Animal Health and Veterinary Laboratories Agency, Woodham Lane, New Haw, Addlestone, Surrey, UK.
BMC Genomics. 2013 May 31;14:365. doi: 10.1186/1471-2164-14-365.
Despite the frequent isolation of Salmonella enterica sub. enterica serovars Derby and Mbandaka from livestock in the UK and USA little is known about the biological processes maintaining their prevalence. Statistics for Salmonella isolations from livestock production in the UK show that S. Derby is most commonly associated with pigs and turkeys and S. Mbandaka with cattle and chickens. Here we compare the first sequenced genomes of S. Derby and S. Mbandaka as a basis for further analysis of the potential host adaptations that contribute to their distinct host species distributions.
Comparative functional genomics using the RAST annotation system showed that predominantly mechanisms that relate to metabolite utilisation, in vivo and ex vivo persistence and pathogenesis distinguish S. Derby from S. Mbandaka. Alignment of the genome nucleotide sequences of S. Derby D1 and D2 and S. Mbandaka M1 and M2 with Salmonella pathogenicity islands (SPI) identified unique complements of genes associated with host adaptation. We also describe a new genomic island with a putative role in pathogenesis, SPI-23. SPI-23 is present in several S. enterica serovars, including S. Agona, S. Dublin and S. Gallinarum, it is absent in its entirety from S. Mbandaka.
We discovered a new 37 Kb genomic island, SPI-23, in the chromosome sequence of S. Derby, encoding 42 ORFS, ten of which are putative TTSS effector proteins. We infer from full-genome synonymous SNP analysis that these two serovars diverged, between 182kya and 625kya coinciding with the divergence of domestic pigs. The differences between the genomes of these serovars suggest they have been exposed to different stresses including, phage, transposons and prolonged externalisation. The two serovars possess distinct complements of metabolic genes; many of which cluster into pathways for catabolism of carbon sources.
尽管经常从英国和美国的牲畜中分离出肠炎沙门氏菌亚种。肠亚种血清型德比和曼巴达卡,但对维持其流行的生物学过程知之甚少。英国家畜生产中沙门氏菌分离株的统计数据显示,S. Derby 最常与猪和火鸡相关,而 S. Mbandaka 则与牛和鸡相关。在这里,我们比较了 S. Derby 和 S. Mbandaka 的第一个测序基因组,作为进一步分析有助于它们独特宿主分布的潜在宿主适应的基础。
使用 RAST 注释系统进行比较功能基因组学表明,主要与代谢物利用、体内和体外持久性以及发病机制相关的机制将 S. Derby 与 S. Mbandaka 区分开来。S. Derby D1 和 D2 与 S. Mbandaka M1 和 M2 的基因组核苷酸序列与沙门氏菌致病性岛(SPI)的比对确定了与宿主适应相关的独特基因组合。我们还描述了一个具有潜在发病机制作用的新基因组岛,SPI-23。SPI-23 存在于几个肠炎沙门氏菌血清型中,包括 S. Agona、S. Dublin 和 S. Gallinarum,而在其整个 Mbandaka 中均不存在。
我们在 S. Derby 染色体序列中发现了一个新的 37 Kb 基因组岛,SPI-23,编码 42 个 ORFS,其中 10 个是推定的 TTSS 效应蛋白。我们从全基因组同义 SNP 分析推断,这两个血清型在 182kya 和 625kya 之间发生分歧,与家猪的分化时间相吻合。这两个血清型基因组之间的差异表明它们已经暴露于不同的压力下,包括噬菌体、转座子和长时间的外化。这两个血清型具有不同的代谢基因组合;其中许多基因簇成碳源分解代谢途径。