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Target Recognition Initiated Self-Assembly-Based Signal Amplification Strategy for Sensitive and Colorimetric Staphylococcus aureus Detection and Diagnosis of Skin Infection. | LitMetric

AI Article Synopsis

  • Staphylococcus aureus (S. aureus) is a Gram-positive bacterium linked to various infections, particularly skin and soft tissue issues, but accurate detection is challenging.
  • Researchers developed a new colorimetric method that combines allosteric probe-based recognition and a chain extension process to enhance detection sensitivity and accuracy.
  • This method, which uses active DNAzyme and a color change system, can detect S. aureus in a range from 10 cfu/mL to 10^6 cfu/mL, with a limit of detection at 232 cfu/mL, making it a promising tool for biomedical research and clinical diagnostics.

Article Abstract

Staphylococcus aureus (S. aureus), as a Gram-positive bacterium, is commonly encountered in various infectious diseases, such as acute skin and soft tissue infections. Despite that many efforts have been made, sensitive and reliable quantitative determination of S. aureus remains a huge challenge. Here, we depict a novel colorimetric approach for sensitive and accurate detection by combining allosteric probe-based target recognition and chain extension-based dual signal recycling. The single-strand DNA (ssDNA) products generated by the chain extension process lead to the liberation of G-quadruplex sequences, which can fold into active DNAzyme under the assistance of hemin. The active DNAzyme can work as peroxidase mimics to catalyze the 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (ABTS)-HO system, causing the color change of the system. Eventually, the method exhibits a wide detection range from 10 cfu/mL to 10 cfu/mL. The limit of detection of the approach was determined 232 cfu/mL. Considering the robust capability of the approach in S. aureus detection, we believe that it will be a potential alternative tool for biomedical research and clinical molecular diagnostics.

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Source
http://dx.doi.org/10.1007/s12033-023-00791-2DOI Listing

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