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Infection and Immunity, August 2007, p. 4012-4019, Vol. 75, No. 8
0019-9567/07/$08.00+0     doi:10.1128/IAI.00645-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Induction of Nitric Oxide Synthase and Activation of Signaling Proteins in Anopheles Mosquitoes by the Malaria Pigment, Hemozoin{triangledown}

Leyla Akman-Anderson,1 Martin Olivier,2 and Shirley Luckhart1*

Department of Medical Microbiology and Immunology, School of Medicine, University of California at Davis, One Shields Avenue, Davis, California 95616,1 Department of Microbiology and Immunology, McGill University, Lyman Duff Medical Building, 3775 University Street, Montreal, QC H3A 2B4, Canada2

Received 8 May 2007/ Returned for modification 14 May 2007/ Accepted 19 May 2007

Anopheles stephensi, a major vector for malaria parasite transmission, responds to Plasmodium infection by synthesis of inflammatory levels of nitric oxide (NO), which can limit parasite development in the midgut. We have previously shown that Plasmodium falciparum glycosylphosphatidylinositols (PfGPIs) can induce A. stephensi NO synthase (AsNOS) expression in the midgut epithelium in vivo in a manner similar to the manner in which cytokines and NO are induced by PfGPIs in mammalian cells. In mosquito cells, signaling by PfGPIs and P. falciparum merozoites is mediated through Akt/protein kinase B (Akt/PKB), the mitogen-activated protein kinase kinase DSOR1, and extracellular signal-regulated kinase (ERK). In mammalian cells, a second parasite factor, malaria pigment or hemozoin (Hz), signals NOS induction through ERK- and nuclear factor kappa B-dependent pathways and has been demonstrated to be a novel proinflammatory ligand for Toll-like receptor 9. In this study, we demonstrate that Hz can also induce AsNOS gene expression in immortalized A. stephensi and Anopheles gambiae cell lines in vitro and in A. stephensi midgut tissue in vivo. In mosquito cells, Hz signaling is mediated through transforming growth factor ß-associated kinase 1, Akt/PKB, ERK, and atypical protein kinase C zeta/lambda. Our results show that Hz is a prominent parasite-derived signal for Anopheles and that signaling pathways activated by PfGPIs and Hz have both unique and shared components. Together with our previous findings, our data indicate that parasite signaling of innate immunity is conserved in mosquito and mammalian cells.

* Corresponding author. Mailing address: Department of Medical Microbiology and Immunology, 3437 Tupper Hall, One Shields Avenue, School of Medicine, University of California at Davis, Davis, CA 95616. Phone: (530) 754-6963. Fax: (530) 752-8692. E-mail: sluckhart{at}ucdavis.edu

{triangledown} Published ahead of print on 25 May 2007.

Editor: W. A. Petri, Jr.

Infection and Immunity, August 2007, p. 4012-4019, Vol. 75, No. 8
0019-9567/07/$08.00+0     doi:10.1128/IAI.00645-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.



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