Pannekoek Yvonne, Morelli Giovanna, Kusecek Barica, Morré Servaas A, Ossewaarde Jacobus M, Langerak Ankie A, van der Ende Arie
Department of Medical Microbiology, Center for Infection and Immunity Amsterdam (CINIMA), Academic Medical Center, Amsterdam, The Netherlands.
BMC Microbiol. 2008 Feb 28;8:42. doi: 10.1186/1471-2180-8-42.
The obligate intracellular growing bacterium Chlamydia trachomatis causes diseases like trachoma, urogenital infection and lymphogranuloma venereum with severe morbidity. Several serovars and genotypes have been identified, but these could not be linked to clinical disease or outcome. The related Chlamydophila pneumoniae, of which no subtypes are recognized, causes respiratory infections worldwide. We developed a multi locus sequence typing (MLST) scheme to understand the population genetic structure and diversity of these species and to evaluate the association between genotype and disease.
A collection of 26 strains of C. trachomatis of different serovars and clinical presentation and 18 strains of C. pneumoniae were included in the study. For comparison, sequences of C. abortus, C. psittaci, C. caviae, C. felis, C. pecorum (Chlamydophila), C. muridarum (Chlamydia) and of Candidatus protochlamydia and Simkania negevensis were also included. Sequences of fragments (400 - 500 base pairs) from seven housekeeping genes (enoA, fumC, gatA, gidA, hemN, hlfX, oppA) were analysed. Analysis of allelic profiles by eBurst revealed three non-overlapping clonal complexes among the C. trachomatis strains, while the C. pneumoniae strains formed a single group. An UPGMA tree produced from the allelic profiles resulted in three groups of sequence types. The LGV strains grouped in a single cluster, while the urogenital strains were distributed over two separated groups, one consisted solely of strains with frequent occurring serovars (E, D and F). The distribution of the different serovars over the three groups was not consistent, suggesting exchange of serovar encoding ompA sequences. In one instance, exchange of fumC sequences between strains of different groups was observed. Cluster analyses of concatenated sequences of the Chlamydophila and Chlamydia species together with those of Candidatus Protochlamydia amoebophila and Simkania negevensis resulted in a tree identical to that obtained with 23S RNA gene sequences.
These data show that C. trachomatis and C. pneumoniae are highly uniform. The difference in genetic diversity between C. trachomatis and C. pneumoniae is in concordance with a later assimilation to the human host of the latter. Our data supports the taxonomy of the order of Chlamydiales.
专性细胞内生长的细菌沙眼衣原体可引发如沙眼、泌尿生殖系统感染及性病性淋巴肉芽肿等疾病,发病率很高。已鉴定出几种血清型和基因型,但它们与临床疾病或结局并无关联。相关的肺炎衣原体在全球范围内引发呼吸道感染,目前尚未发现其亚型。我们开发了一种多位点序列分型(MLST)方案,以了解这些物种的群体遗传结构和多样性,并评估基因型与疾病之间的关联。
本研究纳入了26株不同血清型和临床表现的沙眼衣原体菌株以及18株肺炎衣原体菌株。作为比较,还纳入了流产衣原体、鹦鹉热衣原体、豚鼠衣原体、猫衣原体、猪衣原体(嗜衣原体属)、鼠衣原体(衣原体属)以及嗜阿米巴原衣原体和内格夫希曼凯菌的序列。分析了来自7个管家基因(enoA、fumC、gatA、gidA、hemN、hlfX、oppA)的片段(400 - 500个碱基对)序列。通过eBurst分析等位基因谱发现,沙眼衣原体菌株中有三个不重叠的克隆复合体,而肺炎衣原体菌株形成一个单一组。根据等位基因谱构建的UPGMA树产生了三组序列类型。性病性淋巴肉芽肿菌株聚集在一个单一簇中,而泌尿生殖系统菌株分布在两个分开的组中,其中一组仅由常见血清型(E、D和F)的菌株组成。不同血清型在这三组中的分布不一致,这表明编码ompA序列的血清型发生了交换。在一个实例中,观察到不同组的菌株之间发生了fumC序列的交换。对嗜衣原体属和衣原体属物种以及嗜阿米巴原衣原体和内格夫希曼凯菌的串联序列进行聚类分析,得到的树与用23S RNA基因序列得到的树相同。
这些数据表明沙眼衣原体和肺炎衣原体高度一致。沙眼衣原体和肺炎衣原体在遗传多样性上的差异与后者对人类宿主的后期适应相一致。我们的数据支持衣原体目的分类学。