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Published on: March 29, 2012
The 'species complex' issue in clinically relevant fungi: A case study in Scedosporium apiospermum
Min Chen1, Jingsi Zeng2, G Sybren De Hoog3
1Shanghai Institute of Medical Mycology, Shanghai Key Laboratory of Molecular Medical Mycology, Department of Dermatology, Shanghai Changzheng Hospital, Shanghai 200003, China; CBS-KNAW Fungal Biodiversity Centre, Utrecht 3584 CT, The Netherlands; Institute of Biodiversity and Ecosystem Dynamics, University of Amsterdam, Amsterdam 1012 WX, The Netherlands.
Abstract:
The genus Scedosporium currently comprises six species, Scedosporium apiospermum, Scedosporium boydii, Pseudallescheria angusta, Scedosporium minutisporum, Scedosporium dehoogii, and Scedosporium aurantiacum, most of which can be distinguished with the primary fungal DNA barcode, the ITS1/2 region of the rDNA gene cluster. In the present study, four additional genetic loci were explored from a phylogenetic point of view enabling a barcoding approach based on K2P pairwise distances to resolve the taxa Scedosporium. We included partial γ-actin (ACT), β-tubulin (BT2), elongation factor 1α (TEF1), and the small ribosomal protein 60S L10 (L1) (RP60S). Phylogenetic inference of each marker individually showed that four out of six species within Scedosporium can be distinguished unambiguously, while strains of S. apiospermum, S. boydii, and P. angusta showed occasional recombination, and accordingly, no genealogical concordance between markers was obtainable. We defined S. apiospermum, S. boydii, and P. angusta as the 'S. apiospermum species complex' since observed differences were not consistent between lineages, and no clinical differences are known between entities within the complex. While BT2 revealed the best performance among the genetic loci tested at the lineage level, barcoding of the ITS region is sufficient for distinction of all entities in Scedosporium at the species or 'complex' level.
Insights
DNA barcoding effectively distinguishes Scedosporium species, with the ITS region sufficient for identifying all taxa. However, S. apiospermum, S. boydii, and P. angusta form a complex due to recombination, requiring additional markers like BT2 for lineage-level resolution.
Area of Science:
- Mycology
- Molecular Biology
- Fungal Taxonomy
Background:
- The genus Scedosporium includes medically important fungi.
- Accurate species identification is crucial for clinical management.
- Current DNA barcoding primarily uses the ITS1/2 region.
Purpose of the Study:
- To evaluate additional genetic loci for Scedosporium species resolution.
- To develop a robust DNA barcoding approach for Scedosporium.
- To clarify the taxonomic status of Scedosporium species.
Main Methods:
- Phylogenetic analysis of four additional genetic loci: ACT, BT2, TEF1, and RP60S.
- K2P pairwise distance-based barcoding approach.
- Comparison of marker performance for species discrimination.
Main Results:
- Four out of six Scedosporium species were unambiguously distinguished.
- S. apiospermum, S. boydii, and P. angusta exhibited recombination, forming the 'S. apiospermum species complex'.
- No genealogical concordance was found between markers for the complex, but BT2 showed best lineage-level performance.
Conclusions:
- The ITS region is sufficient for distinguishing Scedosporium at the species or complex level.
- The 'S. apiospermum species complex' requires further investigation.
- Additional genetic markers like BT2 aid in resolving deeper phylogenetic relationships within Scedosporium.
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