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Secretomes of medically important fungi reflect morphological and phylogenetic diversity
Sarai Varona1, José L Lavín1, José A Oguiza2
1Bioinformatics Unit, CIC BioGUNE-BRTA, Bizkaia Technology Park, 48160, Derio, Bizkaia, Spain.
Abstract:
Secretome represents a main target for understanding the mechanisms of fungal adaptation. In the present study, we focus on the secretomes of fungi associated with infections in humans and other mammals in order to explore relationships between the diverse morphological and phylogenetic groups. Almost all the mammalian pathogenic fungi analyzed have secretome sizes smaller than 1000 proteins and, secreted proteins comprise between 5% and 10% of the total proteome. As expected, the correlation pattern between the secretome size and the total proteome was similar to that described in previous secretome studies of fungi. With regard to the morphological groups, minimum secretome sizes of less than 250 secreted proteins and low values for the fraction of secreted proteins are shown in mammalian pathogenic fungi with reduced proteomes such as microsporidia, atypical fungi and some species of yeasts and yeast-like fungi (Malassezia). On the other hand, filamentous fungi have significantly more secreted proteins and the highest numbers are present in species of filamentous fungi that also are plant or insect pathogens (Fusarium verticilloides, Fusarium oxysporum and Basidiobolus meristosporus). With respect to phylogeny, there are also variations in secretome size across fungal subphyla: Microsporidia, Taphrinomycotina, Ustilagomycotina and Saccharomycotina contain small secretomes; whereas larger secretomes are found in Agaricomycotina, Pezizomycotina, Mucoromycotina and Entomophthoromycotina. Finally, principal component analysis (PCA) was conducted on the complete secretomes. The PCA results revealed that, in general, secretomes of fungi belonging to the same morphological group or subphyla cluster together. In conclusion, our results point out that in medically important fungi there is a relationship between the secretome and the morphological group or phylogenetic classification.
Insights
Fungal secretomes, crucial for adaptation, show size variations linked to morphology and phylogeny in mammalian pathogens. These findings reveal patterns connecting fungal secretomes to their classification and evolutionary groups.
Area of Science:
- Mycology
- Fungal Pathogenesis
- Proteomics
Background:
- The secretome, comprising secreted proteins, is vital for understanding fungal adaptation and host interactions.
- Fungal secretomes play a critical role in pathogenicity and survival mechanisms.
Purpose of the Study:
- To investigate the relationships between secretome size and composition across diverse morphological and phylogenetic groups of fungi.
- To explore how secretome characteristics correlate with fungal adaptation in mammalian pathogens.
Main Methods:
- Analysis of secretome sizes and proteome fractions in various mammalian pathogenic fungi.
- Comparative analysis based on morphological groups (yeasts, filamentous fungi) and phylogenetic subphyla.
- Principal Component Analysis (PCA) to identify clustering patterns within secretomes.
Main Results:
- Mammalian pathogenic fungi generally have smaller secretomes (<1000 proteins), with secreted proteins constituting 5-10% of the total proteome.
- Microsporidia, atypical yeasts, and yeast-like fungi exhibit smaller secretomes compared to filamentous fungi.
- Filamentous fungi, particularly those also pathogenic to plants or insects, possess larger secretomes.
- PCA revealed that fungi within the same morphological group or phylogenetic subphyla tend to cluster together based on their secretomes.
Conclusions:
- Fungal secretome size and composition are significantly influenced by morphological and phylogenetic classifications.
- These findings highlight a conserved relationship between secretome characteristics and fungal taxonomy in medically important species.
- Understanding these relationships can provide insights into fungal adaptation and pathogenicity mechanisms.
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