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Am. J. Trop. Med. Hyg., 68(4 suppl), 2003, pp. 115-120
Copyright © 2003 by The American Society of Tropical Medicine and Hygiene

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EFFECT OF PERMETHRIN-TREATED BED NETS ON THE SPATIAL DISTRIBUTION OF MALARIA VECTORS IN WESTERN KENYA

JOHN E. GIMNIG, MARGARETTE S. KOLCZAK, ALLEN W. HIGHTOWER, JOHN M. VULULE, ERIK SCHOUTE, LUNA KAMAU, PENELOPE A. PHILLIPS-HOWARD, FEIKO O. TER KUILE, BERNARD L. NAHLEN, AND WILLIAM A. HAWLEY
Division of Parasitic Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia; Centre for Vector Biology and Control Research, Kenya Medical Research Institute, Kisumu, Kenya; Centre for Biotechnology Research and Development, Kenya Medical Research Institute, Nairobi, Kenya

The effect of insecticide (permethrin)-treated bed nets (ITNs) on the spatial distribution of malaria vectors in neighboring villages lacking ITNs was studied during a randomized controlled trial of ITNs in western Kenya. There was a trend of decreased abundance of Anopheles gambiae with decreasing distance from intervention villages both before (P = 0.027) and after (P = 0.002) introduction of ITNs, but this trend was significantly stronger after ITNs were introduced (P = 0.05). For An. funestus, no pre-intervention trend was observed (P = 0.373), but after the intervention, a trend of decreased abundance with closer proximity to intervention compounds developed (P = 0.027). Reduction in mosquito populations in villages lacking ITNs was most apparent in compounds located within 600 meters of intervention villages. Sporozoite infection rates decreased in control areas following the introduction of ITNs (P < 0.001 for both species), but no spatial association was detected between sporozoite rates and distance to nearest intervention village. We conclude that high coverage of ITNs is associated with a community-wide suppression of mosquito populations that is detectable in neighboring villages lacking ITNs, thereby affording individuals residing in these villages some protection against malaria.


Acknowledgments: We thank Maurice Ombok for coordinating the GPS mapping of the study area and George Olang for organizing the mosquito collections. We also thank Joseph Nduati and George Ojwang for conducting the sporozoite ELISA and for PCR identification of An. gambiae s.l. We also are grateful the residents of Asembo Bay for their support and cooperation throughout the study. This paper has been published with the permission of the director of the Kenya Medical Research Institute.

Financial support: The ITN project was funded by the United States Agency for International Development.

Disclaimer: The opinions or assertions contained in this manuscript are the private ones of the authors and are not to be construed as official or reflecting the views of the U.S. Public Health Service or Department of Health and Human Services. Use of trade names is for identification only and does not imply endorsement by the U.S. Public Health Service or Department of Health and Human Services.

Authors’ addresses: John E. Gimnig, Margarette S. Kolczak, Allen W. Hightower, Penelope A. Phillips-Howard, Feiko O. ter Kuile, and William A. Hawley, Division of Parasitic Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Mailstop F-22, 4770 Buford Highway, Atlanta, GA 30341. John M. Vulule and Erik Schoute, Centre for Vector Biology and Control Research, Kenya Medical Research Institute, PO Box 1578, Kisumu, Kenya. Luna Kamau, Centre for Biotechnology Research and Development, Kenya Medical Research Institute, PO Box 54840, Nairobi, Kenya. Bernard L. Nahlen, Roll Back Malaria, World Health Organization, Avenue Appia 20, 1211 Geneva 27, Switzerland World Health Organization, CH-1211 Geneva 27, Switzerland.




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Copyright © 2003 by the American Society of Tropical Medicine and Hygiene.