Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 11 de 11
Filter
Add more filters










Publication year range
1.
J Fungi (Basel) ; 9(8)2023 Jul 26.
Article in English | MEDLINE | ID: mdl-37623559

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.

2.
Pathogens ; 11(2)2022 Feb 15.
Article in English | MEDLINE | ID: mdl-35215194

ABSTRACT

Epidemiological models are important for the understanding of disease progression in plants and for the design of control strategies. Phytophthora ramorum, the pathogen responsible for the disease known as Sudden Oak Death, causes lethal infection on several oaks but relies on California bay laurels for transmission. Here, repeated surveys of bay laurels and oaks indicated that bay laurel disease incidence was positively correlated with rainfall, bay laurel density, and an eastern aspect, and negatively correlated with bay laurel basal area. Oak infection only occurred in years when rainfall was higher than the 30-year average, and although infection rates were greater among larger trees, mortality was greater among smaller trees. Additionally, larger oaks closer to infected bay laurels exhibited greater infection rates. Disease incidence differed among sites, and only a fraction of bay laurels were disease superspreaders, while even fewer individuals were refugial trees harboring active infections during dry periods. Based on this study, reducing bay laurel density in denser stands and the number of superspreaders or refugial trees in less dense stands may reduce disease incidence. However, the selective removal of bay laurel trees 0-10 m from oaks is likely to be more effective in preventing infection of specific oaks.

3.
Mycologia ; 108(2): 414-40, 2016.
Article in English | MEDLINE | ID: mdl-26740539

ABSTRACT

Lactarius (Russulales) is an important component of ectomycorrhizal fungal communities in cold-dominated contiguous arctic and disjunct alpine habitats where it associates primarily with Betula, Dryas and Salix However, little is known of this genus in the central and southern Rocky Mountain alpine zone (3000-3900 m) of North America. Molecular phylogenetic analyses of nuc rDNA ITS1-5.8S-ITS2 (ITS barcode) and the second largest subunit of the RNA polymerase II gene (RPB2) partial sequences in conjunction with detailed morphological examination confirm at least six species occurring above treeline. Most have intercontinental distributions in North America and Eurasia according to molecular comparison with type material and collections from Europe, Fennoscandia, Svalbard and Alaska. Rocky Mountain collections of L. lanceolatus (subgenus Russularia), along with the type from Alaska are paraphyletic with respect to L. aurantiacus and North American taxa L. luculentus and L. luculentus v. laetus Rocky Mountain collections of L. nanus, L. glyciosmus, L. repraesentaneus and L. salicis-reticulatae (subgenus Piperites) all form clades with European material from type localities and other arctic-alpine habitats. The arctic-alpine L. pseudouvidus/L. brunneoviolaceus group appears to be a complex containing additional taxa. North American material originally described as part of this group is well-separated phylogenetically and is described here as L. pallidomarginatus sp. nov. Lactarius lanceolatus, L. nanus and L. salicis-reticulatae appear largely restricted to arctic-alpine habitats with Salix Lactarius glyciosmus and L. repraesentaneus occur in arctic-alpine, subalpine and boreal habitats with Betula and also Picea and possibly Salix for the latter. Species distributions are hypothesized to be shaped by host ranges, glaciation and long distance dispersal.


Subject(s)
Basidiomycota/classification , Basidiomycota/genetics , Mycorrhizae/classification , Mycorrhizae/genetics , Altitude , Basidiomycota/physiology , Fruiting Bodies, Fungal/classification , Phylogeny , Species Specificity , United States
4.
PLoS One ; 8(4): e62419, 2013.
Article in English | MEDLINE | ID: mdl-23638077

ABSTRACT

Despite recent advances spearheaded by molecular approaches and novel technologies, species description and DNA sequence information are significantly lagging for fungi compared to many other groups of organisms. Large scale sequencing of vouchered herbarium material can aid in closing this gap. Here, we describe an effort to obtain broad ITS sequence coverage of the approximately 6000 macrofungal-species-rich herbarium of the Museum of Natural History in Venice, Italy. Our goals were to investigate issues related to large sequencing projects, develop heuristic methods for assessing the overall performance of such a project, and evaluate the prospects of such efforts to reduce the current gap in fungal biodiversity knowledge. The effort generated 1107 sequences submitted to GenBank, including 416 previously unrepresented taxa and 398 sequences exhibiting a best BLAST match to an unidentified environmental sequence. Specimen age and taxon affected sequencing success, and subsequent work on failed specimens showed that an ITS1 mini-barcode greatly increased sequencing success without greatly reducing the discriminating power of the barcode. Similarity comparisons and nonmetric multidimensional scaling ordinations based on pairwise distance matrices proved to be useful heuristic tools for validating the overall accuracy of specimen identifications, flagging potential misidentifications, and identifying taxa in need of additional species-level revision. Comparison of within- and among-species nucleotide variation showed a strong increase in species discriminating power at 1-2% dissimilarity, and identified potential barcoding issues (same sequence for different species and vice-versa). All sequences are linked to a vouchered specimen, and results from this study have already prompted revisions of species-sequence assignments in several taxa.


