Ghebremedhin B, Layer F, König W, König B
Otto-von-Guericke University, Clinical Microbiology, Leipziger Str. 44, Magdeburg, Germany.
J Clin Microbiol. 2008 Mar;46(3):1019-25. doi: 10.1128/JCM.02058-07. Epub 2008 Jan 3.
The analysis of 16S rRNA gene sequences has been the technique generally used to study the evolution and taxonomy of staphylococci. However, the results of this method do not correspond to the results of polyphasic taxonomy, and the related species cannot always be distinguished from each other. Thus, new phylogenetic markers for Staphylococcus spp. are needed. We partially sequenced the gap gene (approximately 931 bp), which encodes the glyceraldehyde-3-phosphate dehydrogenase, for 27 Staphylococcus species. The partial sequences had 24.3 to 96% interspecies homology and were useful in the identification of staphylococcal species (F. Layer, B. Ghebremedhin, W. König, and B. König, J. Microbiol. Methods 70:542-549, 2007). The DNA sequence similarities of the partial staphylococcal gap sequences were found to be lower than those of 16S rRNA (approximately 97%), rpoB (approximately 86%), hsp60 (approximately 82%), and sodA (approximately 78%). Phylogenetically derived trees revealed four statistically supported groups: S. hyicus/S. intermedius, S. sciuri, S. haemolyticus/S. simulans, and S. aureus/epidermidis. The branching of S. auricularis, S. cohnii subsp. cohnii, and the heterogeneous S. saprophyticus group, comprising S. saprophyticus subsp. saprophyticus and S. equorum subsp. equorum, was not reliable. Thus, the phylogenetic analysis based on the gap gene sequences revealed similarities between the dendrograms based on other gene sequences (e.g., the S. hyicus/S. intermedius and S. sciuri groups) as well as differences, e.g., the grouping of S. arlettae and S. kloosii in the gap-based tree. From our results, we propose the partial sequencing of the gap gene as an alternative molecular tool for the taxonomical analysis of Staphylococcus species and for decreasing the possibility of misidentification.
16S rRNA基因序列分析一直是研究葡萄球菌进化和分类的常用技术。然而,该方法的结果与多相分类法的结果不一致,相关物种之间往往无法相互区分。因此,需要新的葡萄球菌系统发育标记。我们对27种葡萄球菌的gap基因(约931 bp)进行了部分测序,该基因编码甘油醛-3-磷酸脱氢酶。部分序列的种间同源性为24.3%至96%,可用于葡萄球菌物种的鉴定(F. Layer、B. Ghebremedhin、W. König和B. König,《微生物学方法杂志》70:542 - 549,2007年)。发现葡萄球菌gap部分序列的DNA序列相似性低于16S rRNA(约97%)、rpoB(约86%)、hsp60(约82%)和sodA(约78%)。系统发育树显示出四个有统计学支持的组:猪葡萄球菌/中间葡萄球菌、松鼠葡萄球菌、溶血葡萄球菌/模仿葡萄球菌以及金黄色葡萄球菌/表皮葡萄球菌。耳葡萄球菌、科氏葡萄球菌科氏亚种以及由腐生葡萄球菌腐生亚种和马胃葡萄球菌马胃亚种组成的异质腐生葡萄球菌组的分支不可靠。因此,基于gap基因序列的系统发育分析揭示了基于其他基因序列的树状图之间的相似性(例如猪葡萄球菌/中间葡萄球菌和松鼠葡萄球菌组)以及差异,例如在基于gap的树状图中阿氏葡萄球菌和克氏葡萄球菌的分组。根据我们的结果,我们建议将gap基因的部分测序作为葡萄球菌物种分类分析的替代分子工具,并降低错误鉴定的可能性。