作者
Helena MB Seth-Smith, Simon R Harris, Rachel J Skilton, Frans M Radebe, Daniel Golparian, Elena Shipitsyna, Pham Thanh Duy, Paul Scott, Lesley T Cutcliffe, Colette O’Neill, Surendra Parmar, Rachel Pitt, Stephen Baker, Catherine A Ison, Peter Marsh, Hamid Jalal, David A Lewis, Magnus Unemo, Ian N Clarke, Julian Parkhill, Nicholas R Thomson
发表日期
2013/5/1
期刊
Genome research
卷号
23
期号
5
页码范围
855-866
出版商
Cold Spring Harbor Lab
简介
The use of whole-genome sequencing as a tool for the study of infectious bacteria is of growing clinical interest. Chlamydia trachomatis is responsible for sexually transmitted infections and the blinding disease trachoma, which affect hundreds of millions of people worldwide. Recombination is widespread within the genome of C. trachomatis, thus whole-genome sequencing is necessary to understand the evolution, diversity, and epidemiology of this pathogen. Culture of C. trachomatis has, until now, been a prerequisite to obtain DNA for whole-genome sequencing; however, as C. trachomatis is an obligate intracellular pathogen, this procedure is technically demanding and time consuming. Discarded clinical samples represent a large resource for sequencing the genomes of pathogens, yet clinical swabs frequently contain very low levels of C. trachomatis DNA and large amounts of contaminating microbial and …
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