Subject(s)
DNA Barcoding, Taxonomic/methods , DNA, Fungal/genetics , Fungi/genetics , Biodiversity , DNA, Fungal/isolation & purification , Databases, Nucleic Acid , Museums , Polymerase Chain Reaction , Sequence Analysis, DNA
5.
Mycologia ; 105(4): 888-95, 2013.
Article in English | MEDLINE | ID: mdl-23709482

ABSTRACT

Solioccasus polychromus gen. & sp. nov., the most brightly colored hypogeous fungus known, is described from Papua New Guinea and tropical northern Australia south into subtropical forests along the Queensland coast and coastal mountains to near Brisbane. Phylogenetic analysis of molecular data places it as a sister genus to Bothia in the Boletineae, a clade of predominantly ectomycorrhizal boletes. Ectomycorrhizal trees, such as members of the Myrtaceae (Eucalyptus, Corymbia, Lophostemon, Melaleuca spp.) and Allocasuarina littoralis, were present usually in mixture or in some cases dominant, so we infer some or all of them to be among the ectomycorrhizal hosts of S. polychromus.


Subject(s)
Basidiomycota/classification , Mycorrhizae/classification , Australasia , Myrtaceae/microbiology , Papua New Guinea , Phylogeny
6.
Mol Ecol Resour ; 13(1): 66-74, 2013 Jan.
Article in English | MEDLINE | ID: mdl-23121735

ABSTRACT

The ubiquity, high diversity and often-cryptic manifestations of fungi and oomycetes frequently necessitate molecular tools for detecting and identifying them in the environment. In applications including DNA barcoding, pathogen detection from plant samples, and genotyping for population genetics and epidemiology, rapid and dependable DNA extraction methods scalable from one to hundreds of samples are desirable. We evaluated several rapid extraction methods (NaOH, Rapid one-step extraction (ROSE), Chelex 100, proteinase K) for their ability to obtain DNA of quantity and quality suitable for the following applications: PCR amplification of the multicopy barcoding locus ITS1/5.8S/ITS2 from various fungal cultures and sporocarps; single-copy microsatellite amplification from cultures of the phytopathogenic oomycete Phytophthora ramorum; probe-based P. ramorum detection from leaves. Several methods were effective for most of the applications, with NaOH extraction favored in terms of success rate, cost, speed and simplicity. Frozen dilutions of ROSE and NaOH extracts maintained PCR viability for over 32 months. DNA from rapid extractions performed poorly compared to CTAB/phenol-chloroform extracts for TaqMan diagnostics from tanoak leaves, suggesting that incomplete removal of PCR inhibitors is an issue for sensitive diagnostic procedures, especially from plants with recalcitrant leaf chemistry. NaOH extracts exhibited lower yield and size than CTAB/phenol-chloroform extracts; however, NaOH extraction facilitated obtaining clean sequence data from sporocarps contaminated by other fungi, perhaps due to dilution resulting from low DNA yield. We conclude that conventional extractions are often unnecessary for routine DNA sequencing or genotyping of fungi and oomycetes, and recommend simpler strategies where source materials and intended applications warrant such use.


Subject(s)
DNA Barcoding, Taxonomic/methods , DNA/isolation & purification , Fagaceae/microbiology , Fungi/genetics , Nucleic Acid Amplification Techniques/methods , Phytophthora/genetics , Sodium Hydroxide/chemistry , Cetrimonium , Cetrimonium Compounds , Chloroform , Endopeptidase K/chemistry , Genotype , Phenol , Plant Leaves/chemistry , Plant Leaves/microbiology , Polynesia , Resins, Synthetic/chemistry , Specimen Handling/methods
7.
Mycologia ; 104(4): 951-61, 2012.
Article in English | MEDLINE | ID: mdl-22495445

