利用基质辅助激光解吸电离飞行时间质谱法直接从阳性血液培养物中检测肠杆菌对碳青霉烯类的耐药性

Natália Kehl Moreira, Camila Mörschbächer Wilhelm, Fabiana Caroline Zempulski Volpato, Afonso Luís Barth, Juliana Caierão
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引用次数: 0

摘要

背景耐碳青霉烯类肠杆菌在全球范围内传播,与发病率和死亡率较高的感染有关。基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)是临床微生物实验室直接从血液培养物中鉴定病原体的有效工具。此外,它还被用于通过评估碳青霉烯水解作用来检测碳青霉烯酶的产生:确定美罗培南的水解度,直接从阳性血液培养物中检测碳青霉烯酶的产生,使用 logRQ 确定水解度的定量指标:我们评估了阳性血液培养物中的 100 种肠杆菌,其中 81 种携带碳青霉烯酶基因(blaKPC、blaGES、blaNDM-1、blaIMP、blaVIM 和 blaOXA-48-like),并通过实时多聚酶链反应和高分辨率熔解(HRM-qPCR)进行了测定。从阳性血培养瓶中提取的细菌蛋白质在美罗培南溶液中培养(2-4 小时)后离心,进行 MALDI-TOF MS 分析。水解和非水解形式的峰强度用于计算 logRQ 值:总体而言,灵敏度为 86.8%,特异性为 89.5%。值得注意的是,灵敏度因酶的类型而异。对于 blaKPC 阳性的分离物,灵敏度为 97.9%,而对于 blaNDM-1 和 blaOXA-48 样分离物,灵敏度明显降低:分别为 62.5%(16 个中的 10 个)和 66.7%(9 个中的 6 个)。事实上,blaKPC 阳性分离物的 logRQ(0.37-1.97)高于 blaNDM-1(-1.37 至 0.83)和 blaOXA-48 样分离物(-1.08 至 1.79):结论:这是一种直接从血培养瓶中鉴定碳青霉烯酶活性的廉价而快速的检测方法,有助于及早进行适当的抗菌治疗和实施感染控制措施。
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Detection of Carbapenem Resistance in Enterobacterales Directly From Positive Blood Cultures Using Matrix-Assisted Laser Desorption Ionization Time-of-Flight Mass Spectrometry.

Context.—: Carbapenem-resistant Enterobacterales are disseminated worldwide and associated with infections with high rates of morbidity and mortality. Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) is a useful tool for identification of pathogens directly from blood cultures in clinical microbiology laboratories. Furthermore, it has been applied for the detection of carbapenemase production, by evaluating carbapenem hydrolysis.

Objective.—: To determine meropenem hydrolysis to detect carbapenemase production directly from positive blood cultures, using logRQ to establish a quantitative measure of hydrolysis.

Design.—: We evaluated 100 Enterobacterales from positive blood cultures, with 81 carrying a carbapenemase gene (blaKPC, blaGES, blaNDM-1, blaIMP, blaVIM, and blaOXA-48-like), as determined by real-time multiplex polymerase chain reaction with high-resolution melting (HRM-qPCR). Bacterial proteins extracted from positive blood culture bottles were incubated in a meropenem solution (2-4 hours) followed by centrifugation for MALDI-TOF MS analysis. The intensity of peaks of the hydrolyzed and nonhydrolyzed forms were used to calculate the logRQ value.

Results.—: Overall, sensitivity was 86.8% and specificity, 89.5%. Of note, sensitivity varied depending on enzyme type. For blaKPC-positive isolates, sensitivity was 97.9%, while it reduced significantly for blaNDM-1 and blaOXA-48-like isolates: 62.5% (10 of 16) and 66.7% (6 of 9), respectively. Indeed, logRQ was higher in blaKPC-positive isolates (0.37-1.97) than in blaNDM-1 (-1.37 to 0.83) and blaOXA-48-like isolates (-1.08 to 1.79).

Conclusions.—: This is an inexpensive and rapid test to identify carbapenemase activity directly from blood culture bottles, which contributes to early adequate antimicrobial therapy and implementation of infection control measures.

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