This project proposes an in depth analysis of innate immune responses of mosquitoes to nicroorganisms, including medically important pathogens and potential bioterrorism agents. A central goal is to understand the immune responses of parasite-susceptible and refractory strains of Anopheles gambiae, the major vector of human malaria, in particular the responses mounted in different organs of the vector during the complex developmental cycle of the parasite in the mosquito. These studies will use the rodent malaria agent, Plasmodium berghei, as a tractable model system. The work will be aided by recent developments which include: (a) full genome sequencing of A. gambiae, and its bioinformatic comparison with the model genome of Drosophila melanogaster, as reported in Science (issue of October 4, 2002); (b) DNA microarrays for RNA profiling in A. gambiae; (c) an efficient reverse genetic method based on direct injection of double stranded RNA in the adult mosquito, permitting functional inactivation of individual genes in vivo; (d) conditional tissue specific transgenic analysis of in vivo gene function; and (e) protocols for immunolocalization that have already permitted the detection of immune stimulated activation of specific genes in specific tissues and cells in the mosquito. A broader analysis of responses to bacteria will facilitate dissection of immune responses, and will place the anti-parasitic responses in context. Mechanisms of molecular recognition leading to immune responses will be of special interest. This work will be followed by (and will facilitate) carefully targeted studies directed towards characterization of mosquito immune responses to the most important human malaria parasite, P. falciparum, which is a considerably more difficult experimental system than P. bergheL Finally, a comparative bioinformatic study of the immune related gene families in two distantly related mosquitoes, A. gambiae and Aedes aegypti will be performed taking advantage of our earlier Anopheles-Drosophila comparison and an ongoing genomic analysis of Aedes, which is an important Iviral vector. This will set the stage for future experimental analysis of immune responses to Aedes- borne pathogens.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program Projects (P01)
Project #
5P01AI044220-09
Application #
7486238
Study Section
Special Emphasis Panel (ZAI1)
Project Start
Project End
Budget Start
2007-07-01
Budget End
2008-06-30
Support Year
9
Fiscal Year
2007
Total Cost
$295,253
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
073130411
City
Boston
State
MA
Country
United States
Zip Code
02199
Gendrin, Mathilde; Turlure, Fanny; Rodgers, Faye H et al. (2017) The Peptidoglycan Recognition Proteins PGRPLA and PGRPLB Regulate Anopheles Immunity to Bacteria and Affect Infection by Plasmodium. J Innate Immun 9:333-342
Lombardo, Fabrizio; Christophides, George K (2016) Novel factors of Anopheles gambiae haemocyte immune response to Plasmodium berghei infection. Parasit Vectors 9:78
Lombardo, Fabrizio; Ghani, Yasmeen; Kafatos, Fotis C et al. (2013) Comprehensive genetic dissection of the hemocyte immune response in the malaria mosquito Anopheles gambiae. PLoS Pathog 9:e1003145
Cezairliyan, Brent; Vinayavekhin, Nawaporn; Grenfell-Lee, Daniel et al. (2013) Identification of Pseudomonas aeruginosa phenazines that kill Caenorhabditis elegans. PLoS Pathog 9:e1003101
Feinbaum, Rhonda L; Urbach, Jonathan M; Liberati, Nicole T et al. (2012) Genome-wide identification of Pseudomonas aeruginosa virulence-related genes using a Caenorhabditis elegans infection model. PLoS Pathog 8:e1002813
Chung, Yoon-Suk Alexander; Kocks, Christine (2012) Phagocytosis of bacterial pathogens. Fly (Austin) 6:21-5
Whiteman, Noah K; Gloss, Andrew D; Sackton, Timothy B et al. (2012) Genes involved in the evolution of herbivory by a leaf-mining, Drosophilid fly. Genome Biol Evol 4:900-16
Pukkila-Worley, Read; Ausubel, Frederick M (2012) Immune defense mechanisms in the Caenorhabditis elegans intestinal epithelium. Curr Opin Immunol 24:3-9
Chung, Yoon-Suk Alexander; Kocks, Christine (2011) Recognition of pathogenic microbes by the Drosophila phagocytic pattern recognition receptor Eater. J Biol Chem 286:26524-32
Limmer, Stefanie; Haller, Samantha; Drenkard, Eliana et al. (2011) Pseudomonas aeruginosa RhlR is required to neutralize the cellular immune response in a Drosophila melanogaster oral infection model. Proc Natl Acad Sci U S A 108:17378-83

Showing the most recent 10 out of 88 publications