ABSTRACT

Sutorius is described as a new genus of Boletaceae to accommodate Boletus robustus originally named illegitimately by C.C. Frost from eastern North America. The legitimate name, Boletus eximius, provided by C.H. Peck, has been used since for a dark purple to chocolate brown bolete with finely scaly stipe and reddish brown spore deposit. This iconic taxon has been documented on five continents. Despite the straightforward species identification from morphology, the interpretation of stipe macro-morphology and spore color has led to equivocal generic placement. Phylogenetic analyses of genes encoding large subunit rRNA and translation elongation factor 1α confirm Sutorius as a unique generic lineage in the Boletaceae. Two species are recognized based on multiple accessions: S. eximius, represented by collections from North America, Costa Rica, Guyana, Indonesia and Japan (molecular data are lacking for only the Guyanan and Japanese material); and S. australiensis, represented by material from Queensland, Australia. Additional collections from Zambia and Thailand represent independent lineages, but sampling is insufficient to describe new species for these entities.


Subject(s)
Basidiomycota/classification , DNA, Fungal/genetics , Basidiomycota/cytology , Basidiomycota/genetics , Basidiomycota/metabolism , Color , Ecosystem , Genes, rRNA , Mycological Typing Techniques , Peptide Elongation Factor 1/genetics , Phylogeny , Phylogeography , Pigments, Biological/metabolism , Ribosome Subunits, Large, Eukaryotic/genetics , Sequence Alignment , Sequence Analysis, DNA , Species Specificity , Trees/microbiology
8.
Mitochondrial DNA ; 22 Suppl 1: 52-70, 2011 Oct.
Article in English | MEDLINE | ID: mdl-21299446

ABSTRACT

BACKGROUND AND AIMS: Here we describe preliminary efforts to integrate DNA barcoding into an ongoing inventory of the Lower Congo River (LCR) ichthyofauna. The 350 km stretch of the LCR from Pool Malebo to Boma includes the world's largest river rapids. The LCR ichthyofauna is hyperdiverse and rich in endemism due to high habitat heterogeneity, numerous dispersal barriers, and its downstream location in the basin. MATERIALS AND METHODS: We have documented 328 species from the LCR, 25% of which are thought to be endemic. In addition to detailing progress made to generate a reference sequence library of DNA barcodes for these fishes, we ask how DNA can be used at the current stage of the Fish Barcode of Life initiative, as a work in progress currently of limited utility to a wide audience. Two possibilities that we explore are the potential for DNA barcodes to generate discrete diagnostic characters for species, and to help resolve problematic taxa lacking clear morphologically diagnostic characters such as many species of the cyprinid genus Labeo, which we use as a case study. RESULTS: Our molecular analysis helped to clarify the validity of some species that were the subject of historical debate, and we were able to construct a molecular key for all monophyletic and morphologically recognizable species. Several species sampled from across the Congo Basin and widely distributed throughout Central and West Africa were recovered as paraphyletic based on our molecular data. CONCLUSION: Our study underscores the importance of generating reference barcodes for specimens collected from, or in close proximity to, type localities, particularly where species are poorly understood taxonomically and the extent of their geographical distributions have yet to be established.


Subject(s)
Cyprinidae/classification , DNA Barcoding, Taxonomic/methods , DNA, Mitochondrial/genetics , Electron Transport Complex IV/genetics , Fishes/classification , Rivers , Animals , Base Sequence , Congo , Cyprinidae/genetics , Democratic Republic of the Congo , Evolution, Molecular , Fish Proteins/genetics , Fishes/genetics , Homeodomain Proteins/genetics , Molecular Sequence Data , Phylogeny , Sequence Analysis, DNA , Species Specificity
9.
Mycol Res ; 112(Pt 4): 437-47, 2008 Apr.
Article in English | MEDLINE | ID: mdl-18316181

ABSTRACT

The obligate association of boletes with their plant partners is critical to understanding biogeographic distribution of these fungi. Only in rare instances are boletes not obligatory associates of plants; the majority are presumed or proven partners in obligate symbioses with a variety of plants. The array of plant-associated distributions provides a potential handle for evaluating bolete distribution on a global scale. However, migration processes remain unclear and distributions are often disjunct. As an illustration of phylogeographic studies of putatively widespread bolete taxa, we present preliminary analyses for Tylopilus ballouii using LSU rDNA and RPB1 sequence data. The LSU data suggest geographic structuring of the tested accessions. However, RPB1 data indicate that long-distance dispersal events (possibly mediated by humans) are possible, or that selection or other factors have obscured geographical patterns. Molecular divergence between samples in RPB1 argues against panmixis, and indicates that populations have been isolated for long periods.


