Development of a novel duplex recombinase polymerase amplification (DRPA) assay for rapid detection of carbapenem-resistant Acinetobacter baumannii

Carbapenem-Resistant Acinetobacter baumannii (CRAB) poses a major public health threat due to its multidrug resistance and high mortality rates, necessitating rapid and accurate diagnostic tools for timely intervention and infection control. This study developed and evaluated a novel detection method combining duplex recombinase polymerase amplification (DRPA) with a lateral flow strip (LFS) for the rapid visual identification of CRAB. The DRPA-LFS assay targets bla<sub>OXA-23</sub> and bla<sub>OXA-51</sub> genes, enabling isothermal amplification at 37 °C followed by a simple visual readout. The method demonstrated high sensitivity (10<sup>2</sup> CFU). Results can be obtained within 40 min without the need for complex instrumentation, making it suitable for resource-limited environments. the method offers a portable, user-friendly, and cost-effective solution for CRAB detection.

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Publication Details

Journal
BMC Infectious Diseases
Published
2026-03-24
DOI
https://doi.org/10.1186/s12879-026-13175-z
Primary Topic
Antibiotic Resistance in Bacteria
Type
article
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article

Development of a novel duplex recombinase polymerase amplification (DRPA) assay for rapid detection of carbapenem-resistant Acinetobacter baumannii

BMC Infectious Diseases
Antibiotic Resistance in Bacteria
article

Development of a novel duplex recombinase polymerase amplification (DRPA) assay for rapid detection of carbapenem-resistant Acinetobacter baumannii

article en

Abstract

Carbapenem-Resistant Acinetobacter baumannii (CRAB) poses a major public health threat due to its multidrug resistance and high mortality rates, necessitating rapid and accurate diagnostic tools for timely intervention and infection control. This study developed and evaluated a novel detection method combining duplex recombinase polymerase amplification (DRPA) with a lateral flow strip (LFS) for the rapid visual identification of CRAB. The DRPA-LFS assay targets bla<sub>OXA-23</sub> and bla<sub>OXA-51</sub> genes, enabling isothermal amplification at 37 °C followed by a simple visual readout. The method demonstrated high sensitivity (10<sup>2</sup> CFU). Results can be obtained within 40 min without the need for complex instrumentation, making it suitable for resource-limited environments. the method offers a portable, user-friendly, and cost-effective solution for CRAB detection.

BMC Infectious Diseases
Zhongda Hospital Southeast University (CN), The First People’s Hospital of Lianyungang (CN)
Good health and well-being
Openalex Percentile: Top 10%
Antibiotic Resistance in Bacteria
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