.19%) and 2008 (0.34%). There has been, on average, a significant reduction in the abundance of An. gambiae s.l. over the years (IRR = 0.94, 95% CI 0.90-0.98), with the density standing at low levels of an average 0.006 mosquitoes/house in the year 2010. Conclusion: Reductions in the densities of the major malaria vectors and a shift from human to animal feeding have contributed to the decreased burden of malaria along the Kenyan coast. Vector species composition remains heterogeneous but in many areas An. arabiensis has replaced An. gambiae as the major malaria vector. This has important implications for malaria epidemiology and control given that this vector predominately rests and feeds on humans outdoors. Strategies for vector control need to continue focusing on tools for protecting residents inside houses but additionally employ outdoor control tools because these are essential for further reducing the levels of malaria transmission.
AB - Background: Over the past 20 years, numerous studies have investigated the ecology and behaviour of malaria vectors and Plasmodium falciparum malaria transmission on the coast of Kenya. Substantial progress has been made to control vector populations and reduce high malaria prevalence and severe disease. The goal of this paper was to examine trends over the past 20 years in Anopheles species composition, density, blood-feeding behaviour, and P. falciparum sporozoite transmission along the coast of Kenya. Methods. Using data collected from 1990 to 2010, vector density, species composition, blood-feeding patterns, and malaria transmission intensity was examined along the Kenyan coast. Mosquitoes were identified to species, based on morphological characteristics and DNA extracted from Anopheles gambiae for amplification. Using negative binomial generalized estimating equations, mosquito abundance over the period were modelled while adjusting for season. A multiple logistic regression model was used to analyse the sporozoite rates. Results: Results show that in some areas along the Kenyan coast, Anopheles arabiensis and Anopheles merus have replaced An. gambiae sensu stricto (s.s.) and Anopheles funestus as the major mosquito species. Further, there has been a shift from human to animal feeding for both An. gambiae sensu lato (s.l.) (99% to 16%) and An. funestus (100% to 3%), and P. falciparum sporozoite rates have significantly declined over the last 20 years, with the lowest sporozoite rates being observed in 2007 (0.19%) and 2008 (0.34%). There has been, on average, a significant reduction in the abundance of An. gambiae s.l. over the years (IRR = 0.94, 95% CI 0.90-0.98), with the density standing at low levels of an average 0.006 mosquitoes/house in the year 2010. Conclusion: Reductions in the densities of the major malaria vectors and a shift from human to animal feeding have contributed to the decreased burden of malaria along the Kenyan coast. Vector species composition remains heterogeneous but in many areas An. arabiensis has replaced An. gambiae as the major malaria vector. This has important implications for malaria epidemiology and control given that this vector predominately rests and feeds on humans outdoors. Strategies for vector control need to continue focusing on tools for protecting residents inside houses but additionally employ outdoor control tools because these are essential for further reducing the levels of malaria transmission.
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U2 - 10.1186/1475-2875-12-13
DO - 10.1186/1475-2875-12-13
M3 - Article
C2 - 23297732
AN - SCOPUS:84872004270
SN - 1475-2875
VL - 12
JO - Malaria Journal
JF - Malaria Journal
IS - 1
M1 - 13
ER -