Dewhirst Floyd E, Shen Zeli, Scimeca Michael S, Stokes Lauren N, Boumenna Tahani, Chen Tsute, Paster Bruce J, Fox James G
Department of Molecular Genetics, The Forsyth Institute, Boston, Massachusetts 02115, USA.
J Bacteriol. 2005 Sep;187(17):6106-18. doi: 10.1128/JB.187.17.6106-6118.2005.
Analysis of 16S rRNA gene sequences has become the primary method for determining prokaryotic phylogeny. Phylogeny is currently the basis for prokaryotic systematics. Therefore, the validity of 16S rRNA gene-based phylogenetic analyses is of fundamental importance for prokaryotic systematics. Discrepancies between 16S rRNA gene analyses and DNA-DNA hybridization and phenotypic analyses have been noted in the genus Helicobacter. To clarify these discrepancies, we sequenced the 23S rRNA genes for 55 helicobacter strains representing 41 taxa (>2,700 bases per sequence). Phylogenetic-tree construction using neighbor-joining, parsimony, and maximum likelihood methods for 23S rRNA gene sequence data yielded stable trees which were consistent with other phenotypic and genotypic methods. The 16S rRNA gene sequence-derived trees were discordant with the 23S rRNA gene trees and other data. Discrepant 16S rRNA gene sequence data for the helicobacters are consistent with the horizontal transfer of 16S rRNA gene fragments and the creation of mosaic molecules with loss of phylogenetic information. These results suggest that taxonomic decisions must be supported by other phylogenetically informative macromolecules, such as the 23S rRNA gene, when 16S rRNA gene-derived phylogeny is discordant with other credible phenotypic and genotypic methods. This study found Wolinella succinogenes to branch with the unsheathed-flagellum cluster of helicobacters by 23S rRNA gene analyses and whole-genome comparisons. This study also found intervening sequences (IVSs) in the 23S rRNA genes of strains of 12 Helicobacter species. IVSs were found in helices 10, 25, and 45, as well as between helices 31' and 27'. Simultaneous insertion of IVSs at three sites was found in H. mesocricetorum.
16S rRNA基因序列分析已成为确定原核生物系统发育的主要方法。系统发育目前是原核生物分类学的基础。因此,基于16S rRNA基因的系统发育分析的有效性对于原核生物分类学至关重要。在幽门螺杆菌属中,已注意到16S rRNA基因分析与DNA-DNA杂交及表型分析之间存在差异。为了阐明这些差异,我们对代表41个分类单元的55株幽门螺杆菌菌株的23S rRNA基因进行了测序(每个序列>2700个碱基)。使用邻接法、简约法和最大似然法对23S rRNA基因序列数据构建系统发育树,得到了稳定的树,这些树与其他表型和基因型方法一致。由16S rRNA基因序列推导的树与23S rRNA基因树及其他数据不一致。幽门螺杆菌16S rRNA基因序列数据的差异与16S rRNA基因片段的水平转移以及具有系统发育信息丢失的镶嵌分子的产生是一致的。这些结果表明,当基于16S rRNA基因的系统发育与其他可靠的表型和基因型方法不一致时,分类学决策必须得到其他系统发育信息丰富的大分子(如23S rRNA基因)的支持。本研究通过23S rRNA基因分析和全基因组比较发现,产琥珀酸沃林氏菌与无鞘鞭毛的幽门螺杆菌簇分支。本研究还在12种幽门螺杆菌菌株的23S rRNA基因中发现了间隔序列(IVS)。在螺旋10、25和45以及螺旋31'和27'之间发现了IVS。在中仓鼠幽门螺杆菌中发现了三个位点同时插入IVS的情况。