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Originally published In Press as doi:10.1074/jbc.M206296200 on October 7, 2002

J. Biol. Chem., Vol. 277, Issue 51, 49921-49926, December 20, 2002
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Epithelial Innate Immunity
A NOVEL ANTIMICROBIAL PEPTIDE WITH ANTIPARASITIC ACTIVITY IN THE BLOOD-SUCKING INSECT STOMOXYS CALCITRANS*

Nathalie BoulangerDagger §, Rebecca J. L. Munks§||, Joanne V. Hamilton||, Françoise Vovelle**, Reto BrunDagger Dagger , Mike J. Lehane||, and Philippe BuletDagger

From the Dagger  Institut de Biologie Moléculaire et Cellulaire, 15 Rue René Descartes, 67084 Strasbourg Cedex, France, the || School of Biological Sciences, University of Wales, Bangor LL57 2UW, United Kingdom, the ** Centre de Biophysique Moléculaire, CNRS, Rue Charles Sadron, 45071 Orléans Cedex 2, France, and the Dagger Dagger  Swiss Tropical Institute, P. O. Box, 4002 Basel, Switzerland

The gut epithelium is an essential interface in insects that transmit parasites. We investigated the role that local innate immunity might have on vector competence, taking Stomoxys calcitrans as a model. S. calcitrans is sympatric with tsetse flies, feeds on many of the same vertebrate hosts, and is thus regularly exposed to the trypanosomes that cause African sleeping sickness and nagana. Despite this, S. calcitrans is not a cyclical vector of these trypanosomes. Trypanosomes develop exclusively in the lumen of digestive organs, and so epithelial immune mechanisms, and in particular antimicrobial peptides (AMPs), may be the prime determinants of the fate of an infection. To investigate why S. calcitrans is not a cyclical vector of trypanosomes, we have looked in its midgut for AMPs with trypanolytic activity. We have identified a new AMP of 42 amino acids, which we named stomoxyn, constitutively expressed and secreted exclusively in the anterior midgut of S. calcitrans. It displays an amphipathic helical structure and exhibits a broad activity spectrum affecting the growth of microorganisms. Interestingly, this AMP exhibits trypanolytic activity to Trypanosoma brucei rhodesiense. We argue that stomoxyn may help to explain why S. calcitrans is not a vector of trypanosomes causing African sleeping sickness and nagana.


* This work was supported by grants from the Wellcome Trust, Biotechnology and Biological Sciences Research Council (BBSRC), CNRS, and EntoMed (Strasbourg).The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

The nucleotide sequence(s) reported in this paper has been submitted to the GenBankTM/EBI Data Bank with accession number(s) AF467987

§ These authors contributed equally to this work.

To whom correspondence should be addressed. Tel.: 33-3-90-24-41-51; Fax: 33-3-90-24-43-08; E-mail: nboulanger@aspirine.u-strasbg.fr.


Copyright © 2002 by The American Society for Biochemistry and Molecular Biology, Inc.
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