Does One Size Fit All? Variations in the DNA Barcode Gaps of Macrofungal Genera

Author:

Wilson Andrew W.1ORCID,Eberhardt Ursula2,Nguyen Nhu3,Noffsinger Chance R.4,Swenie Rachel A.4,Loucks Justin L.1,Perry Brian A.5ORCID,Herrera Mariana6,Osmundson Todd W.7ORCID,DeLong-Duhon Sarah8,Beker Henry J.910,Mueller Gregory M.6ORCID

Affiliation:

1. Denver Botanic Gardens, 909 York Street, Denver, CO 80206, USA

2. Staatliches Museum für Naturkunde Stuttgart, Rosenstein 1, 70191 Stuttgart, Germany

3. Department of Tropical Plant and Soil Sciences, University of Hawaiʻi at Mānoa, 3190 Maile Way, St. John 102, Honolulu, HI 96822, USA

4. Department of Ecology and Evolutionary Biology, University of Tennessee, Dabney Hall, 1416 Circle Drive, Knoxville, TN 37996, USA

5. Department of Biological Sciences, California State University East Bay, 25800 Carlos Bee Blvd., Hayward, CA 94542, USA

6. Chicago Botanic Garden, 1000 Lake Cook Road, Glencoe, IL 60022, USA

7. Biology Department, University of Wisconsin-La Crosse, 1725 State Street, La Crosse, WI 54601, USA

8. Department of Biology, The University of Iowa, Iowa City, IA 52245, USA

9. Royal Holloway College, University of London, London WC1E 7HU, UK

10. Plantentuin Meise, Nieuwelaan 38, B-1860 Meise, Belgium

Abstract

The nuclear ribosomal internal transcribed spacer (nrITS) region has been widely used in fungal diversity studies. Environmental metabarcoding has increased the importance of the fungal DNA barcode in documenting fungal diversity and distribution. The DNA barcode gap is seen as the difference between intra- and inter-specific pairwise distances in a DNA barcode. The current understanding of the barcode gap in macrofungi is limited, inhibiting the development of best practices in applying the nrITS region toward research on fungal diversity. This study examined the barcode gap using 5146 sequences representing 717 species of macrofungi from eleven genera, eight orders and two phyla in datasets assembled by taxonomic experts. Intra- and inter-specific pairwise distances were measured from sequence and phylogenetic data. The results demonstrate that barcode gaps are influenced by differences in intra- and inter-specific variance in pairwise distances. In terms of DNA barcode behavior, variance is greater in the ITS1 than ITS2, and variance is greater in both relative to the combined nrITS region. Due to the difference in variance, the barcode gaps in the ITS2 region are greater than in the ITS1. Additionally, the taxonomic approach of “splitting” taxa into numerous taxonomic units produces greater barcode gaps when compared to “lumping”. The results show variability in the barcode gaps between fungal taxa, demonstrating a need to understand the accuracy of DNA barcoding in quantifying species richness. For taxonomic studies, variability in nrITS sequence data supports the application of multiple molecular markers to corroborate the taxonomic and systematic delineation of species.

Funder

National Science Foundation

Publisher

MDPI AG

Subject

Plant Science,Ecology, Evolution, Behavior and Systematics,Microbiology (medical)

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