Insights into Genomic Variation within Salmonella enterica

Serrano Pc, P. Lam, Hern, ez Ye, Nava Gm
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Abstract

Advances in molecular microbiology, comparative genomics and data mining have allowed us to uncover new insights into genome structure within bacterial species. To evolve, Bacteria gains and loses genes and other genomic sequences to adapt to specific ecological niches [1]. Thus, the intraspecies genomic variation found in numerous bacterial species has highlighted the need of analyzing genome composition to define bacterial species [1]. Fortunately, Whole-Genome Sequence Analysis (WGSA) has uncovered the dynamic nature of genomic plasticity and the consequent extensive genetic diversity in Bacteria [2]. Currently, microbiological research has been focused on WGSA within-species to identify molecular or virulence determinants. These studies could accelerate our understanding of bacterial pathogenesis and strains-specific traits of virulence; key factors in improving bacterial surveillance and development of antibacterial treatments or vaccines [3]. Herein, we investigate the genomic variation within Salmonella enterica as an example of the potential of comparative analysis of WGSA to uncover intraspecies variation. A total of 1,604 S. enterica whole genomes were analyzed. This dataset comprised 38 different serotypes (Table 1) retrieved from the Integrated Microbial Genomes (IMG) system [4]. Serotypes with at least 3 genomes available were used for bioinformatics analyses. Intraspecies traits of genomic variation were assessed for each of the selected serotypes. Briefly, it was found that the genome size S. enterica serotypes varies considerably; for example, serotype Muenchen, in average, possess the largest genome size (5.00 Mbp) whereas Paratyphi possess the smallest (4.59 Mbp). Unexpectedly, a high variation in the genome size was observed in each serotype (Figure 1 and Table 1).
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肠道沙门氏菌基因组变异研究
分子微生物学、比较基因组学和数据挖掘的进步使我们能够发现细菌物种基因组结构的新见解。为了进化,细菌获得和失去基因和其他基因组序列,以适应特定的生态位[1]。因此,在许多细菌物种中发现的种内基因组变异突出了分析基因组组成来定义细菌物种的必要性[1]。幸运的是,全基因组序列分析(Whole-Genome Sequence Analysis, WGSA)揭示了细菌基因组可塑性的动态本质以及由此产生的广泛的遗传多样性[2]。目前,微生物学研究主要集中在物种内的WGSA,以确定分子或毒力决定因素。这些研究可以加速我们对细菌致病机制和菌株特异性毒力特征的理解;提高细菌监测和开发抗菌治疗或疫苗的关键因素[3]。在这里,我们研究肠道沙门氏菌的基因组变异,作为WGSA比较分析揭示种内变异的潜力的一个例子。共分析了1604份肠球菌全基因组。该数据集包括从集成微生物基因组(IMG)系统中检索的38种不同血清型(表1)[4]。至少有3个基因组可用的血清型用于生物信息学分析。对所选血清型的种内基因组变异特征进行了评估。简要地说,发现肠链球菌血清型的基因组大小差异很大;例如,平均而言,Muenchen血清型具有最大的基因组大小(5.00 Mbp),而副伤寒具有最小的基因组大小(4.59 Mbp)。出乎意料的是,在每种血清型中观察到基因组大小的高度变化(图1和表1)。
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