Griffiths Emma, Petrich Astrid K, Gupta Radhey S
Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton L8N 3Z5, Canada.
Department of Pathology and Molecular Medicine, McMaster University, Hamilton L8N 3Z5, Canada.
Microbiology (Reading). 2005 Aug;151(Pt 8):2647-2657. doi: 10.1099/mic.0.28057-0.
All known chlamydiae are either proven human or animal pathogens or possess such potential. Due to increasing reports of chlamydiae diversity in the environment, it is important to develop reliable means for identifying and characterizing Chlamydiales species. The identification of environmental chlamydiae at present relies on their branching pattern in 16S rRNA trees, as well as 16S/23S consensus motifs which display variability. At present, no reliable molecular signatures are known which are unique to all Chlamydiales species. Besides the rRNAs, sequence information for different Chlamydiales is not available for any other gene sequence. In this report, a number of molecular signatures are described that consist of conserved inserts and deletions (indels), in widely distributed proteins [RNA polymerase alpha subunit (RpoA), elongation factor (EF)-Tu, EF-P, DNA gyrase B subunit (GyrB) and lysyl-tRNA synthetase (LysRS)], that are distinctive characteristics of all available chlamydiae homologues (from Chlamydiaeceae species and Parachlamydiae sp. UWE25) and not found in any other bacteria. Using PCR primers for highly conserved regions in these proteins, the corresponding fragments of these genes from Simkania negevensis, Waddlia chondrophila, and in a number of cases for Neochlamydia hartmanellae, covering all families within the phylum Chlamydiae, have been cloned and sequenced. The shared presence of the identified signatures in these species provides strong evidence that these molecular signatures are distinctive characteristics of the entire order Chlamydiales and can be used to reliably determine the presence of chlamydiae or chlamydia-related organisms in environmental samples. The sequence information for these protein fragments was also used to determine the interrelationships among chlamydiae species. In a phylogenetic tree based on a combined dataset of sequences from RpoA, EF-Tu, EF-P and GyrB, the environmental chlamydiae (i.e. Simkania, Waddlia and Parachlamydia) and the traditional Chlamydiaceae (i.e. Chlamydophila and Chlamydia) formed two distinct clades. Similar relationships were also observed in individual protein phylogenies, as well as in a 16S rRNA tree for the same species. These results provide evidence that the divergence between the traditional Chlamydiaceae species and the other chlamydiae families occurred very early in the evolution of this group of bacteria.
所有已知的衣原体要么已被证实是人类或动物病原体,要么具有这种潜在可能性。由于环境中衣原体多样性的报道日益增多,开发可靠的方法来鉴定和表征衣原体目物种非常重要。目前,环境衣原体的鉴定依赖于它们在16S rRNA树中的分支模式,以及显示出变异性的16S/23S共有基序。目前,还没有已知的对所有衣原体目物种都独特的可靠分子特征。除了rRNA外,没有任何其他基因序列可获取不同衣原体目的序列信息。在本报告中,描述了一些分子特征,这些特征由广泛分布的蛋白质[RNA聚合酶α亚基(RpoA)、延伸因子(EF)-Tu、EF-P、DNA促旋酶B亚基(GyrB)和赖氨酰-tRNA合成酶(LysRS)]中的保守插入和缺失(插入缺失)组成,是所有可用衣原体同源物(来自衣原体科物种和副衣原体属UWE25)的独特特征,在任何其他细菌中均未发现。使用针对这些蛋白质中高度保守区域的PCR引物,已克隆并测序了来自内格夫希曼尼亚菌、嗜软骨沃氏菌以及在许多情况下来自哈氏新衣原体的这些基因的相应片段,涵盖了衣原体门内的所有科。这些物种中所鉴定特征的共同存在提供了有力证据,表明这些分子特征是整个衣原体目的独特特征,可用于可靠地确定环境样本中衣原体或衣原体相关生物体的存在。这些蛋白质片段的序列信息也用于确定衣原体物种之间的相互关系。在基于RpoA、EF-Tu、EF-P和GyrB序列的组合数据集构建的系统发育树中,环境衣原体(即希曼尼亚菌、沃氏菌和副衣原体)和传统衣原体科(即嗜衣原体属和衣原体属)形成了两个不同的分支。在单个蛋白质系统发育以及相同物种的16S rRNA树中也观察到了类似的关系。这些结果提供了证据,表明传统衣原体科物种与其他衣原体科之间的分化发生在这组细菌进化的早期阶段。