Genomic Evidence for the Evolution of Streptococcus equi: Host Restriction, Increased Virulence, and Genetic Exchange with Human Pathogens

Matthew T. G. Holden(Wellcome Sanger Institute), Zoe Heather(Animal Health Trust), Romain Paillot(Animal Health Trust), Karen F. Steward(Animal Health Trust), K. Webb(Animal Health Trust), Fern Ainslie(Animal Health Trust), Thibaud Jourdan(Animal Health Trust), Nathalie Bason(Wellcome Sanger Institute), Nancy Holroyd(Wellcome Sanger Institute), Karen Mungall(Wellcome Sanger Institute), Michael A. Quail(Wellcome Sanger Institute), Mandy Sanders(Wellcome Sanger Institute), Mark Simmonds(Wellcome Sanger Institute), David L. Willey(Wellcome Sanger Institute), Karen Brooks(Wellcome Sanger Institute), David M. Aanensen(St Mary's Hospital), Brian G. Spratt(St Mary's Hospital), Keith A. Jolley(Medawar Building for Pathogen Research), Martin Maiden(Medawar Building for Pathogen Research), Michael Kehoe(Newcastle University), N. Chanter(Animal Health Trust), Stephen D. Bentley(Wellcome Sanger Institute), Carl Robinson(Animal Health Trust), Duncan J. Maskell(University of Cambridge), Julian Parkhill(Wellcome Sanger Institute), Andrew S. Waller(Animal Health Trust)
PLoS Pathogens
March 26, 2009
Cited by 263Open Access
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Abstract

The continued evolution of bacterial pathogens has major implications for both human and animal disease, but the exchange of genetic material between host-restricted pathogens is rarely considered. Streptococcus equi subspecies equi (S. equi) is a host-restricted pathogen of horses that has evolved from the zoonotic pathogen Streptococcus equi subspecies zooepidemicus (S. zooepidemicus). These pathogens share approximately 80% genome sequence identity with the important human pathogen Streptococcus pyogenes. We sequenced and compared the genomes of S. equi 4047 and S. zooepidemicus H70 and screened S. equi and S. zooepidemicus strains from around the world to uncover evidence of the genetic events that have shaped the evolution of the S. equi genome and led to its emergence as a host-restricted pathogen. Our analysis provides evidence of functional loss due to mutation and deletion, coupled with pathogenic specialization through the acquisition of bacteriophage encoding a phospholipase A(2) toxin, and four superantigens, and an integrative conjugative element carrying a novel iron acquisition system with similarity to the high pathogenicity island of Yersinia pestis. We also highlight that S. equi, S. zooepidemicus, and S. pyogenes share a common phage pool that enhances cross-species pathogen evolution. We conclude that the complex interplay of functional loss, pathogenic specialization, and genetic exchange between S. equi, S. zooepidemicus, and S. pyogenes continues to influence the evolution of these important streptococci.


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