Subject(s)
Basidiomycota/classification , Demography , Basidiomycota/growth & development , Basidiomycota/isolation & purification , Basidiomycota/physiology , Evolution, Molecular , Genetic Speciation , Geography , Phylogeny
10.
Mycorrhiza ; 17(3): 217-222, 2007 May.
Article in English | MEDLINE | ID: mdl-17216498

ABSTRACT

This study examines evidence for a particular arbutoid mycorrhizal interaction in páramo, a high-altitude neotropical ecosystem important in hydrological regulation but poorly known in terms of its fungal communities. Comarostaphylis arbutoides Lindley (Ericaceae) often forms dense thickets in Central American páramo habitats. Based on phylogenetic classification, it has been suggested that C. arbutoides forms arbutoid mycorrhizae with diverse Basidiomycetes and Ascomycetes; however, this assumption has not previously been confirmed. Based on field data, we hypothesized an arbutoid mycorrhizal association between C. arbutoides and the recently described bolete Leccinum monticola Halling & G.M. Mueller; in this study, we applied a rigorous approach using anatomical and molecular data to examine evidence for such an association. We examined root samples collected beneath L. monticola basidiomes for mycorrhizal structures, and we also compared rDNA internal transcribed spacer (ITS) sequences between mycorrhizal root tips and leaf or basidiome material of the suspected symbionts. Root cross sections showed a thin hyphal sheath and intracellular hyphal coils typical of arbutoid mycorrhizae. DNA sequence comparisons confirmed the identity of C. arbutoides and L. monticola as the mycorrhizal symbionts. In addition, this paper provides additional evidence for the widespread presence of minisatellite-like inserts in the ITS1 spacer in Leccinum species (including a characterization of the insert in L. monticola) and reports the use of an angiosperm-specific ITS primer pair useful for amplifying plant DNA from mycorrhizal roots without co-amplifying fungal DNA.


Subject(s)
Mycorrhizae/genetics , Base Sequence , Basidiomycota/genetics , Basidiomycota/isolation & purification , Basidiomycota/physiology , Costa Rica , DNA Primers/genetics , DNA, Fungal/genetics , DNA, Fungal/isolation & purification , DNA, Plant/genetics , DNA, Plant/isolation & purification , Ecosystem , Ericaceae/genetics , Ericaceae/microbiology , Ericaceae/physiology , Molecular Sequence Data , Mycorrhizae/physiology , Symbiosis
11.
Mycologia ; 97(5): 949-72, 2005.
Article in English | MEDLINE | ID: mdl-16596948

ABSTRACT

The alpine zone is comprised of habitats at elevations above treeline, and macromycetes play important ecological roles as decomposers and mycorrhizal symbionts here as elsewhere. Laccaria is an important group of ectomycorrhizal basidiomycetes widely used in experimental and applied research. A systematic study of alpine Laccaria species using morphological, cultural and molecular (ribosomal DNA internal transcribed spacer) data revealed five taxa in the Rocky Mountain alpine zone: L. laccata var. pallidifolia, L. nobilis (the first published report for arctic-alpine habitats), L. pumila, L. montana and L. pseudomontana (a newly described taxon similar to L. montana with more ellipsoidal, finely echinulate basidiospores). All occur in the southern Rocky Mountains of Colorado; however, only L. pumila and L. montana were found on the Beartooth Plateau in the northern Rocky Mountains of Montana and Wyoming. All are associated with dwarf and shrub Salix species, with L. laccata var. pallidifolia also associated with Dryas octopetala and Betula glandulosa. Maximum-parsimony phylogenetic analysis of rDNA-ITS sequences for 27 Laccaria accessions supports the morphological species delineations.


Subject(s)
Agaricales/classification , Agaricales/cytology , Ecosystem , Plants/microbiology , Agaricales/genetics , Agaricales/isolation & purification , Agaricales/physiology , Altitude , Betula/microbiology , Colorado , DNA, Fungal/chemistry , DNA, Fungal/genetics , DNA, Ribosomal Spacer/chemistry , DNA, Ribosomal Spacer/genetics , Environment , Molecular Sequence Data , Montana , Phylogeny , Rosaceae/microbiology , Salix/microbiology , Sequence Analysis, DNA , Wyoming
SELECTION OF CITATIONS
SEARCH DETAIL
...