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采用实时 PCR 和熔解曲线分析快速检测肠杆菌科和革兰氏阴性非发酵菌中的 IMP、NDM、VIM、KPC 和 OXA-48 样碳青霉烯酶。

Rapid detection of IMP, NDM, VIM, KPC and OXA-48-like carbapenemases from Enterobacteriales and Gram-negative non-fermenter bacteria by real-time PCR and melt-curve analysis.

机构信息

Specialist Antimicrobial and Chemotherapy Unit, Public Health Wales, University Hospital of Wales, Heath Park, Cardiff, CF14 4XW, UK.

School of Medicine, Cardiff University, Heath Park, Cardiff, CF14 4XN, UK.

出版信息

Eur J Clin Microbiol Infect Dis. 2019 Nov;38(11):2029-2036. doi: 10.1007/s10096-019-03637-5. Epub 2019 Aug 5.

Abstract

Carbapenemase-producing microorganisms are increasingly isolated and often associated with treatment failures and outbreaks. The need for reliable and timely detection and/or confirmation of carbapenemase production is paramount; therefore, a real-time PCR assay targeting IMP, NDM, VIM, KPC and OXA-48-like carbapenemases was designed and validated. All available allele variants of the above carbapenemases were downloaded from the Beta-Lactamase DataBase ( http://bldb.eu/ ), aligned with Clustal Omega and primers designed using Primer-BLAST. Real-time PCR monoplexes were optimized for the QuantStudio 6-Flex (Applied Biosystems) using the PowerUp SYBR Green Master Mix (Life Technologies) and validated using a panel of 204 characterised strains carrying a wide range of beta-lactamases, sometimes in combination. Melt-curve analysis was used to confirm positive results. The in silico approach allowed primers to be designed in conserved regions of the KPC and NDM alignments, while three primer sets for IMP and two for VIM were necessary to ensure amplification of the different variants. One primer set was designed for OXA-48-like; however, it is unlikely to detect all variants. Expected results were obtained for all 204 tested strains, with 100% sensitivity and specificity. Melt-curve analysis showed consistent Tm results for KPC, NDM, and OXA-48-like; differences were instead noted for IMP and VIM as likely consequence of higher variability in the PCR target regions. Inhibition was not observed. The assay is rapid, easy to perform and implement. It enables unequivocal detection of IMP, NDM, VIM, KPC and OXA-48-like carbapenemases even when more than one type is present simultaneously.

摘要

产碳青霉烯酶微生物的分离越来越多,并且常常与治疗失败和爆发有关。因此,迫切需要可靠和及时地检测和/或确认碳青霉烯酶的产生;因此,设计并验证了一种针对 IMP、NDM、VIM、KPC 和 OXA-48 样碳青霉烯酶的实时 PCR 检测方法。从 Beta-Lactamase DataBase(http://bldb.eu/)下载了上述碳青霉烯酶的所有可用等位基因变体,使用 Clustal Omega 进行比对,并使用 Primer-BLAST 设计引物。使用 QuantStudio 6-Flex(Applied Biosystems)使用 PowerUp SYBR Green Master Mix(Life Technologies)优化了实时 PCR 单重反应,并使用携带广泛的β-内酰胺酶的 204 个特征菌株进行了验证,有时是组合的。熔解曲线分析用于确认阳性结果。 基于序列比对的方法允许在 KPC 和 NDM 比对的保守区域设计引物,而 IMP 有三组引物和 VIM 有两组引物是确保扩增不同变体所必需的。设计了一组引物用于 OXA-48 样;然而,它不太可能检测到所有变体。对所有 204 个测试菌株都获得了预期的结果,具有 100%的灵敏度和特异性。熔解曲线分析显示 KPC、NDM 和 OXA-48 样的 Tm 结果一致;IMP 和 VIM 则存在差异,这可能是由于 PCR 靶区域的变异性更高所致。未观察到抑制。该检测方法快速、易于操作和实施。它能够明确检测到 IMP、NDM、VIM、KPC 和 OXA-48 样碳青霉烯酶,即使同时存在多种类型。

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