Rapid and accurate detection of carbapenem-resistance gene by isothermal amplification in Acinetobacter baumannii

Author:

Liu Shuang12,Huang Guangtao3,Gong Yali3,Jin Xiaojun4,Meng Yudan1,Peng Yizhi3,Zhao Junning5,Li Xiaolu65,Li Qin7

Affiliation:

1. Department of Plastic & Burns Surgery, The Affiliated Hospital of Southwest Medical University, Tai Ping Street, Luzhou, 646000, China

2. Department of Dermatology, Dazhou Central Hospital, Nanyue Temple Street, Dazhou, 635000, China

3. Institute of Burn Research, Southwest Hospital, The Army Medical University, Gao Tan Yan Street, Chongqing, 400038, China

4. Department of Emergency, The First Affiliated Hospital, Zhejiang University School of Medicine, Qingchun Road, Hangzhou, 310003, China

5. Sichuan Translational Medicine Center of Chinese Medicine, Sichuan Academy of Chinese Medical Sciences, Ren Min Nan Lu Road, Chengdu, 610041, China

6. School of Medicine, Chengdu University, Xindu Avenue, Chengdu 610106, China

7. Department of Infectious Diseases, The Affiliated Hospital of Southwest Medical University, Tai Ping Street, Luzhou, 646000, China

Abstract

Abstract Background Acinetobacter baumannii (A. baumannii) is one of the pivotal pathogens responsible for nosocomial infections, especially in patients with low immune response, and infection with carbapenem-resistant A. baumannii has been increasing in recent years. Rapid and accurate detection of carbapenem-resistance genes in A. baumannii could be of immense help to clinical staff. Methods In this study, a 15-μL reaction system for recombinase polymerase amplification (RPA) was developed and tested. We collected 30 clinical isolates of A. baumannii from the Burn Institute of Southwest Hospital of Third Military Medical University (Army Medical University) for 6 months and tested antibiotic susceptibility using the VITEK 2 system. A. baumannii was detected based on the blaOXA-51 gene by PCR, qPCR and 15 μL-RPA, respectively. Sensitivity and specificity were evaluated. In addition, PCR and 15 μL-RPA data for detecting the carbapenem-resistance gene blaOXA-23 were comparatively assessed. Results The detection limit of the blaOXA-51 gene by 15 μL RPA was 2.86 CFU/ml, with sensitivity comparable to PCR and qPCR. No positive amplification signals were detected in non-Acinetobacter isolates, indicating high specificity. However, only 18 minutes were needed for the 15 μL RPA assay. Furthermore, an antibiotic susceptibility test showed that up to 90% of A. baumannii strains were resistant to meropenem and imipenem; 15 μL RPA data for detecting blaOXA-23 showed that only 10% (n = 3) of A. baumannii isolates did not show positive amplification signals, and the other 90% of (n = 27) isolates were positive, corroborating PCR results. Conclusion We demonstrated that the new 15 μL RPA assay for detecting blaOXA-23 in A. baumannii is faster and simpler than qPCR and PCR. It is a promising alternative molecular diagnostic tool for rapid and effective detection of A. baumannii and drug-resistance genes in the field and point-of-care testing.

Funder

Science and Technology Research of Chinese Medical Sciences of Sichuan Province Pharmaceutical Administration

Key Field Technology Innovation of Southwest Hospital

National Natural Science Foundation of China

Publisher

Oxford University Press (OUP)

Subject

Critical Care and Intensive Care Medicine,Dermatology,Biomedical Engineering,Emergency Medicine,Immunology and Allergy,Surgery

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