Archaea Centre, Department of Biology, Copenhagen University, Ole Maaløes Vej 5, DK-2200 Copenhagen N, Denmark.
Environ Microbiol. 2010 Nov;12(11):2918-30. doi: 10.1111/j.1462-2920.2010.02266.x.
Two novel viral genomes and four plasmids were assembled from an environmental sample collected from a hot spring at Yellowstone National Park, USA, and maintained anaerobically in a bioreactor at 85°C and pH 6. The double-stranded DNA viral genomes are linear (22.7 kb) and circular (17.7 kb), and derive apparently from archaeal viruses HAV1 and HAV2. Genomic DNA was obtained from samples enriched in filamentous and tadpole-shaped virus-like particles respectively. They yielded few significant matches in public sequence databases reinforcing, further, the wide diversity of archaeal viruses. Several variants of HAV1 exhibit major genomic alterations, presumed to arise from viral adaptation to different hosts. They include insertions up to 350 bp, deletions up to 1.5 kb, and genes with extensively altered sequences. Some result from recombination events occurring at low complexity direct repeats distributed along the genome. In addition, a 33.8 kb archaeal plasmid pHA1 was characterized, encoding a possible conjugative apparatus, as well as three cryptic plasmids of thermophilic bacterial origin, pHB1 of 2.1 kb and two closely related variants pHB2a and pHB2b, of 5.2 and 4.8 kb respectively. Strategies are considered for assembling genomes of smaller genetic elements from complex environmental samples, and for establishing possible host identities on the basis of sequence similarity to host CRISPR immune systems.
从美国黄石国家公园温泉采集的环境样本中,通过组装,得到了两个新的病毒基因组和四个质粒,这些样本在 85°C 和 pH6 的生物反应器中保持厌氧状态。双链 DNA 病毒基因组是线性的(22.7kb)和环形的(17.7kb),显然来源于古菌病毒 HAV1 和 HAV2。从分别富含丝状和蝌蚪状病毒样颗粒的样本中获得了基因组 DNA。它们在公共序列数据库中的匹配度很低,这进一步证明了古菌病毒的广泛多样性。几种 HAV1 变体表现出主要的基因组改变,据推测是病毒适应不同宿主的结果。这些改变包括长达 350bp 的插入、长达 1.5kb 的缺失以及序列广泛改变的基因。其中一些是由沿着基因组分布的低复杂度直接重复序列发生重组事件引起的。此外,还对一个 33.8kb 的古菌质粒 pHA1 进行了表征,该质粒编码了一个可能的共轭装置,以及三个源自嗜热细菌的隐性质粒 pHB1(2.1kb)和两个密切相关的变体 pHB2a 和 pHB2b(分别为 5.2kb 和 4.8kb)。还考虑了从复杂环境样本中组装较小遗传元件基因组的策略,以及基于与宿主 CRISPR 免疫系统的序列相似性确定可能宿主身份的策略。