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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 {alpha}-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 {alpha}-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 {alpha}-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 {alpha}-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 {alpha}-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 {alpha}-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 {alpha}-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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