Hongoh Yuichi, Toyoda Atsushi
Department of Biological Sciences, Graduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, Tokyo, Japan.
Methods Mol Biol. 2011;733:25-33. doi: 10.1007/978-1-61779-089-8_2.
More than 99% of microorganisms on the earth are unculturable with known culturing techniques. The emergence of metagenomics with high-throughput sequencing technologies has enabled researchers to capture a comprehensive view of a complex bacterial community which comprises both culturable and unculturable species. However, the function of an individual species remains difficult to elucidate in a conventional metagenomic study, which generates numerous genomic fragments of unidentifiable origins at a species or genus level. This limitation hampers any in-depth investigations of the community and its unculturable bacterial members. Recently, as an alternative or compensatory approach, genomics targeting a single unculturable bacterial species in a complex community has been proposed. In this approach, whole-genome amplification technique using Phi29 DNA polymerase is applied to obtain a sufficient quantity of DNA for genome sequence analysis from only a single to a thousand bacterial cells. It is expected that a combination of the conventional metagenomics and this single-species-targeting genomics provides a great progress in understanding of the ecology, physiology, and evolution of unculturable microbial communities.
地球上超过99%的微生物无法用已知的培养技术进行培养。宏基因组学与高通量测序技术的出现,使研究人员能够全面了解一个复杂的细菌群落,其中包括可培养和不可培养的物种。然而,在传统的宏基因组学研究中,单个物种的功能仍然难以阐明,这种研究在物种或属水平上产生了大量来源不明的基因组片段。这一局限性阻碍了对该群落及其不可培养细菌成员的任何深入研究。最近,作为一种替代或补充方法,有人提出了针对复杂群落中单个不可培养细菌物种的基因组学。在这种方法中,应用使用Phi29 DNA聚合酶的全基因组扩增技术,从仅一到一千个细菌细胞中获得足够数量的DNA用于基因组序列分析。预计传统宏基因组学与这种单物种靶向基因组学的结合将在理解不可培养微生物群落的生态、生理和进化方面取得巨大进展。