Genome and Transcriptome Adaptation Accompanying Emergence of the Definitive Type 2 Host-Restricted <named-content content-type="genus-species">Salmonella enterica</named-content> Serovar Typhimurium Pathovar
Robert A. Kingsley,
Sally Kay,
Thomas Connor,
Lars Barquist,
Leanne Sait,
Kathryn E. Holt,
Karthi Sivaraman,
Thomas Wileman,
David Goulding,
Simon Clare,
Christine Hale,
Aswin Seshasayee,
Simon Harris,
Nicholas R. Thomson,
Paul Gardner,
Wolfgang Rabsch,
Paul Wigley,
Tom Humphrey,
Julian Parkhill,
Gordon Dougan
Affiliations
Robert A. Kingsley
The Wellcome Trust Sanger Institute, the Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom
Sally Kay
The Wellcome Trust Sanger Institute, the Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom
Thomas Connor
The Wellcome Trust Sanger Institute, the Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom
Lars Barquist
The Wellcome Trust Sanger Institute, the Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom
Leanne Sait
School of Veterinary Sciences, Langford, Bristol, United Kingdom
Kathryn E. Holt
The Wellcome Trust Sanger Institute, the Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom
Karthi Sivaraman
European Molecular Biology Laboratory Outstation-Hinxton, European Bioinformatics Institute, the Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom
Thomas Wileman
The Wellcome Trust Sanger Institute, the Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom
David Goulding
The Wellcome Trust Sanger Institute, the Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom
Simon Clare
Christine Hale
The Wellcome Trust Sanger Institute, the Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom
Aswin Seshasayee
European Molecular Biology Laboratory Outstation-Hinxton, European Bioinformatics Institute, the Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom
Simon Harris
The Wellcome Trust Sanger Institute, the Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom
Nicholas R. Thomson
The Wellcome Trust Sanger Institute, the Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom
Paul Gardner
The Wellcome Trust Sanger Institute, the Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom
Wolfgang Rabsch
National Reference Center for Salmonellae and other Enteric Pathogens, Robert Koch Institut, Wernigerode, Germany
Paul Wigley
Department of Infection Biology, University of Liverpool, Leahurst Campus, Liverpool, United Kingdom
Tom Humphrey
Department of Infection Biology, University of Liverpool, Leahurst Campus, Liverpool, United Kingdom
Julian Parkhill
The Wellcome Trust Sanger Institute, the Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom
Gordon Dougan
The Wellcome Trust Sanger Institute, the Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom
ABSTRACT Salmonella enterica serovar Typhimurium definitive type 2 (DT2) is host restricted to Columba livia (rock or feral pigeon) but is also closely related to S. Typhimurium isolates that circulate in livestock and cause a zoonosis characterized by gastroenteritis in humans. DT2 isolates formed a distinct phylogenetic cluster within S. Typhimurium based on whole-genome-sequence polymorphisms. Comparative genome analysis of DT2 94-213 and S. Typhimurium SL1344, DT104, and D23580 identified few differences in gene content with the exception of variations within prophages. However, DT2 94-213 harbored 22 pseudogenes that were intact in other closely related S. Typhimurium strains. We report a novel in silico approach to identify single amino acid substitutions in proteins that have a high probability of a functional impact. One polymorphism identified using this method, a single-residue deletion in the Tar protein, abrogated chemotaxis to aspartate in vitro. DT2 94-213 also exhibited an altered transcriptional profile in response to culture at 42°C compared to that of SL1344. Such differentially regulated genes included a number involved in flagellum biosynthesis and motility. IMPORTANCE Whereas Salmonella enterica serovar Typhimurium can infect a wide range of animal species, some variants within this serovar exhibit a more limited host range and altered disease potential. Phylogenetic analysis based on whole-genome sequences can identify lineages associated with specific virulence traits, including host adaptation. This study represents one of the first to link pathogen-specific genetic signatures, including coding capacity, genome degradation, and transcriptional responses to host adaptation within a Salmonella serovar. We performed comparative genome analysis of reference and pigeon-adapted definitive type 2 (DT2) S. Typhimurium isolates alongside phenotypic and transcriptome analyses, to identify genetic signatures linked to host adaptation within the DT2 lineage.