Evidence map›Paper›PMID 26823635›Full record

ArticlePersoonia2015

One fungus, which genes? Development and assessment of universal primers for potential secondary fungal DNA barcodes.

J B Stielow, C A Lévesque, K A Seifert, W Meyer, L Iriny, D Smits, R Renfurm, G J M Verkley, M Groenewald, D Chaduli and 53 more

Abstract read
In one paragraph

Article in Persoonia, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 228 papers.

0numbers the graph read from it
0cells of the map it votes in
228citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

228 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Phylogeny ofPersoonia · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Basidiomycete Yeasts of Wine Grapes and Their Potential Applications in Winemaking.Comprehensive reviews in food science and food safety · 2025
    Review
  19. Article
  20. Article

168 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

63 authors.

J B StielowCBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.
C A LévesqueBiodiversity (Mycology and Microbiology), Agriculture and Agri-Food Canada, Ottawa, Ontario, Canada.
K A SeifertBiodiversity (Mycology and Microbiology), Agriculture and Agri-Food Canada, Ottawa, Ontario, Canada.
W MeyerMolecular Mycology Research Laboratory, Centre for Infectious Diseases and Microbiology, Marie Bashir Institute for Infectious Diseases and Biosecurity, Sydney, Australia; Medical School, Westmead Hospital, The University of Sydney, Westmead Millennium Institute, Westmead, Sydney, Australia.
L IrinyMolecular Mycology Research Laboratory, Centre for Infectious Diseases and Microbiology, Marie Bashir Institute for Infectious Diseases and Biosecurity, Sydney, Australia; Medical School, Westmead Hospital, The University of Sydney, Westmead Millennium Institute, Westmead, Sydney, Australia.
D SmitsCBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.
R RenfurmCBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.
G J M VerkleyCBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.
M GroenewaldCBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.
D ChaduliCIRM-INRA, UMR 1163 BBF, F-13288 Marseille, France.
A LomascoloCIRM-INRA, UMR 1163 BBF, F-13288 Marseille, France.; Aix-Marseille Université, Polytech, UMR 1163 BBF, F-13288 Marseille, France.
S WeltiUniversité Lille2, EA 4483, Laboratoire des Sciences Végétales et Fongiques, UFR Pharmacie, F-59006 Lille, France.
L Lesage-MeessenCIRM-INRA, UMR 1163 BBF, F-13288 Marseille, France.
A FavelCIRM-INRA, UMR 1163 BBF, F-13288 Marseille, France.; Aix-Marseille Université, Polytech, UMR 1163 BBF, F-13288 Marseille, France.
A M S Al-HatmiCBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.; Directorate General of Health Services, Ibri Hospital, Ministry of Health Oman, Sultanate of Oman.; Institute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, Amsterdam, The Netherlands.
U DammCBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.; Senckenberg Museum of Natural History, Görlitz, Germany.
N YilmazCBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.; Biodiversity (Mycology and Microbiology), Agriculture and Agri-Food Canada, Ottawa, Ontario, Canada.
J HoubrakenCBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.
L LombardCBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.
W QuaedvliegCBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.
M BinderCBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.
L A I VaasCBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.; Molecular Mycology Research Laboratory, Centre for Infectious Diseases and Microbiology, Marie Bashir Institute for Infectious Diseases and Biosecurity, Sydney, Australia; Medical School, Westmead Hospital, The University of Sydney, Westmead Millennium Institute, Westmead, Sydney, Australia.; Frauenhofer Institute for Molecular Biotechnology, Hamburg, Germany.
D VuCBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.
A YurkovDSMZ-Leibniz Institute German Collection of Microorganisms and Cell Cultures GmbH, Braunschweig, Germany.
D BegerowEvolution and Biodiversity of Plants, Geobotany, Ruhr-Universität Bochum, Bochum, Germany.
O RoehlEvolution and Biodiversity of Plants, Geobotany, Ruhr-Universität Bochum, Bochum, Germany.
M GuerreiroCentro de Recursos Microbiológicos, Departamento de Ciências da Vida, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, Portugal.
A FonsecaCentro de Recursos Microbiológicos, Departamento de Ciências da Vida, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, Portugal.
K SamerpitakCBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.; Department of Microbiology, Faculty of Medicine, Khon Kaen University, Thailand.; Institute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, Amsterdam, The Netherlands.
A D van DiepeningenCBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.
S DolatabadiCBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.; Institute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, Amsterdam, The Netherlands.
L F MorenoCBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.; Institute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, Amsterdam, The Netherlands.; Basic Pathology Department, Federal University of Paraná State, Curitiba, Paraná, Brazil.
S CasaregolaINRA UMR 1319, Micalis, CIRM-Levures, AgroParisTech, Thiverval-Grignon, France.
S MalletINRA UMR 1319, Micalis, CIRM-Levures, AgroParisTech, Thiverval-Grignon, France.
N JacquesINRA UMR 1319, Micalis, CIRM-Levures, AgroParisTech, Thiverval-Grignon, France.
L RosciniDepartment of Pharmaceutical Sciences, Microbiology, Università degli Studi di Perugia, Perugia, Italy.
