Department of Bacteriology and Medical Mycology, Istituto Superiore di Sanità, Rome, Italy
Correspondence: Dr. Antonio Cassone, Department of Bacteriology and Medical Mycology, Istituto Superiore di Sanità, Viale Regina Elena, 299, 00161, Rome, Italy. E-mail: cassone{at}iss.it
Hyphae formation from yeast cells is a virulence trait enabling the
human opportunistic pathogen Candida albicans to invade
host tissues. Hyphal cells proved to be much less efficient than yeast
cells in stimulating production of macrophage inflammatory protein-1
(MIP-1
), MIP-1ß, interleukin-8 (IL-8), and particularly, monocyte
chemotactic protein-1 (MCP-1) by human monocyte. This different
stimulation did not depend on the monocyte inability to ingest the
hyphae nor did it imply hyphal resistance to the extracellular killing
by the monocytes. Purified hyphal and yeast cell walls reproduced the
differences shown by the intact cells, and chemical-enzymatic
dissection of cell wall components suggested that cell wall ß-1,6
rather than ß-1,3 glucan was the main chemokine inducer. Coherently,
immunofluorescence studies with an anti ß-1,6 glucan serum showed
that the surface expression of this polysaccharide was much lower on
hyphae than on yeast cells. By minimizing chemokine induction, the
formation of hyphal filaments might facilitate C. albicans
escaping from host immunity.
Key Words: phagocytes macrophage inflammatory protein-1
macrophage inflammatory protein-1ß monocyte chemotactic protein-1 interleukin-8 RANTES
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