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Infection and Immunity, December 2003, p. 7061-7068, Vol. 71, No. 12
0019-9567/03/$08.00+0 DOI: 10.1128/IAI.71.12.7061-7068.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.
ß-1,2- and
-1,2-Linked Oligomannosides Mediate Adherence of Candida albicans Blastospores to Human Enterocytes In Vitro
Fredéric Dalle,1,2 Thierry Jouault,3 Pierre André Trinel,3 Jacques Esnault,4 Jean Maurice Mallet,4 Philippe d'Athis,5 Daniel Poulain,3 and Alain Bonnin1,2*
Laboratoire
de Parasitologie Mycologie,1
Service d'Informatique
Médicale et Biostatistique, Hôpital du
Bocage,5
Laboratoire de Microbiologie
Médicale et Moléculaire, Faculté de
Médecine, 21079 Dijon Cedex,2
Laboratoire de
Mycologie Fondamentale et Appliquée, Equipe INSERM 0360,
Faculté de Médecine Pôle Recherche, 59037
Lille Cedex,3
Département de Chimie,
Ecole Normale Supérieure, UMR CNRS 8642, 75231 Paris
Cedex 05, France4
Received 12 May 2003/
Returned for modification 22 June 2003/
Accepted 2 August 2003
Candida
albicans is a commensal dimorphic yeast of the digestive tract
that causes hematogenously disseminated infections in immunocompromised
individuals. Endogenous invasive candidiasis develops from C.
albicans adhering to the intestinal epithelium. Adherence is
mediated by the cell wall surface, a domain composed essentially of
mannopyranosyl residues bound to proteins, the N-linked moiety of which
comprises sequences of
-1,2- and ß-1,2-linked mannose
residues. ß-1,2-linked mannosides are also associated with a
glycolipid, phospholipomannan, at the C. albicans surface. In
order to determine the roles of ß-1,2 and
-1,2
oligomannosides in the C. albicans-enterocyte interaction, we
developed a model of adhesion of C. albicans VW32 blastospores
to the apical regions of differentiated Caco-2 cells. Preincubation of
yeasts with monoclonal antibodies (MAbs) specific for
-1,2 and
ß-1,2 mannan epitopes resulted in a dose-dependent decrease in
adhesion (50% of the control with a 60-µg/ml MAb
concentration). In competitive assays ß-1,2 and
-1,2
tetramannosides were the most potent carbohydrate inhibitors, with
50% inhibitory concentrations of 2.58 and 6.99 mM, respectively.
Immunolocalization on infected monolayers with MAbs specific for
-1,2 and ß-1,2 oligomannosides showed that these
epitopes were shed from the yeast to the enterocyte surface. Taken
together, our data indicate that
-1,2 and ß-1,2
oligomannosides are involved in the C. albicans-enterocyte
interaction and participate in the adhesion of the yeasts to the
mucosal
surface.
* Corresponding
author. Mailing address: Alain Bonnin, Laboratoire de Parasitologie
Mycologie, Hôpital du Bocage, BP 77908, 21079 Dijon Cedex,
France. Phone: 33 (0)380 29 36 03 or 33 (0)380 29 35 23. Fax: 33 (0)380
29 32 80. E-mail:
alain.bonnin{at}chu-dijon.fr.
Editor:
T. R. Kozel
Infection and Immunity, December 2003, p. 7061-7068, Vol. 71, No. 12
0019-9567/03/$08.00+0 DOI: 10.1128/IAI.71.12.7061-7068.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.
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Copyright © 2003 by the American Society for Microbiology. All rights reserved.