Utilizing Cell-SELEX, as a Promising Strategy to Isolate ssDNA Aptamer Probes for Detection of Staphylococcus aureus

  • Mitra Yazdi Yahyaabadi
  • Ghambar Sultan Dorraj
  • Mohammad Heiat
  • Ali Mohammad Latifi

Abstract

Staphylococcus aureus is one of the most important pathogens in hospital- acquired infections. Annually, many people are infected with S. aureus in hospitals. Rapid detection of this bacterium is extremely helpful in preventing and managing this bacterium mediated diseases. Aptamers are powerful probes, which can be used as a target explorer in a wide range of diagnostic systems.To isolate a specific aptamer against S. aureus, a library of single-stranded DNA molecules was designed, and enriched through Cell-SELEX procedure. In the Cell-SELEX, the DNA library was exposed to the S. aureus bacterium in 8 reiterative quadruple rounds including: binding, separation, elution and amplification. After 8 rounds, the PCR product was cloned and sequenced. Cloned aptameric sequences were evaluated through enzyme-linked oligonucleotide assay (ELONA), and a sequence with the best outcomes was selected as ideal aptamer. Eight rounds of Cell-SELEX procedure led to isolation of a specific ssDNA aptamer against S. aureus and
named as “STAPT” (conflation of STAphylococcus and APTamer). Using ELONA
3
technique, the detection limit of this aptamer was determined as 4 × 10 CFU/ml. The aptamer “STAPT” showed the promising and potent abilities and features to be utilized as a bio-detection element likely in advanced detection systems. Although
more extended researches are needed for this purpose.

Published
2018-03-13
How to Cite
YAZDI YAHYAABADI, Mitra et al. Utilizing Cell-SELEX, as a Promising Strategy to Isolate ssDNA Aptamer Probes for Detection of Staphylococcus aureus. Journal of Applied Biotechnology Reports, [S.l.], v. 4, n. 3, p. 633-638, mar. 2018. ISSN 2423-5784. Available at: <https://journals.bmsu.ac.ir/jabr/index.php/jabr/article/view/209>. Date accessed: 22 june 2018.
Section
Original/Research Articles

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