E EgidiDipartimento di Scienze Ecologiche e Biologiche, Università degli Studi della Tuscia, Viterbo, Italy.; Department of Physiology Anatomy and Microbiology, School of Life Sciences, La Trobe University, 3083 Bundoora, Melbourne, Australia.
C BizetInstitut Pasteur, Unité de Mycologie Moléculaire, Centre National de Référence Mycoses Invasives et Antifongiques, Paris, France.; CNRS URA3012, Paris, France.
D Garcia-HermosoInstitut Pasteur, Unité de Mycologie Moléculaire, Centre National de Référence Mycoses Invasives et Antifongiques, Paris, France.; CNRS URA3012, Paris, France.
M P MartínDepartamento de Micología, Real Jardín Botánico, RJB-CSIC, Madrid, Spain.
S DengShanghai Institute of Medical Mycology, Changzheng Hospital, Second Military Medical University, Shanghai, China.
J Z GroenewaldCBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.
T BoekhoutCBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.; Shanghai Institute of Medical Mycology, Changzheng Hospital, Second Military Medical University, Shanghai, China.
Z W de BeerDepartment of Microbiology and Plant Pathology, Forestry Agricultural Biotechnology Institute (FABI), University of Pretoria, Pretoria, South Africa.
I BarnesDepartment of Genetics, Forestry Agricultural Biotechnology Institute (FABI), University of Pretoria, Pretoria, South Africa.
T A DuongDepartment of Genetics, Forestry Agricultural Biotechnology Institute (FABI), University of Pretoria, Pretoria, South Africa.
M J WingfieldDepartment of Microbiology and Plant Pathology, Forestry Agricultural Biotechnology Institute (FABI), University of Pretoria, Pretoria, South Africa.
G S de HoogCBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.; Institute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, Amsterdam, The Netherlands.; Biological Sciences Department, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia.
P W CrousCBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.; Department of Microbiology and Plant Pathology, Forestry Agricultural Biotechnology Institute (FABI), University of Pretoria, Pretoria, South Africa.; Microbiology, Department of Biology, Utrecht University, Utrecht, The Netherlands.
C T LewisBiodiversity (Mycology and Microbiology), Agriculture and Agri-Food Canada, Ottawa, Ontario, Canada.
S HambletonBiodiversity (Mycology and Microbiology), Agriculture and Agri-Food Canada, Ottawa, Ontario, Canada.
T A A MoussaBiological Sciences Department, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia.; Botany and Microbiology Department, Faculty of Science, Cairo University, Giza, Egypt.
H S Al-ZahraniBiological Sciences Department, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia.
O A AlmaghrabiBiological Sciences Department, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia.
G Louis-SeizeBiodiversity (Mycology and Microbiology), Agriculture and Agri-Food Canada, Ottawa, Ontario, Canada.
R AssabguiBiodiversity (Mycology and Microbiology), Agriculture and Agri-Food Canada, Ottawa, Ontario, Canada.
W McCormickBiodiversity (Mycology and Microbiology), Agriculture and Agri-Food Canada, Ottawa, Ontario, Canada.
G OmerCBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.
K DukikCBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.
G CardinaliDepartment of Pharmaceutical Sciences, Microbiology, Università degli Studi di Perugia, Perugia, Italy.
U EberhardtStaatliches Museum für Naturkunde Stuttgart, Abteilung Botanik, Stuttgart, Germany.; Ghent University, WE11 Biology, Gent, Belgium.
M de VriesCBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.
V RobertCBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to assess potential candidate gene regions and corresponding universal primer pairs as secondary DNA barcodes for the fungal kingdom, additional to ITS rDNA as primary barcode. Amplification efficiencies of 14 (partially) universal primer pairs targeting eight genetic markers were tested across > 1 500 species (1 931 strains or specimens) and the outcomes of almost twenty thousand (19 577) polymerase chain reactions were evaluated. We tested several well-known primer pairs that amplify: i) sections of the nuclear ribosomal RNA gene large subunit (D1-D2 domains of 26/28S); ii) the complete internal transcribed spacer region (ITS1/2); iii) partial β -tubulin II (TUB2); iv) γ-actin (ACT); v) translation elongation factor 1-α (TEF1α); and vi) the second largest subunit of RNA-polymerase II (partial RPB2, section 5-6). Their PCR efficiencies were compared with novel candidate primers corresponding to: i) the fungal-specific translation elongation factor 3 (TEF3); ii) a small ribosomal protein necessary for t-RNA docking; iii) the 60S L10 (L1) RP; iv) DNA topoisomerase I (TOPI); v) phosphoglycerate kinase (PGK); vi) hypothetical protein LNS2; and vii) alternative sections of TEF1α. Results showed that several gene sections are accessible to universal primers (or primers universal for phyla) yielding a single PCR-product. Barcode gap and multi-dimensional scaling analyses revealed that some of the tested candidate markers have universal properties providing adequate infra- and inter-specific variation that make them attractive barcodes for species identification. Among these gene sections, a novel high fidelity primer pair for TEF1α, already widely used as a phylogenetic marker in mycology, has potential as a supplementary DNA barcode with superior resolution to ITS. Both TOPI and PGK show promise for the Ascomycota, while TOPI and LNS2 are attractive for the Pucciniomycotina, for which universal primers for ribosomal subunits often fail.

Indexed as

DNA barcodingITS supplementmolecular taxonomyphylogenyspecies identificationuniversal primers

Identifiers

PMID26823635
PMCPMC4713107

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.