Performance of Xpert Carba-R Assay for Identification of Carbapenemase Gene in the Clinical Microbiology Laboratory

Hae-Sun Chung, N. Yang, Y. Kim, Miae Lee, Sholhui Park
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Abstract

Objectives: The Xpert Carba-R Assay is a diagnostic test designed for the rapid detection and differentiation of the bla KPC , bla NDM , bla VIM , bla OXA-48 , and bla IMP-1 genes. We verified the performance of Xpert Carba-R Assay for identification of carbapenemase gene in the clinical microbiology laboratory. Methods: The analytical limit of detection was determined with two suspensions of carbapenemase-producing Enterobacteriaceae (CPE) isolates (KPC and NDM). A total of 52 specimens were evaluated: 21 bacterial isolates from clinical specimens, 21 rectal swabs, and 10 contrived stool specimens. Results: In bacterial isolates, concordant results between the Xpert Carba-R Assay and PCR were found in 20 of 21; 8 KPC, 8 NDM, 1 IMP, and 2 multiple carbapenamase genes (KPC/NDM, NDM/OXA) were detected both by Xpert Carba-R Assay and PCR. In one GES-positive isolate, Xpert Carba-R Assay showed a negative result as expected. One VIM-positive isolate tested negative by Xpert Carba-R Assay. Complete concordance was seen in rectal swab specimens: 4 specimens with KPC and 17 specimens with negative results both by Xpert Carba-R Assay and surveillance culture. Among the 10 contrived stool specimens, Xpert Carba-R Assay detected carbapenemase genes in 9 specimens as expected according to the CPE strains spiked into the contrived stool; 2 KPC, 4 NDM, 1 IMP, and 2 multiple carabapenamase genes (NDM/KPC, NDM/OXA). One VIM-positive specimen tested negative by Xpert Carba-R Assay. Conclusion: In conclusion, the Xpert Carba-R Assay can be used to identify carbapenemase gene in bacterial isolates cultured from clinical specimens and detect CPE carrier using rectal swab in clinical laboratories. (Ewha Med J 2020;43(3):39-42)
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Xpert碳- r法鉴定碳青霉烯酶基因在临床微生物实验室中的应用
目的:Xpert Carba-R检测是一种快速检测和分化bla KPC、bla NDM、bla VIM、bla OXA-48和bla IMP-1基因的诊断试验。我们在临床微生物实验室验证了Xpert碳青霉烯酶基因鉴定的性能。方法:采用产碳青霉烯酶肠杆菌科(CPE)分离株(KPC和NDM)两种悬液测定其检出限。共评估了52份标本:21份临床标本分离细菌,21份直肠拭子,10份人造粪便标本。结果:21株分离菌中有20株的Xpert Carba-R检测结果与PCR检测结果一致;采用Xpert Carba-R法和PCR检测8个KPC、8个NDM、1个IMP和2个多重碳青霉烯酶基因(KPC/NDM、NDM/OXA)。在一个ges阳性分离物中,Xpert Carba-R检测结果如预期的那样呈阴性。一个vim阳性分离物经Xpert Carba-R试验检测为阴性。直肠拭子标本完全一致:4例标本为KPC, 17例标本经Xpert Carba-R检测和监测培养均为阴性。在10份人造粪便标本中,Xpert Carba-R法检测到9份标本中碳青霉烯酶基因,根据添加到人造粪便中的CPE菌株进行检测;2个KPC基因,4个NDM基因,1个IMP基因,2个多重carabapenamase基因(NDM/KPC, NDM/OXA)。1例vim阳性标本经Xpert Carba-R试验呈阴性。结论:Xpert Carba-R法可用于临床标本培养细菌分离株碳青霉烯酶基因的鉴定,也可用于临床实验室直肠拭子检测CPE携带者。(梨花医学杂志2020;43(3):39-42)
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