Abstract

Salmonella enterica subsp. enterica bacteria are highly diverse foodborne pathogens that are subdivided into more than 1,500 serovars. The diversity is believed to result from mutational evolution, as well as intra- and interspecies recombination that potentially could be influenced by restriction-modification (RM) systems. The aim of this study was to investigate whether RM systems were linked to the evolution of Salmonella enterica subsp. enterica. The study included 221 Salmonella enterica genomes, of which 68 were de novo sequenced and 153 were public available genomes from ENA. The data set covered 97 different serovars of Salmonella enterica subsp. enterica and an additional five genomes from four other Salmonella subspecies as an outgroup for constructing the phylogenetic trees. The phylogenetic trees were constructed based on multiple alignment of core genes, as well as the presence or absence of pangenes. The topology of the trees was compared to the presence of RM systems, antimicrobial resistance (AMR) genes, Salmonella pathogenicity islands (SPIs), and plasmid replicons. We did not observe any correlation between evolution and the RM systems in S.enterica subsp. enterica. However, sublineage correlations and serovar-specific patterns were observed. Additionally, we conclude that plasmid replicons, SPIs, and AMR were all better correlated to serovars than to RM systems. This study suggests a limited influence of RM systems on the evolution of Salmonella enterica subsp. enterica, which could be due to the conjugational mode of horizontal gene transfer in Salmonella. Thus, we conclude that other factors must be involved in shaping the evolution of bacteria. IMPORTANCE The evolution of bacterial pathogens, their plasticity and ability to rapidly change and adapt to new surroundings are crucial for understanding the epidemiology and public health. With the application of genomics, it became clear that horizontal gene transfer played a key role in evolution. To understand the evolution and diversification of pathogens, we need to understand the processes that drive the horizontal gene transfer. Restriction-modification systems are thought to cause rearrangements within the chromosome, as well as act as a barrier to horizontal gene transfer. However, here we show that the correlation between restriction-modification systems and evolution in other bacterial species does not apply to Salmonella enterica subsp. enterica. In summary, from this work, we conclude that other mechanisms might be involved in controlling and shaping the evolution of Salmonella enterica subsp. enterica.

Highlights

  • Salmonella enterica subsp. enterica bacteria are highly diverse foodborne pathogens that are subdivided into more than 1,500 serovars

  • For decades, RM systems have been recognized for their ability to act as “immune systems” for bacteria, helping to determine whether or not foreign DNA was established in the cell

  • For N. meningitidis, the impact of RM systems in evolution was recently elucidated, and the purpose of the current study was to clarify whether a similar association could be identified in S. enterica subsp. enterica, by investigating a large subset of different whole-genome-sequenced S. enterica subsp. enterica serovars and an outgroup of five genomes from other subspecies

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Summary

Introduction

Salmonella enterica subsp. enterica bacteria are highly diverse foodborne pathogens that are subdivided into more than 1,500 serovars. This study suggests a limited influence of RM systems on the evolution of Salmonella enterica subsp. Restriction-modification systems are thought to cause rearrangements within the chromosome, as well as act as a barrier to horizontal gene transfer. Here we show that the correlation between restrictionmodification systems and evolution in other bacterial species does not apply to Salmonella enterica subsp. Rearrangements of genomes caused by RM systems are described as factors that could influence the evolution of pathogens [4] In addition to their role in rearrangements, RM systems are considered to be a barrier for horizontal gene transfer (HGT) between bacteria, serving as an immune defense system for uptake of foreign DNA [8,9,10]. This enables the bacterium to distinguish between its own (methylated) DNA and incoming nonmethylated DNA

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