Cladophialophora carrionii is one of the four major etiologic
agents of human chromoblastomycosis in semi-arid climates. This species was
studied using sequence data of the internal transcribed spacer region of rDNA,
the partial β-tubulin gene and an intron in the translation elongation
factor 1-alpha gene, in addition to morphology. With all genes a clear
bipartition was observed, which corresponded with minute differences in
conidiophore morphology. A new species, C. yegresii, was introduced,
which appeared to be, in contrast to C. carrionii, associated with
living cactus plants. All strains from humans, and a few isolates from dead
cactus debris, belonged to C. carrionii, for which a lectotype was
designated. Artificial inoculation of cactus plants grown from seeds in the
greenhouse showed that both fungi are able to persist in cactus tissue. When
reaching the spines they produce cells that morphologically resemble the
muriform cells known as the “invasive form” in
chromoblastomycosis. The tested clinical strain of C. carrionii
proved to be more virulent in cactus than the environmental strain of C.
yegresii that originated from the same species of cactus, Stenocereus
griseus. The muriform cell expressed in cactus spines can be regarded as
the extremotolerant survival phase, and is likely to play an essential role in
the natural life cycle of these organisms.
Data are presented on the clinically relevant black yeasts and their relatives, i.e., members of the Ascomycete order Chaetothyriales. In order to understand the pathology of these fungi it is essential to know their natural ecological niche. From a relatively low degree of molecular variability of the black yeast Exophiala dermatitidis, potential agent of brain infections in patients from East Asia, it is concluded that this species is an emerging pathogen, currently going through a process of active speciation. It is found to be an oligotrophic fungus in hot, moist environments, such as steambaths. Cladophialophora-, Fonsecaea- and Ramichloridium-like strains, known in humans as agents of chromoblastomycosis, are frequently found on rotten plant material, but the fungal molecular diversity in the environment is much higher than that on the human patient, so that it is difficult to trace the etiological agents of the disease with precision. This approach has been successful with Cladophialophora carrionii, of which cells resembling muriform cells, the tissue form of chromoblastomycosis, were found to occur in drying spines of cacti. Phagocytosis assays provide a method to distinguish between pathogens and non-pathogens, as the killing rates of strict saprobes proved to be consistently higher than of those species frequently known as agents of disease. The therapeutic possibilities for patients with chromoblastomycosis are reviewed.
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