Neimark H, Mitchelmore D, Leach R H
Department of Microbiology and Immunology, Morse Institute for Molecular Biology, State University of New York, Health Sciences Center at Brooklyn 11203, USA.
Int J Syst Bacteriol. 1998 Apr;48 Pt 2:389-94. doi: 10.1099/00207713-48-2-389.
An approach to characterizing uncultivated bacteria which combines a PFGE procedure for obtaining purified full-length chromosomes with PCR amplification is described. Isolated chromosomes from uncultivated organisms provide a specifically identifiable source material for hybridization, amplification and cloning. The availability of purified chromosomes for DNA amplification should aid in examining the diversity of microbial populations and should also reduce the possibility of forming hybrid DNA artifact molecules. The approach is illustrated by isolating the chromosome of the uncultivated agent of rodent Grey Lung disease and using the purified chromosomes to amplify and directly sequence the evolutionarily conserved 16S rRNA gene. The Grey Lung agent (GLA) contains a 650 kb chromosome and is shown to be a Mycoplasma sp. located phylogenetically in the hominis group of mycoplasmas. If a simple genomic lesion(s) is responsible for the unculturability of GLA, it is conceivable that complementation with DNA from a close relative could permit growth on artificial media.
描述了一种表征未培养细菌的方法,该方法将用于获得纯化全长染色体的脉冲场凝胶电泳(PFGE)程序与聚合酶链反应(PCR)扩增相结合。从未培养生物中分离出的染色体为杂交、扩增和克隆提供了一种可特异性识别的源材料。用于DNA扩增的纯化染色体的可用性应有助于检查微生物种群的多样性,也应降低形成杂交DNA假象分子的可能性。通过分离啮齿动物灰肺病未培养病原体的染色体,并使用纯化的染色体扩增和直接测序进化上保守的16S rRNA基因,来说明该方法。灰肺病病原体(GLA)含有一条650 kb的染色体,被证明是一种支原体,在系统发育上位于人型支原体组中。如果一个简单的基因组损伤导致了GLA的不可培养性,可以想象,与近亲的DNA互补可能允许在人工培养基上生长。