Chander Atul M, Nair Ramesan G, Kaur Gurwinder, Kochhar Rakesh, Dhawan Devinder K, Bhadada Sanjay K, Mayilraj Shanmugam
Department of Biophysics, Panjab UniversityChandigarh, India; Department of Endocrinology, Postgraduate Institute of Medical Education and ResearchChandigarh, India.
Microbial Type Culture Collection and Gene bank, CSIR-Institute of Microbial Technology Chandigarh, India.
Front Microbiol. 2017 Feb 2;8:129. doi: 10.3389/fmicb.2017.00129. eCollection 2017.
Species of the genus have been isolated from different ecological niches, especially from saline habitats and reported as weak human pathogens causing asymptomatic bacteraemia. Here, for the first time we are reporting the genome sequence and pathogenomic analysis of a strain designated as CD08_7 isolated from the duodenal mucosa of a celiac disease patient, identified as . To date, only five strains of the genus ( strain NP1, sp. strain JCM 19054, sp. strain F and sp. strain AN1) have been whole genome sequenced and annotated. In the present study we have mapped and compared the virulence profile of strain CD08_7 along with other reference genomes which showed some characteristic features that could contribute to pathogenicity. The RAST (Rapid Annotation using Subsystem Technology) based genome mining revealed more genes responsible for pathogenicity in strain CD08_7 when compared with the other four sequenced strains. The studied categories were resistance to antibiotic and toxic compounds, invasion and intracellular resistance, membrane transport, stress response, osmotic stress, oxidative stress, phages and prophages and iron acquisition. A total of 1431 protein-encoding genes were identified in the genome of strain CD08_7 among which 163 were predicted to contribute for pathogenicity. Out of 163 genes only 59 were common to other genome, which shows the higher levels of genetic richness in strain CD08_7 that may contribute to its functional versatility. This study provides a comprehensive analysis on genome of strain CD08_7 and possibly indicates its importance as a clinical pathogen.
该属的物种已从不同的生态位中分离出来,尤其是从盐生栖息地分离得到,并被报道为引起无症状菌血症的弱人类病原体。在此,我们首次报告了从一名乳糜泻患者十二指肠黏膜分离出的一株命名为CD08_7的菌株的基因组序列和病原组学分析,该菌株被鉴定为 。迄今为止,该属仅有五株菌株( 菌株NP1、 菌株JCM 19054、 菌株F和 菌株AN1)进行了全基因组测序和注释。在本研究中,我们绘制并比较了 菌株CD08_7与其他参考基因组的毒力谱,结果显示了一些可能有助于致病的特征。基于RAST(利用子系统技术进行快速注释)的基因组挖掘表明,与其他四株测序菌株相比,菌株CD08_7中有更多负责致病的基因。研究的类别包括对抗生素和有毒化合物的抗性、侵袭和细胞内抗性、膜转运、应激反应、渗透应激、氧化应激、噬菌体和原噬菌体以及铁的获取。在菌株CD08_7的基因组中总共鉴定出1431个蛋白质编码基因,其中163个被预测对致病性有贡献。在这163个基因中,只有59个与其他基因组共有,这表明菌株CD08_7具有更高水平的遗传丰富度,这可能有助于其功能的多样性。本研究对 菌株CD08_7的基因组进行了全面分析,并可能表明其作为临床病原体的重要性。