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Bacterial gastroenteritis, characterized by diarrhea, abdominal cramps, and vomiting, is often caused by ingestion of contaminated food or water and is frequently associated with pathogenic Escherichia coli strains. These microbes exploit two principal mechanisms to inflict disease.Shiga toxin–producing E. coli, also referred to as STEC—notably O157:H7—release Shiga toxins that target ribosomes, blocking protein synthesis. The B subunit of the toxin binds the host glycolipid receptor...

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Introduce a novel, extremely sensitive aptamer against staphylococcal enterotoxin type D.

Arezoo Fallah1, Abbas Ali Imani Fooladi2, Hamid Sedighian2

  • 1Department of Bacteriology and Virology, Faculty of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.

International Journal of Biological Macromolecules
|February 2, 2025
PubMed
Summary

Researchers developed a novel DNA aptamer for detecting staphylococcal enterotoxin D (SED), a key cause of food poisoning. This aptamer offers a sensitive and specific tool for identifying this dangerous foodborne pathogen.

Keywords:
ELASASELEXSPRStaphylococcal enterotoxin DStaphylococcus aureusssDNA-aptamer

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Area of Science:

  • Biotechnology
  • Molecular Biology
  • Food Safety

Background:

  • Staphylococcus aureus is a major foodborne pathogen causing Staphylococcal food poisoning (SFP) through enterotoxins.
  • Rapid detection of staphylococcal enterotoxins (SEs) is crucial for public health.
  • Aptamers offer a promising alternative to antibodies for diagnostics due to their stability and cost-effectiveness.

Purpose of the Study:

  • To isolate high-affinity single-stranded DNA (ssDNA) aptamers specifically targeting staphylococcal enterotoxin D (SED).

Main Methods:

  • Systematic evolution of ligands by exponential enrichment (SELEX) was employed to identify aptamers.
  • Enzyme-linked apta-sorbent assay (ELASA) and surface plasmon resonance (SPR) were used for validation and affinity assessment.

Main Results:

  • SELEX yielded aptamers with significant binding affinity for SED.
  • Aptamer 1 demonstrated high specificity for SED with a dissociation constant (KD) of 4.4 ± 2.26 nM.
  • The limit of detection (LOD) for SED using this aptamer was 45 nM.

Conclusions:

  • The developed aptamer, when used in an ELASA system, provides enhanced specificity, sensitivity, and reproducibility for SED detection.
  • This novel aptamer holds potential for advanced diagnostic platforms targeting S. aureus enterotoxins.