Department of Life and Nanopharmaceutical Sciences and Department of Biology, Kyung Hee University, Seoul, Republic of Korea.
ISME J. 2010 Jan;4(1):1-16. doi: 10.1038/ismej.2009.83. Epub 2009 Jul 9.
Little is known about the archaeal diversity of fermented seafood; most of the earlier studies of fermented food have focused on lactic acid bacteria (LAB) in the fermentation process. In this study, the archaeal and bacterial diversity in seven kinds of fermented seafood were culture-independently examined using barcoded pyrosequencing and PCR-denaturing gradient gel electrophoresis (DGGE) methods. The multiplex barcoded pyrosequencing was performed in a single run, with multiple samples tagged uniquely by multiplex identifiers, using different primers for Archaea or Bacteria. Because PCR-DGGE analysis is a conventional molecular ecological approach, this analysis was also performed on the same samples and the results were compared with the results of the barcoded pyrosequencing analysis. A total of 13 372 sequences were retrieved from 15 898 pyrosequencing reads and were analyzed to evaluate the diversity of the archaeal and bacterial populations in seafood. The most predominant types of archaea and bacteria identified in the samples included extremely halophilic archaea related to the family Halobacteriaceae; various uncultured mesophilic Crenarchaeota, including Crenarchaeota Group I.1 (CG I.1a and CG I.1b), Marine Benthic Group B (MBG-B), and Miscellaneous Crenarchaeotic Group (MCG); and LAB affiliated with genus Lactobacillus and Weissella. Interestingly, numerous uncultured mesophilic Crenarchaeota groups were as ubiquitous in the fermented seafood as in terrestrial and aquatic niches; the existence of these Crenarchaeota groups has not been reported in any fermented food. These results indicate that the archaeal populations in the fermented seafood analyzed are diverse and include the halophilic and mesophilic groups, and that barcoded pyrosequencing is a promising and cost-effective method for analyzing microbial diversity compared with conventional approaches.
关于发酵海产品的古菌多样性知之甚少;早期发酵食品的研究大多集中在发酵过程中的乳酸菌(LAB)上。在这项研究中,采用带有条形码的焦磷酸测序和 PCR-变性梯度凝胶电泳(DGGE)方法,对七种发酵海产品中的古菌和细菌多样性进行了非培养依赖性的检测。多重条形码焦磷酸测序是在一个单一的运行中进行的,使用不同的引物对古菌或细菌进行多重标记,通过多重标识符对多个样本进行标记。由于 PCR-DGGE 分析是一种常规的分子生态学方法,因此对相同的样本进行了此分析,并将结果与条形码焦磷酸测序分析的结果进行了比较。从 15898 个焦磷酸测序读数中获得了 13372 个序列,用于评估海产品中古菌和细菌种群的多样性。在样品中鉴定出的最主要的古菌和细菌类型包括与 Halobacteriaceae 科相关的极端嗜盐古菌;各种未培养的中温 Crenarchaeota,包括 Crenarchaeota Group I.1(CG I.1a 和 CG I.1b)、海洋底栖群 B(MBG-B)和 Miscellaneous Crenarchaeotic Group(MCG);以及与乳杆菌属和魏斯氏菌属相关的 LAB。有趣的是,许多未培养的中温 Crenarchaeota 群在发酵海产品中的普遍性与陆地和水生环境中的相似;在任何发酵食品中都没有报道过这些 Crenarchaeota 群的存在。这些结果表明,分析的发酵海产品中的古菌种群是多样的,包括嗜盐菌和中温菌,与传统方法相比,条形码焦磷酸测序是一种有前途且具有成本效益的微生物多样性分析方法。