: Female mosquitoes must blood feed for oogenesis. The blood meal provides iron, but also allows infection and transmission of pathogens by these disease vectors. Mechanisms that allow females to adapt to the iron load in the presence of infectious agents are not known. We have found that mosquitos express iron regulatory protein 1 (IRP1) and the ferritin heavy (HCH) and light chain subunits. Like mammals, mosquito IRP 1 interacts with an iron regulatory element (IRE) found in the HCH mRNA and represses translation. In contrast to mammals, mosquitos secrete ferritin composed of the HCH subunits in response to an iron challenge. Our hypothesis is that mosquitoes avoid cellular iron overload by secreting ferritin and that the HCH is essential for this process and for cell survival. In mammals, ferritin expression is increased in response to infection and H chain expression up regulates expression of some immune factors. We have found that IRP1/IRE interaction is increased as part of the mosquito immune response. We think this reflects phosphorylation of IRP 1. We hypothesize that IRP 1 interaction with the HCH mRNA down regulates ferritin synthesis and compromises vector immunity. We propose the following specific aims to test our hypotheses: (1) To determine the importance of ferritin secretion and each subunit to mosquito survival following an iron challenge, (2) To characterize the effects of infection on IRP 1/IRE interaction and ferritin synthesis in vectors, and (3) To further characterize the mechanism(s) modulating IRP 1/IRE interaction and to obtain other messages that are controlled by IRP1/IRE interaction in mosquitoes. In the longer term, we want to determine how female mosquitoes adapt to an iron load in the presence of infectious agents and whether differences exist in this process between refractory and non-refractory mosquitoes. We also are interested in designing control strategies that modulate IRP1/IRE interaction or that interfere with ferritin synthesis or secretion. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM056812-08
Application #
7088730
Study Section
Special Emphasis Panel (ZRG1-TMP (99))
Program Officer
Shapiro, Bert I
Project Start
1998-08-15
Project End
2008-06-30
Budget Start
2006-07-01
Budget End
2007-06-30
Support Year
8
Fiscal Year
2006
Total Cost
$223,472
Indirect Cost
Name
University of Arizona
Department
Nutrition
Type
Schools of Earth Sciences/Natur
DUNS #
806345617
City
Tucson
State
AZ
Country
United States
Zip Code
85721
Geiser, Dawn L; Zhou, Guoli; Mayo, Jonathan J et al. (2013) The effect of bacterial challenge on ferritin regulation in the yellow fever mosquito, Aedes aegypti. Insect Sci 20:601-19
Pham, Daphne Q D; Winzerling, Joy J (2010) Insect ferritins: Typical or atypical? Biochim Biophys Acta 1800:824-33
Geiser, Dawn L; Shen, Meng-Chieh; Mayo, Jonathan J et al. (2009) Iron loaded ferritin secretion and inhibition by CI-976 in Aedes aegypti larval cells. Comp Biochem Physiol B Biochem Mol Biol 152:352-63
Zhou, Guoli; Velasquez, Lissette S; Geiser, Dawn L et al. (2009) Differential regulation of transferrin 1 and 2 in Aedes aegypti. Insect Biochem Mol Biol 39:234-44
Zhou, Guoli; Kohlhepp, Pete; Geiser, Dawn et al. (2007) Fate of blood meal iron in mosquitoes. J Insect Physiol 53:1169-78