Global and Tropical Health Division, Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.
School of Psychological and Clinical Sciences, Charles Darwin University, Darwin, Northern Territory, Australia.
PLoS One. 2018 Apr 10;13(4):e0195454. doi: 10.1371/journal.pone.0195454. eCollection 2018.
Chlamydia trachomatis infects the urogenital tract (UGT) and eyes. Anatomical tropism is correlated with variation in the major outer membrane protein encoded by ompA. Strains possessing the ocular ompA variants A, B, Ba and C are typically found within the phylogenetically coherent "classical ocular lineage". However, variants B, Ba and C have also been found within three distinct strains in Australia, all associated with ocular disease in children and outside the classical ocular lineage. CtGEM genotyping is a method for detecting and discriminating ocular strains and also the major phylogenetic lineages. The rationale was facilitation of surveillance to inform responses to C. trachomatis detection in UGT specimens from young children. CtGEM typing is based on high resolution melting analysis (HRMA) of two PCR amplified fragments with high combinatorial resolving power, as defined by computerised comparison of 65 whole genomes. One fragment is from the hypothetical gene defined by Jali-1891 in the C. trachomatis B_Jali20 genome, while the other is from ompA. Twenty combinatorial CtGEM types have been shown to exist, and these encompass unique genotypes for all known ocular strains, and also delineate the TI and T2 major phylogenetic lineages, identify LGV strains and provide additional resolution beyond this. CtGEM typing and Sanger sequencing were compared with 42 C. trachomatis positive clinical specimens, and there were no disjunctions. CtGEM typing is a highly efficient method designed and tested using large scale comparative genomics. It divides C. trachomatis into clinically and biologically meaningful groups, and may have broad application in surveillance.
沙眼衣原体感染泌尿生殖道(UGT)和眼睛。解剖学趋向性与主要外膜蛋白 ompA 编码的变异有关。具有眼部 ompA 变体 A、B、Ba 和 C 的菌株通常存在于系统发育一致的“经典眼部谱系”中。然而,变体 B、Ba 和 C 也在澳大利亚的三个不同菌株中发现,均与儿童眼部疾病有关,且不在经典眼部谱系内。CtGEM 基因分型是一种用于检测和区分眼部菌株以及主要进化谱系的方法。其基本原理是促进监测,以便对儿童 UGT 标本中沙眼衣原体的检测做出反应。CtGEM 分型基于两个 PCR 扩增片段的高分辨率熔解分析(HRMA),具有高组合分辨率,这是通过对 65 个全基因组的计算机比较来定义的。一个片段来自沙眼衣原体 B_Jali20 基因组中 Jali-1891 定义的假设基因,另一个片段来自 ompA。已经证明存在 20 种组合性 CtGEM 类型,这些类型包含所有已知眼部菌株的独特基因型,并且还划定了 TI 和 T2 主要进化谱系,鉴定了 LGV 菌株,并提供了超越此范围的额外分辨率。CtGEM 分型和 Sanger 测序与 42 个沙眼衣原体阳性临床标本进行了比较,没有分离。CtGEM 分型是一种高效的方法,使用大规模比较基因组学进行设计和测试。它将沙眼衣原体分为具有临床和生物学意义的组,并且可能在监测中具有广泛的应用。