Juvonen Riikka, Koivula Teija, Haikara Auli
VTT, P.O. Box 1000, FI-02044 VTT, Finland.
Int J Food Microbiol. 2008 Jul 15;125(2):162-9. doi: 10.1016/j.ijfoodmicro.2008.03.042. Epub 2008 Apr 7.
The strictly anaerobic brewery contaminants of the genera Pectinatus, Megasphaera, Selenomonas and Zymophilus in the class Clostridia constitute an important group of spoilage bacteria of unpasteurised, packaged beers. The aim of this study was to develop and evaluate group-specific PCR methods to detect and differentiate these bacteria in beer. A group-specific primer pair targeting a 342-bp variable region of the 16S rRNA gene was designed and evaluated in end-point PCR with gel electrophoresis and in real-time PCR with SYBR Green I dye. Significant cross-reactions with DNAs from any of the forty-two brewery-related, non-target microbes or from real brewery samples were not detected in either PCR system. The group-specific end-point and real-time PCR products could be differentiated according to species/genus and spoilage potential using restriction fragment length polymorphism (KpnI, XmnI, BssHII, ScaI) and melting point curve analysis, respectively. In combination with a rapid DNA extraction method, the PCR reactions detected ca 10(0)-10(3) CFU per 25 ml of beer depending on the strain and on the PCR system. The end-point and real-time PCR analysis took 6-7 h and 2-3 h, respectively. Pre-PCR enrichment of beer samples for 1-3 days ensured the detection of even a single cultivable cell. The PCR and cultivation results of real brewery samples were mostly congruent but the PCR methods were occasionally more sensitive. The PCR methods developed allow the detection of all the nine beer-spoilage Pectinatus, Megasphaera, Selenomonas and Zymophilus species in a single reaction and their differentiation below group level and reduce the analysis time for testing of their presence in beer samples by 1-2 days. The methods can be applied for brewery routine quality control and for studying occurrence, diversity and numbers of the strictly anaerobic beer spoilers in the brewing process.
梭菌纲中的果胶杆菌属、巨球形菌属、月形单胞菌属和嗜发酵单胞菌属等严格厌氧的啤酒污染物,是未巴氏杀菌包装啤酒中一类重要的腐败细菌。本研究的目的是开发和评估用于检测和区分啤酒中这些细菌的属特异性PCR方法。设计了一对靶向16S rRNA基因342 bp可变区的属特异性引物对,并在凝胶电泳终点PCR和SYBR Green I染料实时PCR中进行评估。在任一PCR系统中均未检测到与42种啤酒相关非靶标微生物的DNA或实际啤酒样品的DNA发生明显交叉反应。属特异性终点PCR产物和实时PCR产物可分别使用限制性片段长度多态性分析(KpnI、XmnI、BssHII、ScaI)和熔解曲线分析,根据物种/属和腐败潜力进行区分。结合快速DNA提取方法,根据菌株和PCR系统的不同,PCR反应每25 ml啤酒可检测到约10⁰-10³ CFU。终点PCR分析和实时PCR分析分别耗时6-7小时和2-3小时。啤酒样品预PCR富集1-3天可确保检测到单个可培养细胞。实际啤酒样品的PCR和培养结果大多一致,但PCR方法偶尔更灵敏。所开发的PCR方法可在单一反应中检测到所有九种导致啤酒变质的果胶杆菌属、巨球形菌属、月形单胞菌属和嗜发酵单胞菌属细菌,并在属以下水平进行区分,将检测啤酒样品中这些细菌存在的分析时间缩短1-2天。这些方法可用于啤酒厂常规质量控制,以及研究酿造过程中严格厌氧啤酒腐败菌的发生、多样性和数量。