Phylogenetics and Differentiation of <em>Salmonella</em> Newport Lineages by Whole Genome Sequencing

<div><p><em>Salmonella</em> Newport has ranked in the top three <em>Salmonella</em> serotypes associated with foodborne outbreaks from 1995 to 2011 in the United States. In the current study, we selected 26 <em>S</em>. Newport strains isolated from diverse sources and geographic locations and then conducted 454 shotgun pyrosequencing procedures to obtain 16–24 × coverage of high quality draft genomes for each strain. Comparative genomic analysis of 28 <em>S</em>. Newport strains (including 2 reference genomes) and 15 outgroup genomes identified more than 140,000 informative SNPs. A resulting phylogenetic tree consisted of four sublineages and indicated that <em>S</em>. Newport had a clear geographic structure. Strains from Asia were divergent from those from the Americas. Our findings demonstrated that analysis using whole genome sequencing data resulted in a more accurate picture of phylogeny compared to that using single genes or small sets of genes. We selected loci around the <em>mutS</em> gene of <em>S</em>. Newport to differentiate distinct lineages, including those between <em>invH</em> and <em>mutS</em> genes at the 3′ end of <em>Salmonella</em> Pathogenicity Island 1 (SPI-1), <em>ste</em> fimbrial operon, and Clustered, Regularly Interspaced, Short Palindromic Repeats (CRISPR) associated-proteins (<em>cas</em>). These genes in the outgroup genomes held high similarity with either <em>S</em>. Newport Lineage II or III at the same loci. <em>S</em>. Newport Lineages II and III have different evolutionary histories in this region and our data demonstrated genetic flow and homologous recombination events around <em>mutS</em>. The findings suggested that <em>S</em>. Newport Lineages II and III diverged early in the serotype evolution and have evolved largely independently. Moreover, we identified genes that could delineate sublineages within the phylogenetic tree and that could be used as potential biomarkers for trace-back investigations during outbreaks. Thus, whole genome sequencing data enabled us to better understand the genetic background of pathogenicity and evolutionary history of <em>S</em>. Newport and also provided additional markers for epidemiological response.</p>