Seth-Smith Helena M B, Imkamp Frank, Tagini Florian, Cuénod Aline, Hömke Rico, Jahn Kathleen, Tschacher Anne, Grendelmeier Peter, Bättig Veronika, Erb Stefan, Reinhard Miriam, Rütimann Gottfried, Borrell Sonia, Gagneux Sebastien, Casanova Carlo, Droz Sara, Osthoff Michael, Tamm Michael, Nübel Ulrich, Greub Gilbert, Keller Peter M, Egli Adrian
Division of Clinical Microbiology, University Hospital Basel, Basel, Switzerland.
Applied Microbiology Research, Department of Biomedicine, University of Basel, Basel, Switzerland.
Front Microbiol. 2019 Jan 8;9:3184. doi: 10.3389/fmicb.2018.03184. eCollection 2018.
Bacteria belonging to the genus are predominantly responsible for pulmonary diseases; most notably causes granulomatous pulmonary infections. Here we describe a novel slow growing mycobacterial species isolated from respiratory samples from five patients, four with underlying pulmonary disease. The isolates were characterized by biochemical and molecular techniques, including whole genome sequencing. Biochemical characteristics generally match those of and ; however, the most striking difference of the new species is its ability to grow at 37°C. The new species was found to grow in human macrophages, but not amoebae, suggesting a pathogenic rather than an environmental lifestyle. Phylogenetic analysis reveals a deep-rooting relationship to and . A complete genome sequence was obtained through combining short and long-read sequencing, providing a genome of 5.6 Mb. The genome appears to be highly intact, syntenic with that of , with very few insertion sequences. A vast array of virulence factors includes 283 PE/PPE surface-associated proteins, making up 10% of the coding capacity, and 22 non-ribosomal peptide synthase clusters. A comparison of six clinical isolates from the five patients shows that they differ by up to two single nucleotide polymorphisms, suggesting a common source of infection. Our findings are in accordance with the recognition of a new taxonomic entity. We propose the name , as all isolates were found in patients from the Basel area of Switzerland.
属于该属的细菌主要导致肺部疾病;最显著的是 引起肉芽肿性肺部感染。在此,我们描述了一种从五名患者的呼吸道样本中分离出的新型缓慢生长的分枝杆菌物种,其中四名患者患有潜在肺部疾病。通过生化和分子技术对分离株进行了表征,包括全基因组测序。生化特征总体上与 和 的特征相符;然而,新物种最显著的差异在于其在37°C下生长的能力。发现新物种能在人类巨噬细胞中生长,但不能在变形虫中生长,这表明其具有致病性而非环境生存方式。系统发育分析揭示了与 和 的深层亲缘关系。通过结合短读长和长读长测序获得了完整的基因组序列,提供了一个5.6 Mb的基因组。该基因组似乎高度完整,与 的基因组具有共线性,插入序列很少。大量的毒力因子包括283种与PE/PPE表面相关的蛋白质,占编码能力的10%,以及22个非核糖体肽合成酶簇。对五名患者的六个临床分离株的比较表明,它们之间最多相差两个单核苷酸多态性,这表明存在共同的感染源。我们的发现与识别一个新的分类实体一致。我们提议将其命名为 ,因为所有分离株均来自瑞士巴塞尔地区的患者。