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Biomaterial‐Associated Infection with Candida albicans in Mice
Author(s) -
Różalska Barbara,
Ljungh Asa,
Burow Aleksandra,
Rudnicka Wiesława
Publication year - 1995
Publication title -
microbiology and immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.664
H-Index - 70
eISSN - 1348-0421
pISSN - 0385-5600
DOI - 10.1111/j.1348-0421.1995.tb02227.x
Subject(s) - candida albicans , microbiology and biotechnology , corpus albicans , biology , peritonitis , fibronectin , adhesion , phagocytosis , cell , immunology , biochemistry , chemistry , genetics , organic chemistry
Abstract Candida yeasts are frequently isolated from patients with continuous ambulatory peritoneal dialysis peritonitis or other biomaterial‐associated infections. The mouse model of candidal peritonitis was used to study the interaction of Candida cells with end‐point attached heparinized polyethylene (H‐PE) and with polymorphonuclear leukocytes (PMNs) or macrophages (Mφ). Two Candida strains differing in cell surface hydrophobicity and in expression of fibronectin (Fn) binding were used for the study. Cells of both Candida strains adhered at higher numbers to H‐PE surfaces preadsorbed with Fn or with human dialysis fluid (HDF) than to non‐modified H‐PE, supporting a role of Fn in mediating adhesion. C. albicans 4016 cells expressing low hydrophobicity and low binding of soluble Fn demonstrated stronger adhesion to PMNs than the more hydrophobic C. albicans 3248 yeasts, which express high binding of soluble Fn. However, C. albicans 4016 cells were more resistant to phagocytic killing and were hardly eradicated in intraperitoneally infected mice. The animals depleted in PMNs by treatment with CY were neither able to eradicate C. albicans 3248 (rapidly eliminated by normal mice) nor C. albicans 4016 yeasts (with a tendency to persist in the tissues of normal mice).