Cardiff School of Biosciences, Cardiff, United Kingdom; Pathogen Genomics, Wellcome Trust Sanger Centre, Cambridge, United Kingdom
Clare R Barker
Cardiff School of Biosciences, Cardiff, United Kingdom
Kate S Baker
Pathogen Genomics, Wellcome Trust Sanger Centre, Cambridge, United Kingdom
François-Xavier Weill
Unité des Bactéries Pathogènes Entériques, Institut Pasteur, Paris, France
Kaisar Ali Talukder
Centre for Food and Water Borne Diseases, International Centre for Diarrhoeal Disease Research, Dhaka, Bangladesh
Anthony M Smith
Centre for Enteric Diseases, National Institute for Communicable Diseases and Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa
Stephen Baker
The Hospital for Tropical Diseases, Wellcome Trust Major Overseas Programme, Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam; Centre for Tropical Medicine, Nuffield Department of Clinical Medicine, Oxford University, Oxford, United Kingdom; The London School of Hygiene and Tropical Medicine, London, United Kingdom
Malika Gouali
Unité des Bactéries Pathogènes Entériques, Institut Pasteur, Paris, France
Duy Pham Thanh
The Hospital for Tropical Diseases, Wellcome Trust Major Overseas Programme, Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam; Centre for Tropical Medicine, Nuffield Department of Clinical Medicine, Oxford University, Oxford, United Kingdom; The London School of Hygiene and Tropical Medicine, London, United Kingdom
Ishrat Jahan Azmi
Centre for Food and Water Borne Diseases, International Centre for Diarrhoeal Disease Research, Dhaka, Bangladesh
Wanderley Dias da Silveira
Department of Genetics, Evolution, and Bioagents, Institute of Biology, University of Campinas, São Paulo, Brazil
Torsten Semmler
Centre for Infection Medicine, Institute of Microbiology and Epizootics, Freie University, Berlin, Germany; Robert Koch Institute, Berlin, Germany
Lothar H Wieler
Centre for Infection Medicine, Institute of Microbiology and Epizootics, Freie University, Berlin, Germany; Robert Koch Institute, Berlin, Germany
Claire Jenkins
Gastrointestinal Bacteria Reference Unit, Public Health England, London, United Kingdom
Alejandro Cravioto
Global Evaluative Sciences, Inc., Seattle, United States
Shah M Faruque
Centre for Food and Water Borne Diseases, International Centre for Diarrhoeal Disease Research, Dhaka, Bangladesh
Julian Parkhill
Pathogen Genomics, Wellcome Trust Sanger Centre, Cambridge, United Kingdom
Dong Wook Kim
Department of Pharmacy, School of Pharmacy, Hanyang University, Ansan, Republic of Korea
Karen H Keddy
Centre for Enteric Diseases, National Institute for Communicable Diseases and Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa
Nicholas R Thomson
Pathogen Genomics, Wellcome Trust Sanger Centre, Cambridge, United Kingdom; The London School of Hygiene and Tropical Medicine, London, United Kingdom
Shigella flexneri is the most common cause of bacterial dysentery in low-income countries. Despite this, S. flexneri remains largely unexplored from a genomic standpoint and is still described using a vocabulary based on serotyping reactions developed over half-a-century ago. Here we combine whole genome sequencing with geographical and temporal data to examine the natural history of the species. Our analysis subdivides S. flexneri into seven phylogenetic groups (PGs); each containing two-or-more serotypes and characterised by distinct virulence gene complement and geographic range. Within the S. flexneri PGs we identify geographically restricted sub-lineages that appear to have persistently colonised regions for many decades to over 100 years. Although we found abundant evidence of antimicrobial resistance (AMR) determinant acquisition, our dataset shows no evidence of subsequent intercontinental spread of antimicrobial resistant strains. The pattern of colonisation and AMR gene acquisition suggest that S. flexneri has a distinct life-cycle involving local persistence.