Buultjens Andrew H, Lam Margaret M C, Ballard Susan, Monk Ian R, Mahony Andrew A, Grabsch Elizabeth A, Grayson M Lindsay, Pang Stanley, Coombs Geoffrey W, Robinson J Owen, Seemann Torsten, Johnson Paul D R, Howden Benjamin P, Stinear Timothy P
Department of Microbiology and Immunology, Doherty Institute for Infection and Immunity, University of Melbourne , Melbourne , Victoria , Australia.
Microbiology Diagnostic Unit, Department of Microbiology and Immunology, Doherty Institute for Infection and Immunity, University of Melbourne , Melbourne , Victoria , Australia.
PeerJ. 2017 Jan 24;5:e2916. doi: 10.7717/peerj.2916. eCollection 2017.
From early 2012, a novel clone of vancomycin resistant (assigned the multi locus sequence type ST796) was simultaneously isolated from geographically separate hospitals in south eastern Australia and New Zealand. Here we describe the complete genome sequence of Ef_aus0233, a representative ST796 isolate. We used PacBio single molecule real-time sequencing to establish a high quality, fully assembled genome comprising a circular chromosome of 2,888,087 bp and five plasmids. Comparison of Ef_aus0233 to other genomes shows Ef_aus0233 is a member of the epidemic hospital-adapted lineage and has evolved from an ST555-like ancestral progenitor by the accumulation or modification of five mosaic plasmids and five putative prophage, acquisition of two cryptic genomic islands, accrued chromosomal single nucleotide polymorphisms and a 80 kb region of recombination, also gaining Tn and Tn, transposons conferring resistance to vancomycin and tetracycline respectively. The genomic dissection of this new clone presented here underscores the propensity of the hospital lineage to change, presumably in response to the specific conditions of hospital and healthcare environments.
从2012年初开始,一种新型耐万古霉素克隆株(被指定为多位点序列类型ST796)同时从澳大利亚东南部和新西兰地理位置分散的医院中分离出来。在此,我们描述了Ef_aus0233(一种代表性的ST796分离株)的完整基因组序列。我们使用PacBio单分子实时测序技术构建了一个高质量、完全组装的基因组,该基因组由一条2,888,087 bp的环状染色体和五个质粒组成。将Ef_aus0233与其他基因组进行比较发现,Ef_aus0233是流行的医院适应谱系的成员,它由一个类似ST555的祖先通过五个嵌合质粒和五个推定前噬菌体的积累或修饰、两个隐秘基因组岛的获得、累积的染色体单核苷酸多态性以及一个80 kb的重组区域进化而来,还获得了Tn和Tn转座子,分别赋予对万古霉素和四环素的抗性。此处展示的对这个新克隆株的基因组剖析强调了医院谱系发生变化的倾向,推测是对医院和医疗环境的特定条件作出的反应。