Comparative analysis uncovers the limitations of current molecular detection methods for Fusarium oxysporum f. sp. cubense race 4 strains

PLoS One. 2019 Sep 23;14(9):e0222727. doi: 10.1371/journal.pone.0222727. eCollection 2019.

Abstract

Fusarium oxysporum f. sp. cubense Tropical Race 4 (Foc TR4) is threatening banana production worldwide. Despite quarantine efforts, the pathogen continues to spread; thus, early diagnosis plays an essential role for the proper execution of contingency plans. Here, we assess the accuracy of four PCR-based molecular methods described in the literature for the identification and detection of race 4 strains, including Subtropical (Foc STR4) and Tropical Race 4 causing Fusarium wilt of banana. We screened a total of 302 isolates using these four markers, and performed phylogenetic analyses, Vegetative Compatibility Group (VCG) testing, sequence comparison, and pathogenicity tests for selected isolates. Our results show that three out of the four markers tested are not reliable for identification of Foc STR4 and TR4, as DNA from isolates from Ecuador, pathogenic and nonpathogenic to banana, obtained from different banana cultivars, displayed cross-reaction with these methods; that is, false positives can occur during the diagnostic process for race 4. Phylogenetic analyses, VCG testing, sequence comparison, and pathogenicity tests suggest the presence of non-target F. oxysporum isolates that share genomic regions with pathogenic strains but lack true pathogenicity to banana. The findings of this work are of foremost importance for international regulatory agencies performing surveillance tests in pathogen-free areas using the current diagnostic methods. We suggest the use of a genetic locus possibly related to virulence, previously identified by T-DNA, and amplified with primers W2987F/ W2987R, for diagnosis of Foc TR4 as the most reliable alternative. We urge the adoption of a more holistic view in the study of F. oxysporum as a plant pathogen that considers the biology and diversity of the species for the development of better diagnostic tools.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • DNA Primers / genetics*
  • DNA, Fungal / analysis
  • DNA, Fungal / genetics*
  • Fusarium / classification
  • Fusarium / genetics*
  • Fusarium / pathogenicity
  • Musa / microbiology
  • Phylogeny
  • Plant Diseases / microbiology
  • Random Amplified Polymorphic DNA Technique / methods*
  • Sequence Analysis, DNA / methods*
  • Species Specificity
  • Virulence / genetics

Substances

  • DNA Primers
  • DNA, Fungal

Grants and funding

This project was supported by the National Secretariat of Higher Education of Ecuador (SENESCYT) by way of the scholarship program “Universidades de Excelencia”, the Graduate International Research Competitive Grant from the International Agriculture and Development (INTAD) program, the James F. and Marilyn L. Tammen Endowment of the Plant Pathology and Environmental Microbiology Department from The Pennsylvania State University, and by the USDA National Institute of Food and Agriculture Federal Appropriations under Project PEN04676 and Accession number 1017795 to MdMJG. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.