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比色环介导等温扩增法快速检测五大碳青霉烯酶家族(bla KPC、bla NDM、bla VIM、bla IMP 和 bla OXA-48-Like)的系统设计
Authors Feng W, Niu S, Chang Y, Jia X, Huang S, Yang P
Received 13 January 2021
Accepted for publication 7 May 2021
Published 24 May 2021 Volume 2021:14 Pages 1865—1874
DOI https://doi.org/10.2147/IDR.S301757
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 4
Editor who approved publication: Dr Héctor M. Mora-Montes
Purpose: Carbapenemase-producing Enterobacteriaceae (CPE) infection constitutes a public health threat. Timely and efficient diagnosis is of paramount importance for prompt and effective therapy. In order to quickly and comprehensively detect the five major families of carbapenemases (bla KPC, bla NDM, bla VIM, bla IMP, and bla OXA-48-like), colorimetric loop-mediated isothermal amplification (LAMP) was employed.
Materials and Methods: Five sets of LAMP primers were designed, each of which can, respectively, amplify all the carbapenemase subtypes described in this work. Twenty whole genome sequencing-verified-“standard strains”, including 1 bla NDM-1, 1 bla NDM-5, 1 bla NDM-6, 1 bla NDM-7, 2 bla IMP-4, 1 bla IMP-8, 2 bla KPC-2, 1 bla KPC-3, 1 bla KPC-4, 1 bla KPC-5, 1 bla KPC-6, 1 bla KPC-7, 1 bla OXA-48 and 1 bla OXA-181 carrier, and 1 bla VIM and bla OXA-244, 1 bla KPC-2 and bla IMP-4, 1 bla KPC-2 and bla VIM-1 and 1 bla KPC-2 and bla NDM-1-co-carriers, were used to establish a 25-microliter visual LAMP reaction system (kept at 65°C for 30 minutes in water bath). Color change from bright pink to yellow indicated positive amplification. In addition, 126 pre-verified clinical carbapenem-resistant Enterobacteriaceae (CRE) isolates, including 65 CPE (23 bla NDM, 2 bla OXA-48-like, 1 bla KPC and bla VIM, 2 bla IMP, and 37 bla KPC carriers) and 61 non-CPE, were also detected.
Results: With the lowest detection limit of 10 colony forming units (CFU) per reaction for LAMP and 103 CFU per reaction for PCR, the LAMP system demonstrated dramatically higher sensitivity while retaining the same specificity. Furthermore, we demonstrated concordant results between the two methods for the 126 clinical isolates.
Conclusion: Therefore, LAMP could be used for rapid identification of the five major carbapenemase gene families in routine clinical laboratories.
Keywords: carbapenemase-producing Enterobacteriaceae, loop-mediated isothermal amplification, bla NDM, bla KPC, bla VIM, bla IMP, bla OXA-48-like