Schleper C, DeLong E F, Preston C M, Feldman R A, Wu K Y, Swanson R V
Marine Science Institute, University of California, Santa Barbara, California 93106, USA.
J Bacteriol. 1998 Oct;180(19):5003-9. doi: 10.1128/JB.180.19.5003-5009.1998.
Molecular phylogenetic surveys have recently revealed an ecologically widespread crenarchaeal group that inhabits cold and temperate terrestrial and marine environments. To date these organisms have resisted isolation in pure culture, and so their phenotypic and genotypic characteristics remain largely unknown. To characterize these archaea, and to extend methodological approaches for characterizing uncultivated microorganisms, we initiated genomic analyses of the nonthermophilic crenarchaeote Cenarchaeum symbiosum found living in association with a marine sponge, Axinella mexicana. Complex DNA libraries derived from the host-symbiont population yielded several large clones containing the ribosomal operon from C. symbiosum. Unexpectedly, cloning and sequence analysis revealed the presence of two closely related variants that were consistently found in the majority of host individuals analyzed. Homologous regions from the two variants were sequenced and compared in detail. The variants exhibit >99.2% sequence identity in both small- and large-subunit rRNA genes and they contain homologous protein-encoding genes in identical order and orientation over a 28-kbp overlapping region. Our study not only indicates the potential for characterizing uncultivated prokaryotes by genome sequencing but also identifies the primary complication inherent in the approach: the widespread genomic microheterogeneity in naturally occurring prokaryotic populations.
分子系统发育调查最近发现了一个在生态上广泛分布的泉古菌群体,它们栖息于寒冷和温带的陆地及海洋环境中。迄今为止,这些生物一直无法在纯培养中分离出来,因此它们的表型和基因型特征在很大程度上仍然未知。为了表征这些古菌,并扩展表征未培养微生物的方法,我们启动了对与海洋海绵墨西哥轴海绵共生生活的非嗜热泉古菌共生泉古菌的基因组分析。从宿主 - 共生体群体中获得的复杂DNA文库产生了几个包含共生泉古菌核糖体操纵子的大克隆。出乎意料的是,克隆和序列分析揭示了在大多数分析的宿主个体中一致存在的两个密切相关的变体。对这两个变体的同源区域进行了测序并详细比较。这两个变体在小亚基和大亚基rRNA基因中均表现出>99.2%的序列同一性,并且它们在一个28千碱基对的重叠区域中以相同的顺序和方向包含同源蛋白质编码基因。我们的研究不仅表明了通过基因组测序表征未培养原核生物的潜力,而且还确定了该方法固有的主要复杂性:自然存在的原核生物群体中广泛存在的基因组微异质性。