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The Application of Open Searching-based Approaches for the Identification of Acinetobacter baumannii O-linked Glycopeptides
Published on: November 2, 2021
Carbapenem-resistant Acinetobacter baumannii carrier detection: a simple and efficient protocol
Jonathan Lellouche1,2, Alona Keren-Paz1, Reut Rov1
1National Institute for Antibiotic Resistance and Infection Control, Ministry of Health, Tel Aviv, Israel.
A new protocol using skin sampling and modified CHROMagar Acinetobacter (mCaA) effectively detects carbapenem-resistant Acinetobacter baumannii (CRAB) carriers. This method offers a rapid and reliable 24-hour turnaround for infection control.
Area of Science:
- Clinical Microbiology
- Infectious Diseases
- Molecular Diagnostics
Background:
- Carbapenem-resistant Acinetobacter baumannii (CRAB) is a critical multidrug-resistant pathogen causing significant nosocomial infections.
- Standardized laboratory methods for CRAB carrier identification are lacking, hindering effective infection control strategies.
- WHO and CDC highlight CRAB as a major public health threat requiring urgent detection and management.
Purpose of the Study:
- To develop and validate a practical, sensitive, and specific protocol for detecting CRAB carriers from screening samples.
- To compare the performance of different selective agar media for CRAB isolation.
- To optimize sample enrichment time and identify the most accurate PCR-based methods for CRAB identification.
Main Methods:
- Evaluated three selective agar media: mSuperCARBA (SC), CHROMagar Acinetobacter (CaA), and modified CHROMagar Acinetobacter (mCaA) with meropenem.
- Assessed PCR for species-specific genes (gyrB, blaOXA-51) and carbapenemase genes (blaOXA-23, blaOXA-24, blaOXA-58).
- Conducted a prospective study using skin sampling with a 6-hour enrichment period, followed by plating on mCaA and PCR confirmation.
Main Results:
- Modified CHROMagar Acinetobacter (mCaA) demonstrated high specificity (97%) and sensitivity (98%) for CRAB detection.
- Skin sampling with a 6-hour enrichment achieved 98% sensitivity for CRAB carriage detection.
- PCR targeting gyrB (98% accuracy) and blaOXA-51 (99% accuracy) effectively differentiated CRAB from other species on mCaA.
Conclusions:
- A novel protocol combining skin sampling, short enrichment, mCaA selection, and PCR-based identification provides reliable and rapid CRAB carrier detection.
- This protocol achieves a 24-hour turnaround time, facilitating timely implementation of infection control measures.
- The developed method addresses the need for standardized and efficient CRAB screening in healthcare settings.
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