Balding Claire, Bromley Stephen A, Pickup Roger W, Saunders Jon R
School of Biological Sciences, Biosciences Building, Crown Street, University of Liverpool, Liverpool L69 7ZB, UK.
Environ Microbiol. 2005 Oct;7(10):1558-67. doi: 10.1111/j.1462-2920.2005.00845.x.
Viruses are the most abundant biological entities in aquatic systems. Temperate bacteriophages have enormous influences on microbial diversity, genetic exchange and bacterial population dynamics. However, development of molecular tools for their detection in the environment has been problematic. The integrase gene is used here as a molecular marker to analyse the diversity of temperate bacteriophages in a population of freshwater bacteria. Interrogation of the GenBank database revealed 32 non-cryptic enteric phage integrase sequences, leading to the development of a suite of 11 degenerate primer sets specific to the extant sequences elucidated. Application of these primer sets to enterobacterial isolates recovered from a freshwater pond and the temperate phages induced from them revealed a number of diverse integrase genes, including novel integrase-like sequences not represented in the databases. This highlights the potential of utilizing the integrase gene family as a marker for phage diversity.
病毒是水生系统中数量最为丰富的生物实体。温和噬菌体对微生物多样性、基因交换和细菌种群动态有着巨大影响。然而,开发用于在环境中检测它们的分子工具一直存在问题。在此,整合酶基因被用作分子标记,以分析淡水细菌群体中温和噬菌体的多样性。对GenBank数据库的查询揭示了32个非隐秘性肠道噬菌体整合酶序列,从而开发出一套针对已阐明的现有序列的11个简并引物组。将这些引物组应用于从淡水池塘分离出的肠杆菌菌株以及从中诱导出的温和噬菌体,发现了许多不同的整合酶基因,包括数据库中未有的新型整合酶样序列。这凸显了利用整合酶基因家族作为噬菌体多样性标记的潜力。