Author:
Hadfield James,Harris Simon R.,Seth-Smith Helena M.B.,Parmar Surendra,Andersson Patiyan,Giffard Philip M.,Schachter Julius,Moncada Jeanne,Ellison Louise,Vaulet María Lucía Gallo,Fermepin Marcelo Rodríguez,Radebe Frans,Mendoza Suyapa,Ouburg Sander,Morré Servaas A.,Sachse Konrad,Puolakkainen Mirja,Korhonen Suvi J.,Sonnex Chris,Wiggins Rebecca,Jalal Hamid,Brunelli Tamara,Casprini Patrizia,Pitt Rachel,Ison Cathy,Savicheva Alevtina,Shipitsyna Elena,Hadad Ronza,Kari Laszlo,Burton Matthew J.,Mabey David,Solomon Anthony W.,Lewis David,Marsh Peter,Unemo Magnus,Clarke Ian N.,Parkhill Julian,Thomson Nicholas R.
Abstract
Chlamydia trachomatis is the world's most prevalent bacterial sexually transmitted infection and leading infectious cause of blindness, yet it is one of the least understood human pathogens, in part due to the difficulties of in vitro culturing and the lack of available tools for genetic manipulation. Genome sequencing has reinvigorated this field, shedding light on the contemporary history of this pathogen. Here, we analyze 563 full genomes, 455 of which are novel, to show that the history of the species comprises two phases, and conclude that the currently circulating lineages are the result of evolution in different genomic ecotypes. Temporal analysis indicates these lineages have recently expanded in the space of thousands of years, rather than the millions of years as previously thought, a finding that dramatically changes our understanding of this pathogen's history. Finally, at a time when almost every pathogen is becoming increasingly resistant to antimicrobials, we show that there is no evidence of circulating genomic resistance in C. trachomatis.
Publisher
Cold Spring Harbor Laboratory
Subject
Genetics(clinical),Genetics