Merck Millipore, Lab Solutions Business Unit, Biomonitoring R&D, 39 Route Industrielle de la Hardt, F-67120 Molsheim, France.
Merck Millipore, Lab Solutions Business Unit, Biomonitoring R&D, 39 Route Industrielle de la Hardt, F-67120 Molsheim, France.
J Microbiol Methods. 2014 Apr;99:71-80. doi: 10.1016/j.mimet.2014.02.004. Epub 2014 Feb 16.
Rapid detection methods for microbiological contamination are requested by many industries that respond to public health concerns. The control laboratories are replacing traditional culturing methods with faster assays based on nucleic acid amplification technologies, such as real-time PCR. However, an optimal nucleic acid sample preparation method is critical for the sensitivity and specificity of such tools. A high-throughput automated external ultrasonic device was developed for rapid lysing of microorganisms. Based on Ct values obtained from real-time PCR, there was efficient DNA release from the 16 microorganisms tested, including Gram positive and negative bacteria, bacterial spores, yeasts and spores of molds. Linearity of the lysis method was also demonstrated for Staphylococcus aureus, Pseudomonas aeruginosa, Salmonella enterica, Candida albicans and the spores of Aspergillus brasiliensis, with correlation coefficients (r(2)) between 0.90 and 0.98. After sonication, PCR analysis of the lysates revealed earlier Ct values (0.83 to 7.49) for S. aureus, P. aeruginosa and S. enterica compared to the bead-beating method of lysis. These results demonstrated more efficient DNA release from bacteria with the ultrasonication system. Nevertheless, for fungi, the Ct values were 0.94 to 1.61 later for sonication than for bead beating. This study demonstrates that 4min of sonication with this new automated high-throughput instrument allows for the efficient lysis of a large range of microorganisms.
许多对公众健康问题做出响应的行业都需要快速检测微生物污染的方法。控制实验室正在用基于核酸扩增技术(如实时 PCR)的更快检测方法取代传统的培养方法。然而,对于这些工具的灵敏度和特异性来说,一个最佳的核酸样品制备方法是至关重要的。一种高通量自动化外部超声设备被开发出来,用于快速裂解微生物。基于实时 PCR 获得的 Ct 值,从测试的 16 种微生物中(包括革兰氏阳性和阴性细菌、细菌孢子、酵母和霉菌孢子),都能有效地释放 DNA。还证明了该裂解方法对金黄色葡萄球菌、铜绿假单胞菌、肠炎沙门氏菌、白色念珠菌和巴西曲霉孢子的线性,相关系数(r(2))在 0.90 到 0.98 之间。超声处理后,对裂解物进行 PCR 分析显示,与珠磨法相比,金黄色葡萄球菌、铜绿假单胞菌和肠炎沙门氏菌的 Ct 值更早(0.83 到 7.49)。这些结果表明,与超声系统相比,该细菌的 DNA 释放更有效。然而,对于真菌,与珠磨法相比,超声处理的 Ct 值晚 0.94 到 1.61。本研究表明,使用这种新的自动化高通量仪器进行 4 分钟的超声处理可以有效地裂解大范围的微生物。