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布鲁克基质辅助激光解吸电离生物分型CA系统用于临床需氧革兰氏阴性菌分离株鉴定的多中心评估

Multicenter Evaluation of the Bruker MALDI Biotyper CA System for the Identification of Clinical Aerobic Gram-Negative Bacterial Isolates.

作者信息

Faron Matthew L, Buchan Blake W, Hyke Josh, Madisen Neil, Lillie Jennifer L, Granato Paul A, Wilson Deborah A, Procop Gary W, Novak-Weekley Susan, Marlowe Elizabeth, Cumpio Joven, Griego-Fullbright Christen, Kindig Sandra, Timm Karen, Young Stephen, Ledeboer Nathan A

机构信息

Medical College of Wisconsin, Milwaukee, WI, United States of America.

Medical College of Wisconsin, Milwaukee, WI, United States of America; Wisconsin Diagnostic Laboratory, Milwaukee, WI, United States of America.

出版信息

PLoS One. 2015 Nov 3;10(11):e0141350. doi: 10.1371/journal.pone.0141350. eCollection 2015.

Abstract

The prompt and accurate identification of bacterial pathogens is fundamental to patient health and outcome. Recent advances in matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) have revolutionized bacterial identification in the clinical laboratory, but uniform incorporation of this technology in the U.S. market has been delayed by a lack of FDA-cleared systems. In this study, we conducted a multicenter evaluation of the MALDI Biotyper CA (MBT-CA) System (Bruker Daltonics Inc, Billerica, MA) for the identification of aerobic gram-negative bacteria as part of a 510(k) submission to the FDA. A total of 2,263 aerobic gram negative bacterial isolates were tested representing 23 genera and 61 species. Isolates were collected from various clinical sources and results obtained from the MBT-CA System were compared to DNA sequencing and/or biochemical testing. Isolates that failed to report as a "high confidence species ID" [log(score) ≥2.00] were re-tested using an extraction method. The MBT-CA System identified 96.8% and 3.1% of isolates with either a "high confidence" or a "low confidence" [log(score) value between 1.70 and <2.00] species ID, respectively. Two isolates did not produce acceptable confidence scores after extraction. The MBT-CA System correctly identified 99.8% (2,258/2,263) to genus and 98.2% (2,222/2,263) to species level. These data demonstrate that the MBT-CA System provides accurate results for the identification of aerobic gram-negative bacteria.

摘要

快速准确地鉴定细菌病原体对患者的健康和预后至关重要。基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF MS)的最新进展彻底改变了临床实验室中的细菌鉴定方法,但由于缺乏美国食品药品监督管理局(FDA)批准的系统,该技术在美国市场的统一应用有所延迟。在本研究中,我们对MALDI Biotyper CA(MBT-CA)系统(布鲁克道尔顿公司,马萨诸塞州比勒里卡)进行了多中心评估,以鉴定需氧革兰氏阴性菌,这是向FDA提交的510(k)申请的一部分。共测试了2263株需氧革兰氏阴性菌分离株,代表23个属和61个种。分离株从各种临床来源收集,并将MBT-CA系统获得的结果与DNA测序和/或生化测试结果进行比较。对于未报告为“高置信度物种鉴定”[对数(分数)≥2.00]的分离株,使用一种提取方法进行重新测试。MBT-CA系统分别以“高置信度”或“低置信度”[对数(分数)值在1.70至<2.00之间]鉴定出96.8%和3.1%的分离株。有两株分离株在提取后未产生可接受的置信度分数。MBT-CA系统在属水平上正确鉴定率为99.8%(2258/2263),在种水平上正确鉴定率为98.2%(2222/2263)。这些数据表明,MBT-CA系统为需氧革兰氏阴性菌的鉴定提供了准确的结果。

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