PhytoFrontiers (Mar 2024)

Development of a qPCR Assay for Species-Specific Detection of the Tar Spot Pathogen Phyllachora maydis

  • Emily M. Roggenkamp,
  • Jill C. Check,
  • Akshaya K. Biswal,
  • Crystal M. Floyd,
  • Laura A. Miles,
  • Camila P. Nicolli,
  • Sujoung Shim,
  • Catalina Salgado-Salazar,
  • Amos E. Alakonya,
  • Dean K. Malvick,
  • Damon L. Smith,
  • Darcy E. P. Telenko,
  • Martin I. Chilvers

DOI
https://doi.org/10.1094/PHYTOFR-04-23-0050-FI
Journal volume & issue
Vol. 4, no. 1
pp. 61 – 71

Abstract

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Phyllachora maydis is a fungal plant pathogen that causes tar spot of corn (Zea mays) in North and South America, causing devastating yield losses under favorable conditions. Although the causal agent is relatively easy to diagnose via macroscopic and microscopic observations, other diseases and conditions, such as insect frass, have been mistaken for tar spot of corn. Furthermore, conidia and ascospores in isolation can be difficult to visually distinguish from other fungi, and the development of signs and symptoms of the disease may not be observed until 12 to 20 days after infection. Therefore, we developed a TaqMan quantitative polymerase chain reaction (qPCR) assay for the detection and quantification of this pathogen to be used for diagnostics and airborne spore quantification. The assay was designed for the internal transcribed spacer region of P. maydis. The specificity of the assay was confirmed and tested against various nontarget Phyllachora species, corn pathogens, endophytes, and P. maydis samples from several states in the Midwest and from Mexico. The detection limit of this assay was determined to be 100 fg of genomic P. maydis DNA. To demonstrate the transferability of this technology, the assay was tested in different labs using various qPCR thermal cyclers. This assay can be used in downstream research involving latency period, disease prediction, and diagnostics. [Figure: see text] Copyright © 2024 The Author(s). This is an open access article distributed under the CC BY-NC-ND 4.0 International license.

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