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采用可变 16S rDNA 区域 DNA 高分辨率熔解分析快速鉴定乳中嗜温和嗜热芽孢形成菌。

Rapid identification of dairy mesophilic and thermophilic sporeforming bacteria using DNA high resolution melt analysis of variable 16S rDNA regions.

机构信息

School of Agriculture and Food Sciences, The University of Queensland, St. Lucia campus, Brisbane, Queensland 4072, Australia.

出版信息

Int J Food Microbiol. 2013 Jul 15;165(2):175-83. doi: 10.1016/j.ijfoodmicro.2013.05.007. Epub 2013 May 17.

DOI:10.1016/j.ijfoodmicro.2013.05.007
PMID:23743474
Abstract

Due to their ubiquity in the environment and ability to survive heating processes, sporeforming bacteria are commonly found in foods. This can lead to product spoilage if spores are present in sufficient numbers and where storage conditions favour spore germination and growth. A rapid method to identify the major aerobic sporeforming groups in dairy products, including Bacillus licheniformis group, Bacillus subtilis group, Bacillus pumilus group, Bacillus megaterium, Bacillus cereus group, Geobacillus species and Anoxybacillus flavithermus was devised. This method involves real-time PCR and high resolution melt analysis (HRMA) of V3 (70 bp) and V6 (100 bp) variable regions in the 16S rDNA. Comparisons of HRMA curves from 194 isolates of the above listed sporeforming bacteria obtained from dairy products which were identified using partial 16S rDNA sequencing, allowed the establishment of criteria for differentiating them from each other and several non-sporeforming bacteria found in samples. A blinded validation trial on 28 bacterial isolates demonstrated complete accuracy in unambiguous identification of the 7 different aerobic sporeformers. The reliability of HRMA method was also verified using boiled extractions of crude DNA, thereby shortening the time needed for identification. The HRMA method described in this study provides a new and rapid approach to identify the dominant mesophilic and thermophilic aerobic sporeforming bacteria found in a wide variety of dairy products.

摘要

由于其在环境中的普遍存在以及耐受加热过程的能力,芽孢形成菌通常存在于食品中。如果孢子数量充足,并且储存条件有利于孢子发芽和生长,那么它们就会导致产品变质。本研究开发了一种快速方法来鉴定乳制品中的主要需氧芽孢形成菌群,包括地衣芽孢杆菌群、枯草芽孢杆菌群、短小芽孢杆菌群、巨大芽孢杆菌、蜡样芽孢杆菌群、解淀粉芽孢杆菌属和嗜热脂肪芽孢杆菌。该方法涉及实时 PCR 和 16S rDNA 的 V3(70 bp)和 V6(100 bp)可变区的高分辨率熔解分析(HRMA)。对从乳制品中获得的 194 株上述芽孢形成菌的 HRMA 曲线进行比较,这些菌是通过部分 16S rDNA 测序鉴定的,允许建立区分它们彼此和样品中发现的几种非芽孢形成菌的标准。对 28 株细菌分离株进行的盲法验证试验表明,对 7 种不同好氧芽孢形成菌的明确鉴定具有完全准确性。使用煮沸的粗提 DNA 还验证了 HRMA 方法的可靠性,从而缩短了鉴定所需的时间。本研究中描述的 HRMA 方法为鉴定广泛存在于各种乳制品中的主要中温和耐热需氧芽孢形成菌提供了一种新的快速方法。

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