Emerging Molecular Biomarkers for Early Detection of Antimicrobial Resistance in Clinical Pathogens
A Diagnostic Laboratory-Based Study
Bibliographic Data
| ID | 13133173 |
|---|---|
| Authors | Fahad Sami Abuong (Prince Mohammed bin Abdulaziz Hospital, corresponding author), Majed Hashem Fallatah (Prince Mohammed bin Abdulaziz Hospital), Mohammed Aljuhani (Prince Mohammed bin Abdulaziz Hospital), Hanan ahmed Alhirbish (Prince Mohammed bin Abdulaziz Hospital), Wejdan mohammed Terkustani (Prince Mohammed bin Abdulaziz Hospital), Nouf Oqla Alahmadi (Prince Mohammed bin Abdulaziz Hospital), Razan Faleh Alsubhi (King Abdulaziz Hospital), Sara Ali Shamlan (King Abdulaziz Hospital), Amal Mohammed Aqeeli (King Abdulaziz Hospital), S RASHEED (King Abdulaziz Hospital), Mashael Mohammed alneami (King Abdulaziz Hospital), Shams Nahi Albeladi (King Abdulaziz Hospital) |
| Year | 2025 |
| Volume | 3 |
| Issue | 3 |
| Pages | 395-429 |
| Publication date | 2025-11-20 |
| Open Access | Yes |
| Type | ARTICLE |
| Venue | Journal of Posthumanism (JOURNAL) |
| Journal identifiers | ISSN: 2634-3576 • E-ISSN: 2634-3584 |
| Publisher | Nobel Press Resources (PUBLISHER) |
| DOI | 10.63332/joph.v3i3.3678 |
| OpenAlex | W4416416953 |
| Language | EN |
Background: The global rise of antimicrobial resistance is a serious threat to public health. Conventional culture-based AST is time-consuming, taking 48-72 hours, thus delaying the start of appropriate therapy. The performance of a multiplex molecular panel targeting emerging AMR biomarkers for the rapid detection of resistance in Gram-negative and Gram-positive bacterial pathogens was evaluated directly from clinical specimens and positive blood cultures. Methods: Over a period of 12 months, we typed 1,250 clinical specimens (750 blood cultures and 500 respiratory samples) for the presence of resistance genes by an in-house multiplex PCR coupled to a microarray-based detection system. The panel targeted major resistance markers: blaKPC, blaNDM, blaOXA-48-like (carbapenemases), *mcr-1* (colistin resistance), mecA (methicillin resistance), and vanA/vanB (vancomycin resistance). Results were compared with standard phenotypic AST (VITEK 2 and broth microdilution) as the reference standard. Results: The molecular assay had an overall sensitivity of 98.2% and a specificity of 99.5% compared to phenotypic AST. The median TAT for reporting by molecular assay post-receipt of specimen was 4.5 hours as compared to 48 hours for conventional AST. It correctly identified 45 carbapenemase producers, 120 MRSA isolates, and 15 VRE isolates that were further confirmed phenotypically. It also detected the *mcr-1* gene in two E. coli isolates from blood cultures that showed high colistin MICs on confirmation. Conclusion: Molecular detection of AMR biomarkers allows for the early identification of resistant pathogens with a high degree of speed and accuracy. Implementation of these assays within diagnostic laboratories is critical to markedly reduce the time to effective therapy, to assist infection control practices, and ultimately to improve patient outcomes in the setting of the increasing crisis due to AMR
Antibiotic resistance · Antimicrobial · Colistin · Drug resistance · Molecular diagnostics · Multiplex · Multiplex polymerase chain reaction · Antibiotic Resistance in Bacteria · Bacterial Identification and Susceptibility Testing · Biosensors and Analytical Detection
| Highly cited | No |
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