Abstract

BackgroundAeromonas salmonicida subsp. salmonicida is a ubiquitous psychrophilic waterborne bacterium and a fish pathogen. The numerous mobile elements, especially insertion sequences (IS), in its genome promote rearrangements that impact its phenotype. One of the main virulence factors of this bacterium, its type three secretion system (TTSS), is affected by these rearrangements. In Aeromonas salmonicida subsp. salmonicida most of the TTSS genes are encoded in a single locus on a large plasmid called pAsa5, and may be lost when the bacterium is cultivated at a higher temperature (25 °C), producing non-virulent mutants. In a previous study, pAsa5-rearranged strains that lacked the TTSS locus on pAsa5 were produced using parental strains, including 01-B526. Some of the generated deletions were explained by homologous recombination between ISs found on pAsa5, whereas the others remained unresolved. To investigate those rearrangements, short- and long-read high-throughput sequencing technologies were used on the A. salmonicida subsp. salmonicida 01-B526 whole genome.ResultsWhole genome sequencing of the 01-B526 strain revealed that its pAsa5 has an additional IS copy, an ISAS5, compared to the reference strain (A449) sequence, which allowed for a previously unknown rearrangement to occur. It also appeared that 01-B526 bears a second large plasmid, named pAsa9, which shares 40 kbp of highly similar sequences with pAsa5. Following these discoveries, previously unexplained deletions were elucidated by genotyping. Furthermore, in one of the derived strains a fusion of pAsa5 and pAsa9, involving the newly discovered ISAS5 copy, was observed.ConclusionThe loss of TTSS and hence virulence is explained by one consistent mechanism: IS-driven homologous recombination. The similarities between pAsa9 and pAsa5 also provide another example of genetic diversity driven by ISs.

Highlights

  • Aeromonas salmonicida subsp. salmonicida is a ubiquitous psychrophilic waterborne bacterium and a fish pathogen

  • Characterization of pAsa9 A new plasmid sequence was obtained from the 01-B526 strain by combining short and long reads in a hybrid de novo assembly

  • Our results showed that PacBio sequencing could provide crucial information for plasmid architecture studies by allowing for proper separation of long repeated regions

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Summary

Introduction

Aeromonas salmonicida subsp. salmonicida is a ubiquitous psychrophilic waterborne bacterium and a fish pathogen. Some of the generated deletions were explained by homologous recombination between ISs found on pAsa, whereas the others remained unresolved To investigate those rearrangements, short- and long-read high-throughput sequencing technologies were used on the A. salmonicida subsp. Alternative treatment options against this pathogen would be beneficial [8,9,10] but developing new treatments requires a better understanding of its underlying mechanisms, such as pathogenicity [4, 11] This ubiquitous waterborne bacterium shows evidence of lateral gene transfer. Different kinds of recombination have formed plasmid and genomic island variants with altered gene contents that result in phenotypic changes [5, 6, 15,16,17,18,19] This bacterium, beyond mediating gene transfer, could provide a new combination of those genes

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