Literature DB >> 10432066

Short report: entomologic inoculation rates and Plasmodium falciparum malaria prevalence in Africa.

J C Beier1, G F Killeen, J I Githure.   

Abstract

Epidemiologic patterns of malaria infection are governed by environmental parameters that regulate vector populations of Anopheles mosquitoes. The intensity of malaria parasite transmission is normally expressed as the entomologic inoculation rate (EIR), the product of the vector biting rate times the proportion of mosquitoes infected with sporozoite-stage malaria parasites. Malaria transmission intensity in Africa is highly variable with annual EIRs ranging from < 1 to > 1,000 infective bites per person per year. Malaria control programs often seek to reduce morbidity and mortality due to malaria by reducing or eliminating malaria parasite transmission by mosquitoes. This report evaluates data from 31 sites throughout Africa to establish fundamental relationships between annual EIRs and the prevalence of Plasmodium falciparum malaria infection. The majority of sites fitted a linear relationship (r2 = 0.71) between malaria prevalence and the logarithm of the annual EIR. Some sites with EIRs < 5 infective bites per year had levels of P. falciparum prevalence exceeding 40%. When transmission exceeded 15 infective bites per year, there were no sites with prevalence rates < 50%. Annual EIRs of 200 or greater were consistently associated with prevalence rates > 80%. The basic relationship between EIR and P. falciparum prevalence, which likely holds in east and west Africa, and across different ecologic zones, shows convincingly that substantial reductions in malaria prevalence are likely to be achieved only when EIRs are reduced to levels less than 1 infective bite per person per year. The analysis also highlights that the EIR is a more direct measure of transmission intensity than traditional measures of malaria prevalence or hospital-based measures of infection or disease incidence. As such, malaria field programs need to consider both entomologic and clinical assessments of the efficacy of transmission control measures.

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Year:  1999        PMID: 10432066     DOI: 10.4269/ajtmh.1999.61.109

Source DB:  PubMed          Journal:  Am J Trop Med Hyg        ISSN: 0002-9637            Impact factor:   2.345


  154 in total

1.  The potential impact of integrated malaria transmission control on entomologic inoculation rate in highly endemic areas.

Authors:  G F Killeen; F E McKenzie; B D Foy; C Schieffelin; P F Billingsley; J C Beier
Journal:  Am J Trop Med Hyg       Date:  2000-05       Impact factor: 2.345

2.  Force of infection is key to understanding the epidemiology of Plasmodium falciparum malaria in Papua New Guinean children.

Authors:  Ivo Mueller; Sonja Schoepflin; Thomas A Smith; Kathryn L Benton; Michael T Bretscher; Enmoore Lin; Benson Kiniboro; Peter A Zimmerman; Terence P Speed; Peter Siba; Ingrid Felger
Journal:  Proc Natl Acad Sci U S A       Date:  2012-06-04       Impact factor: 11.205

3.  A biologic basis for integrated malaria control.

Authors:  F Ellis McKenzie; J Kevin Baird; John C Beier; Altaf A Lal; William H Bossert
Journal:  Am J Trop Med Hyg       Date:  2002-12       Impact factor: 2.345

4.  Intermittent preventive treatment for malaria in infants: a decision-support tool for sub-Saharan Africa.

Authors:  Ilona Carneiro; Lucy Smith; Amanda Ross; Arantxa Roca-Feltrer; Brian Greenwood; Joanna Armstrong Schellenberg; Thomas Smith; David Schellenberg
Journal:  Bull World Health Organ       Date:  2010-05-10       Impact factor: 9.408

5.  Malaria transmission and vector behaviour in a forested malaria focus in central Vietnam and the implications for vector control.

Authors:  Wim Van Bortel; Ho Dinh Trung; Le Xuan Hoi; Nguyen Van Ham; Nguyen Van Chut; Nguyen Dinh Luu; Patricia Roelants; Leen Denis; Niko Speybroeck; Umberto D'Alessandro; Marc Coosemans
Journal:  Malar J       Date:  2010-12-23       Impact factor: 2.979

6.  Placental malaria diminishes development of antibody responses to Plasmodium falciparum epitopes in infants residing in an area of western Kenya where P. falciparum is endemic.

Authors:  Phillip Cullison Bonner; Zhiyong Zhou; Lisa B Mirel; John G Ayisi; Ya Ping Shi; Anna M van Eijk; Juliana A Otieno; Bernard L Nahlen; Richard W Steketee; Venkatachalam Udhayakumar
Journal:  Clin Diagn Lab Immunol       Date:  2005-03

7.  Anopheles gambiae s.l. and Anopheles funestus mosquito distributions at 30 villages along the Kenyan coast.

Authors:  Joseph Keating; Charles M Mbogo; Joseph Mwangangi; Joseph G Nzovu; Vweidong Gu; James L Regens; Guiyun Yan; John I Githure; John C Beier
Journal:  J Med Entomol       Date:  2005-05       Impact factor: 2.278

8.  Association between protection against clinical malaria and antibodies to merozoite surface antigens in an area of hyperendemicity in Myanmar: complementarity between responses to merozoite surface protein 3 and the 220-kilodalton glutamate-rich protein.

Authors:  Soe Soe; Michael Theisen; Christian Roussilhon; Khin-Saw Aye; Pierre Druilhe
Journal:  Infect Immun       Date:  2004-01       Impact factor: 3.441

Review 9.  Impact of malaria during pregnancy on low birth weight in sub-Saharan Africa.

Authors:  Helen L Guyatt; Robert W Snow
Journal:  Clin Microbiol Rev       Date:  2004-10       Impact factor: 26.132

10.  Population genetic structure of Plasmodium falciparum in the two main African vectors, Anopheles gambiae and Anopheles funestus.

Authors:  Zeinab Annan; Patrick Durand; Francisco J Ayala; Céline Arnathau; Parfait Awono-Ambene; Frédéric Simard; Fabien G Razakandrainibe; Jacob C Koella; Didier Fontenille; François Renaud
Journal:  Proc Natl Acad Sci U S A       Date:  2007-04-30       Impact factor: 11.205

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