4.6 Article

Novel real-time PCR based assays for differentiating fall armyworm strains using four single nucleotide polymorphisms

Journal

PEERJ
Volume 9, Issue -, Pages -

Publisher

PEERJ INC
DOI: 10.7717/peerj.12195

Keywords

Fall armyworm; Spodoptera frugiperda; Genetic strains; TaqMan; Diagnostic assay; Real-time PCR

Funding

  1. Agricultural and Food Research Initiative-Education and Workforce Development from the USDA National Institute of Food and Agriculture [2020-67034-31748]
  2. Agricultural and Food Research Initiative from the USDA National Institute of Food and Agriculture [2021-67013-33566]
  3. Agriculture and Food Research Initiative Foundational Program competitive grant [2018-67013-27820]
  4. Hatch Multistate from the US Department of Agriculture National Institute of Food and Agriculture [NC-246]
  5. USDA-APHIS [AP19PPQS, T00C071]

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The fall armyworm, Spodoptera frugiperda, is a polyphagous global pest that preferentially feeds on gramineous crops such as corn, sorghum, and pasture grasses. It consists of two genetically distinct host strains known as the corn and rice strains, complicating pest management approaches. Through molecular markers and TaqMan assays, researchers are able to differentiate between strains and interstrain hybrids, allowing for future studies on strain population dynamics and hybrids. Understanding the ecology of S. frugiperda strains is crucial for informing effective management strategies.
The fall armyworm, Spodoptera frugiperda, is a polyphagous global pest with a preference for gramineous crops such as corn, sorghum and pasture grasses. This species is comprised of two morphologically identical but genetically distinct host strains known as the corn and rice strains, which can complicate pest management approaches. Two molecular markers are commonly used to differentiate between strains, however, discordance between these markers can lead to inconclusive strain identification. Here, we used double digest restriction site associated DNA sequencing to identify diagnostic single nucleotide polymorphisms (SNPs) with alleles unique to each strain. We then used these strain-specific SNPs to develop four real-time PCR based TaqMan assays to rapidly and reliably differentiate between strains and interstrain hybrids. These assays provide a new tool for differentiating between strains in field-collected samples, facilitating future studies on strain population dynamics and interstrain hybridization rates. Understanding the basic ecology of S. frugiperda strains is necessary to inform future management strategies.

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