The long term objective of the proposed work is to identify naturally occurring mosquito mechanisms that affect the development of Plasmodium falciparum in the vector, Anopheles gambiae, in West Africa. These mechanisms may include vector immune responses as well as variant molecules involved in critical vector-parasite molecular interactions. Understanding these mechanisms will illuminate the biology of the relationship between vector and parasite and could be useful in developing a novel malaria control strategy.
The specific aims are to: 1) Identify the major An. gambiae genetic loci that control susceptibility to P. falciparum in the natural malaria transmission system in Mali, West Africa. A genome-wide scan will be conducted in large pedigrees of wild An. gambiae. Loci will be detected by genetic linkage of midgut oocyst number with a multilocus microsatellite genotype at 10 centiMorgan resolution. 2) Analyze the same mosquito pedigrees to determine the influence of two known refractory mechanisms, encapsulation and lysis, in the natural P. falciparum transmission system, by genetic linkage analysis with microsatellite markers. In addition, a laboratory study will determine the parasite species-specificity of the lysis refractory response of An. gambiae, in which parasites are destroyed within midgut epithelial cells. 3) Determine the association between chromosomal forms of An. gambiae and susceptibility of P. falciparum infection, by cytogenetic analysis of the infected mosquito pedigrees. Natural populations of An. gambiae are subdivided into genetic subgroups based on chromosome inversions. Preliminary evidence suggests the forms may differ in malaria vector competence. Laboratory studies have shown that vector mechanisms with a simple genetic basis can greatly affect the efficiency of parasite development. However, laboratory systems can depart from the biology of natural malaria transmission in important ways. Mechanisms of vector susceptibility to malaria parasites in nature have not been studied. This project will be the first examination of naturally-occurring mechanisms of mosquito refractoriness to malaria parasites in the P. falciparum transmission system.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI042361-03
Application #
6170943
Study Section
Special Emphasis Panel (ZRG5-TMP (01))
Program Officer
Aultman, Kathryn S
Project Start
1998-08-05
Project End
2002-07-31
Budget Start
2000-08-01
Budget End
2001-07-31
Support Year
3
Fiscal Year
2000
Total Cost
$457,155
Indirect Cost
Name
New York University
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
City
New York
State
NY
Country
United States
Zip Code
10016
Redmond, Seth N; Eiglmeier, Karin; Mitri, Christian et al. (2015) Association mapping by pooled sequencing identifies TOLL 11 as a protective factor against Plasmodium falciparum in Anopheles gambiae. BMC Genomics 16:779
Rottschaefer, Susan M; Crawford, Jacob E; Riehle, Michelle M et al. (2015) Population genetics of Anopheles coluzzii immune pathways and genes. G3 (Bethesda) 5:329-39
Jiang, Xiaofang; Peery, Ashley; Hall, A Brantley et al. (2014) Genome analysis of a major urban malaria vector mosquito, Anopheles stephensi. Genome Biol 15:459
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Holm, Inge; Lavazec, Catherine; Garnier, Thierry et al. (2012) Diverged alleles of the Anopheles gambiae leucine-rich repeat gene APL1A display distinct protective profiles against Plasmodium falciparum. PLoS One 7:e52684
Crawford, Jacob E; Bischoff, Emmanuel; Garnier, Thierry et al. (2012) Evidence for population-specific positive selection on immune genes of Anopheles gambiae. G3 (Bethesda) 2:1505-19
Mitri, Christian; Vernick, Kenneth D (2012) Anopheles gambiae pathogen susceptibility: the intersection of genetics, immunity and ecology. Curr Opin Microbiol 15:285-91
Riehle, Michelle M; Guelbeogo, Wamdaogo M; Gneme, Awa et al. (2011) A cryptic subgroup of Anopheles gambiae is highly susceptible to human malaria parasites. Science 331:596-8
Mitri, Christian; Jacques, Jean-Claude; Thiery, Isabelle et al. (2009) Fine pathogen discrimination within the APL1 gene family protects Anopheles gambiae against human and rodent malaria species. PLoS Pathog 5:e1000576
Riehle, Michelle M; Xu, Jiannong; Lazzaro, Brian P et al. (2008) Anopheles gambiae APL1 is a family of variable LRR proteins required for Rel1-mediated protection from the malaria parasite, Plasmodium berghei. PLoS One 3:e3672

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