AI Article Synopsis

  • * A study evaluated a new Sanger sequencing test on 25 pure culture samples, showing 100% sensitivity for clarithromycin and high sensitivity (93%) and specificity (92%) for levofloxacin resistance detection.
  • * In clinical tests on 112 patients, resistance mutations were found in 24% for clarithromycin and 23% for levofloxacin, with specific mutations identified, emphasizing the importance of personalized therapy to combat antibiotic resistance.

Article Abstract

The Maastricht VI/Florence consensus recommends, as one of the measures to enhance the efficacy of infection eradication, a personalized treatment approach involving the selection of an antimicrobial agent based on the pre-determined resistance of To address the need to develop test systems for personalized drug selection, this study was designed to analyze the molecular resistance of using a newly developed Sanger sequencing test platform. The characteristics of the test system were determined on 25 pure culture samples of with known resistance. Sensitivity and specificity for detecting resistance to clarithromycin was 100% and those to levofloxacin were 93% and 92%, respectively. The test system has been tested in real clinical practice on 112 -positive patients who had not previously received proton pump inhibitors (PPIs) or antibacterial drugs. Mutations indicating resistance to clarithromycin were found in 27 (24%) samples and those indicating resistance to levofloxacin were found in 26 (23%) samples. Double resistance was observed in 16 (14%) samples. The most common mutations leading to clarithromycin resistance were 2143G and 2142G and to levofloxacin resistance-261A and 271A in the gene, which account for 69% of all identified genetic determinants in levofloxacin-resistant bacteria. Thus, a personalized approach to the selection of eradication therapy based on the detection of bacterial resistance before prescribing first-line therapy could help to avoid the prescription of ineffective eradication therapies and, overall, contribute to the control of antibiotic resistance of .

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11276122PMC
http://dx.doi.org/10.3390/cimb46070397DOI Listing

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