Holland Ricky D, Wilkes Jon G, Cooper Willie M, Alusta Pierre, Williams Anna, Pearce Bruce, Beaudoin Michael, Buzatu Dan
Division of Systems Biology/Innovative Safety and Technologies Branch, USFDA/National Center for Toxicological Research, 3900 NCTR Road, Jefferson, AR, 72079, USA.
Rapid Commun Mass Spectrom. 2014 Dec 15;28(23):2617-26. doi: 10.1002/rcm.7060.
The identification of bacteria based on mass spectra produced by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOFMS) has become routine since its introduction in 1996. The major drawback is that bacterial patterns produced by MALDI are dependent on sample preparation prior to analysis. This results in poor reproducibility in identifying bacterial types and between laboratories. The need for a more broadly applicable and useful sample handling procedure is warranted.
Thymol was added to the suspension solvent of bacteria prior to MALDI analysis. The suspension solvent consisted of ethanol, water and TFA. The bacterium was added to the thymol suspension solvent and heated. An aliquot of the bacterial suspension was mixed directly with the matrix solution at a 9:1 ratio, matrix/bacteria solution, respectively. The mixture was then placed on the MALDI plate and allowed to air dry before MALDI analysis.
The thymol method improved the quality of spectra and number of peaks when compared to other sample preparation procedures studied. The bacterium-identifying biomarkers assigned to four strains of E. coli were statistically 95% reproducible analyzed on three separate days. The thymol method successfully differentiated between the four E. coli strains. In addition, the thymol procedure could identify nine out of ten S. enterica serovars over a 3-day period and nine S. Typhimurium strains from the other ten serovars 90% of the time over the same period.
The thymol method can identify certain bacteria at the sub-species level and yield reproducible results over time. It improves the quality of spectra by increasing the number of peaks when compared to the other sample preparation methods assessed in this study. Published in 2014. This article is a U.S. Government work and is in the public domain in the USA.
自1996年基质辅助激光解吸/电离飞行时间质谱(MALDI-TOFMS)引入以来,基于其产生的质谱图鉴定细菌已成为常规方法。主要缺点是MALDI产生的细菌图谱依赖于分析前的样品制备。这导致在鉴定细菌类型以及不同实验室之间的重现性较差。因此,需要一种更广泛适用且有用的样品处理程序。
在进行MALDI分析之前,将百里酚添加到细菌的悬浮溶剂中。悬浮溶剂由乙醇、水和三氟乙酸组成。将细菌添加到百里酚悬浮溶剂中并加热。取一份细菌悬浮液,分别以9:1的比例与基质溶液直接混合,即基质/细菌溶液。然后将混合物置于MALDI板上,在进行MALDI分析前让其空气干燥。
与所研究的其他样品制备程序相比,百里酚方法提高了光谱质量和峰数量。在三个不同日期对四株大肠杆菌进行分析时,鉴定细菌的生物标志物在统计学上有95%的重现性。百里酚方法成功区分了这四株大肠杆菌。此外,在三天时间内,百里酚程序能够鉴定出十分之九的肠炎沙门氏菌血清型,并且在同一时期内,能90%的时间鉴定出其他十种血清型中的九株鼠伤寒沙门氏菌菌株。
百里酚方法可以在亚种水平上鉴定某些细菌,并随着时间推移产生可重现的结果。与本研究中评估的其他样品制备方法相比,它通过增加峰数量提高了光谱质量。2014年发表。本文是美国政府作品,在美国属于公共领域。