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Microbiology spectrum2025; e0152925; doi: 10.1128/spectrum.01529-25

High-resolution melting curve FRET-qPCR rapidly distinguishes Streptococcus equi subsp. equi and zooepidemicus.

Abstract: We developed a fluorescence resonance energy transfer (FRET)-based real-time PCR (qPCR) assay coupled with high-resolution melting (HRM) analysis to differentiate subsp. (SEE) from subsp. (SEZ), two closely related equine pathogens with distinct clinical implications. The assay targets a region of the 23S rRNA gene containing single-nucleotide polymorphisms that differentiate the subspecies. By combining subspecies-specific probes with melting temperature () analysis, the assay accurately distinguished SEE, SEZ, and mixed infections without the need for post-PCR processing. The entire workflow-from DNA extraction to result interpretation-was completed in under 2 h. The assay demonstrated high sensitivity and specificity, detecting as few as one genome copy per reaction, and showed excellent reproducibility with 100% concordance to whole-genome sequencing (WGS) results. Notably, one nasal swab isolate biochemically identified as SEE (based on its fermentation profile) was reclassified as SEZ by the FRET-qPCR assay, a result confirmed by WGS. Among 127 equine clinical samples, SEE was detected in 18% (23/127) and SEZ in 82% (104/127). SEZ predominated in eye, sinus, transtracheal aspirate, uterine, and wound samples, whereas SEE was significantly associated with guttural pouch samples. This FRET-qPCR assay offers a rapid, accurate, and practical molecular diagnostic tool for distinguishing subspecies, supporting improved clinical management and outbreak control in equine populations. Objective: Accurately identifying the cause of respiratory infections in horses is essential for proper treatment and preventing outbreaks. This study introduces a rapid and reliable test that distinguishes between subsp. (which causes the serious disease strangles) and its close relative subsp. (which usually causes milder, less contagious infections). Traditional tests can be slow or give unclear results, especially for unusual strains. Our new one-step molecular test uses melting curve analysis to rapidly and accurately differentiate between these bacterial subspecies-even in mixed infections. The method, which matches the accuracy of whole-genome sequencing but is much faster and easier to use, can help veterinarians to make more accurate diagnoses and improve tracking and control of equine respiratory disease.
Publication Date: 2025-07-30 PubMed ID: 40736350DOI: 10.1128/spectrum.01529-25Google Scholar: Lookup
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  • Journal Article

Summary

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This research introduced a rapid and highly reliable test for distinguishing between two closely related equine pathogens, Streptococcus equi subsp. equi (SEE) and Streptococcus equi subsp. zooepidemicus (SEZ), using a fluorescence resonance energy transfer-based real-time PCR assay coupled with high-resolution melting analysis. The test can successfully identify the bacteria causing respiratory infections in horses with high sensitivity, specificity, and reproducibility, thus aiding in effective clinical management and outbreak control.

Methodology

  • The researchers developed a fluorescence resonance energy transfer (FRET)-based real-time PCR (qPCR) assay coupled with high-resolution melting (HRM) analysis. This assay targets a specific region of the 23S rRNA gene containing single-nucleotide polymorphisms that differentiate the sub-species.
  • By combining sub-species-specific probes with melting temperature (Tm) analysis, the assay could accurately distinguish SEE, SEZ, and mixed infections without needing post-PCR processing.
  • The study utilized an efficient workflow ranging from DNA extraction to result interpretation which was completed within two hours.

Findings and Implications

  • The assay demonstrated high sensitivity and specificity, detecting as low as one genome copy per reaction. It showed excellent reproducibility with 100% concordance to whole-genome sequencing (WGS) results.
  • Interestingly, one nasal swab isolate initially classified as SEE (based on its fermentation profile) was re-identified as SEZ by the FRET-qPCR assay. This reclassification was further confirmed by WGS.
  • Among the 127 equine clinical samples tested, SEE was found in 18% (23/127) and SEZ in 82% (104/127). SEZ was more common in eye, sinus, transtracheal aspirate, uterine, and wound samples, while SEE was significantly associated with guttural pouch samples.
  • The FRET-qPCR assay thus provides a quick, accurate, and practical diagnostic tool for distinguishing S. equi sub-species. This could support improved clinical management and outbreak control in equine populations. It could also assist veterinarians in making more exact diagnoses, thereby enhancing tracking and control of equine respiratory disease.

Cite This Article

APA
Iduu NV, Raiford D, Cohen ND, Landrock KK, Wang C. (2025). High-resolution melting curve FRET-qPCR rapidly distinguishes Streptococcus equi subsp. equi and zooepidemicus. Microbiol Spectr, e0152925. https://doi.org/10.1128/spectrum.01529-25

Publication

ISSN: 2165-0497
NlmUniqueID: 101634614
Country: United States
Language: English
Pages: e0152925

Researcher Affiliations

Iduu, Nneka Vivian
  • Molecular Diagnostic Laboratory, College of Veterinary Medicine, Auburn University, Auburn, Alabama, USA.
  • Department of Pathobiology, College of Veterinary Medicine, Auburn University, Auburn, Alabama, USA.
Raiford, Donna
  • Department of Pathobiology, College of Veterinary Medicine, Auburn University, Auburn, Alabama, USA.
  • Bacteriology and Mycology Laboratory, College of Veterinary Medicine, Auburn University, Auburn, Alabama, USA.
Cohen, Noah D
  • Department of Large Animal Clinical Sciences, College of Veterinary Medicine & Biomedical Sciences, Texas A&M University, College Station, Texas, USA.
Landrock, Kerstin K
  • Department of Large Animal Clinical Sciences, College of Veterinary Medicine & Biomedical Sciences, Texas A&M University, College Station, Texas, USA.
Wang, Chengming
  • Molecular Diagnostic Laboratory, College of Veterinary Medicine, Auburn University, Auburn, Alabama, USA.
  • Department of Pathobiology, College of Veterinary Medicine, Auburn University, Auburn, Alabama, USA.

Citations

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