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

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 carbape...

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Autores principales: Liu, Shuang, Huang, Guangtao, Gong, Yali, Jin, Xiaojun, Meng, Yudan, Peng, Yizhi, Zhao, Junning, Li, Xiaolu, Li, Qin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7462923/
https://www.ncbi.nlm.nih.gov/pubmed/32905076
http://dx.doi.org/10.1093/burnst/tkaa026
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author Liu, Shuang
Huang, Guangtao
Gong, Yali
Jin, Xiaojun
Meng, Yudan
Peng, Yizhi
Zhao, Junning
Li, Xiaolu
Li, Qin
author_facet Liu, Shuang
Huang, Guangtao
Gong, Yali
Jin, Xiaojun
Meng, Yudan
Peng, Yizhi
Zhao, Junning
Li, Xiaolu
Li, Qin
author_sort Liu, Shuang
collection PubMed
description 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 bla(OXA-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 bla(OXA-23) were comparatively assessed. RESULTS: The detection limit of the bla(OXA-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 bla(OXA-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 bla(OXA-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.
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spelling pubmed-74629232020-09-03 Rapid and accurate detection of carbapenem-resistance gene by isothermal amplification in Acinetobacter baumannii Liu, Shuang Huang, Guangtao Gong, Yali Jin, Xiaojun Meng, Yudan Peng, Yizhi Zhao, Junning Li, Xiaolu Li, Qin Burns Trauma Research Article 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 bla(OXA-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 bla(OXA-23) were comparatively assessed. RESULTS: The detection limit of the bla(OXA-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 bla(OXA-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 bla(OXA-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. Oxford University Press 2020-09-02 /pmc/articles/PMC7462923/ /pubmed/32905076 http://dx.doi.org/10.1093/burnst/tkaa026 Text en © The Author(s) 2020. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Liu, Shuang
Huang, Guangtao
Gong, Yali
Jin, Xiaojun
Meng, Yudan
Peng, Yizhi
Zhao, Junning
Li, Xiaolu
Li, Qin
Rapid and accurate detection of carbapenem-resistance gene by isothermal amplification in Acinetobacter baumannii
title Rapid and accurate detection of carbapenem-resistance gene by isothermal amplification in Acinetobacter baumannii
title_full Rapid and accurate detection of carbapenem-resistance gene by isothermal amplification in Acinetobacter baumannii
title_fullStr Rapid and accurate detection of carbapenem-resistance gene by isothermal amplification in Acinetobacter baumannii
title_full_unstemmed Rapid and accurate detection of carbapenem-resistance gene by isothermal amplification in Acinetobacter baumannii
title_short Rapid and accurate detection of carbapenem-resistance gene by isothermal amplification in Acinetobacter baumannii
title_sort rapid and accurate detection of carbapenem-resistance gene by isothermal amplification in acinetobacter baumannii
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7462923/
https://www.ncbi.nlm.nih.gov/pubmed/32905076
http://dx.doi.org/10.1093/burnst/tkaa026
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