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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
Epithelial Innate Immunity
A NOVEL ANTIMICROBIAL PEPTIDE WITH ANTIPARASITIC ACTIVITY IN THE
BLOOD-SUCKING INSECT STOMOXYS CALCITRANS*
Nathalie
Boulanger §¶,
Rebecca J. L.
Munks§ ,
Joanne V.
Hamilton ,
Françoise
Vovelle**,
Reto
Brun ,
Mike J.
Lehane , and
Philippe
Bulet
From the 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
 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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Copyright © 2002 by the American Society for Biochemistry and Molecular Biology.
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