TY - JOUR
T1 - Comprehensive global genome dynamics of Chlamydia trachomatis show ancient diversification followed by contemporary mixing and recent lineage expansion
AU - Hadfield, James
AU - Harris, Simon R.
AU - Seth-Smith, Helena M.B.
AU - Parmar, Surendra
AU - Andersson, Patiyan
AU - Giffard, Philip M.
AU - Schachter, Julius
AU - Moncada, Jeanne
AU - Ellison, Louise
AU - Vaulet, María Lucía Gallo
AU - Fermepin, Marcelo Rodríguez
AU - Radebe, Frans
AU - Mendoza, Suyapa
AU - Ouburg, Sander
AU - Morré, Servaas A.
AU - Sachse, Konrad
AU - Puolakkainen, Mirja
AU - Korhonen, Suvi J.
AU - Sonnex, Chris
AU - Wiggins, Rebecca
AU - Jalal, Hamid
AU - Brunelli, Tamara
AU - Casprini, Patrizia
AU - Pitt, Rachel
AU - Ison, Catherine
AU - Savicheva, Alevtina
AU - Shipitsyna, Elena
AU - Hadad, Ronza
AU - Kari, Laszlo
AU - Burton, Matthew J.
AU - Mabey, David
AU - Solomon, Anthony W.
AU - Lewis, David
AU - Marsh, Peter
AU - Unemo, Magnus
AU - Clarke, Ian N.
AU - Parkhill, Julian
AU - Thomson, Nicholas R.
N1 - Publisher Copyright:
© 2017 Hadfield et al.
PY - 2017/7
Y1 - 2017/7
N2 - 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.
AB - 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.
UR - https://www.scopus.com/pages/publications/85023741110
U2 - 10.1101/gr.212647.116
DO - 10.1101/gr.212647.116
M3 - Article
C2 - 28588068
AN - SCOPUS:85023741110
SN - 1088-9051
VL - 27
SP - 1220
EP - 1229
JO - Genome Research
JF - Genome Research
IS - 7
ER -