Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, UK.
Research Institute for Medicines (iMed.ULisboa), Faculdade de Farmácia, Universidade de Lisboa, Lisboa, Portugal.
Sci Rep. 2021 Mar 22;11(1):6491. doi: 10.1038/s41598-021-85724-2.
Klebsiella pneumoniae is an important nosocomial infectious agent with a high antimicrobial resistance (AMR) burden. The application of long read sequencing technologies is providing insights into bacterial chromosomal and putative extra-chromosomal genetic elements (PEGEs) associated with AMR, but also epigenetic DNA methylation, which is thought to play a role in cleavage of foreign DNA and expression regulation. Here, we apply the PacBio sequencing platform to eight Portuguese hospital isolates, including one carbapenemase producing isolate, to identify methylation motifs. The resulting assembled chromosomes were between 5.2 and 5.5Mbp in length, and twenty-six PEGEs were found. Four of our eight samples carry bla, a dominant Extended Spectrum Beta Lactamase in Europe. We identified methylation motifs that control Restriction-Modification systems, including GATC of the DNA adenine methylase (Dam), which methylates N6-methyladenine (m6A) across all our K. pneumoniae assemblies. There was a consistent lack of methylation by Dam of the GATC motif downstream of two genes: fosA, a locus associated with low level fosfomycin resistance, and tnpB transposase on IncFIB(K) plasmids. Overall, we have constructed eight high quality reference genomes of K. pneumoniae, with insights into horizontal gene transfer and methylation m6A motifs.
肺炎克雷伯菌是一种重要的医院感染病原体,具有很高的抗生素耐药性(AMR)负担。长读测序技术的应用为与 AMR 相关的细菌染色体和假定的染色体外遗传元件(PEGEs)提供了深入了解,还包括表观遗传 DNA 甲基化,它被认为在切割外源 DNA 和表达调控中发挥作用。在这里,我们应用 PacBio 测序平台对来自葡萄牙的 8 个医院分离株进行分析,包括一个产生碳青霉烯酶的分离株,以鉴定甲基化模体。得到的组装染色体长度在 5.2 到 5.5Mbp 之间,发现了 26 个 PEGEs。我们的 8 个样本中有 4 个携带 bla,这是欧洲一种主要的扩展谱β-内酰胺酶。我们鉴定了控制限制修饰系统的甲基化模体,包括 DNA 腺嘌呤甲基转移酶(Dam)的 GATC,它在我们所有的肺炎克雷伯菌组装体中甲基化 N6-甲基腺嘌呤(m6A)。有两个基因下游的 GATC motif 缺乏 Dam 甲基化:fosA,与低水平磷霉素抗性相关的基因座,以及 IncFIB(K) 质粒上的 tnpB 转座酶。总体而言,我们构建了 8 株高质量的肺炎克雷伯菌参考基因组,深入了解了水平基因转移和甲基化 m6A 模体。