1Division of Infection and Immunity, The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Easter Bush EH25 9RG, UK.
2Gastrointestinal Bacterial Reference Unit, 61 Colindale Avenue, Public Health England, London NW9 5EQ, UK.
Microb Genom. 2016 Dec 12;2(12):e000096. doi: 10.1099/mgen.0.000096. eCollection 2016 Dec.
Enterohaemorrhagic (EHEC) O157 is a zoonotic pathogen for which colonization of cattle and virulence in humans is associated with multiple horizontally acquired genes, the majority present in active or cryptic prophages. Our understanding of the evolution and phylogeny of EHEC O157 continues to develop primarily based on core genome analyses; however, such short-read sequences have limited value for the analysis of prophage content and its chromosomal location. In this study, we applied Single Molecule Real Time (SMRT) sequencing, using the Pacific Biosciences long-read sequencing platform, to isolates selected from the main sub-clusters of this clonal group. Prophage regions were extracted from these sequences and from published reference strains. Genome position and prophage diversity were analysed along with genetic content. Prophages could be assigned to clusters, with smaller prophages generally exhibiting less diversity and preferential loss of structural genes. Prophages encoding Shiga toxin (Stx) 2a and Stx1a were the most diverse, and more variable compared to prophages encoding Stx2c, further supporting the hypothesis that Stx2c-prophage integration was ancestral to acquisition of other Stx types. The concept that phage type (PT) 21/28 (Stx2a+, Stx2c+) strains evolved from PT32 (Stx2c+) was supported by analysis of strains with excised Stx-encoding prophages. Insertion sequence elements were over-represented in prophage sequences compared to the rest of the genome, showing integration in key genes such as and an excisionase, the latter potentially acting to capture the bacteriophage into the genome. Prophage profiling should allow more accurate prediction of the pathogenic potential of isolates.
肠出血性大肠杆菌(EHEC)O157 是一种人畜共患病原体,其在牛中的定植和对人类的毒力与多种水平获得的基因有关,这些基因主要存在于活跃或隐蔽的原噬菌体中。我们对 EHEC O157 的进化和系统发育的理解主要基于核心基因组分析;然而,这种短读序列对于原噬菌体内容及其染色体位置的分析价值有限。在这项研究中,我们应用单分子实时(SMRT)测序,使用 Pacific Biosciences 长读测序平台,对该克隆群的主要亚群中选择的分离株进行测序。从这些序列和已发表的参考菌株中提取原噬菌体区域。分析了基因组位置和原噬菌体多样性以及遗传内容。可以将原噬菌体分配到聚类中,较小的原噬菌体通常表现出较低的多样性和结构基因的优先缺失。编码志贺毒素(Stx)2a 和 Stx1a 的原噬菌体是最多样化的,与编码 Stx2c 的原噬菌体相比,更具变异性,这进一步支持了 Stx2c-原噬菌体整合是获得其他 Stx 类型的祖先的假说。通过分析带有切除 Stx 编码原噬菌体的菌株,支持了 PT21/28(Stx2a+,Stx2c+)菌株从 PT32(Stx2c+)进化而来的概念。与基因组的其余部分相比,插入序列元件在原噬菌体序列中过度表达,表明其在关键基因如 和一个切除酶中整合,后者可能将噬菌体捕获到基因组中。原噬菌体分析应该能够更准确地预测分离株的致病潜力。