Whole-genome sequences of Chlamydia trachomatis directly from clinical samples without culture.


Seth-Smith, HM; Harris, SR; Skilton, RJ; Radebe, FM; Golparian, D; Shipitsyna, E; Duy, PT; Scott, P; Cutcliffe, LT; O'Neill, C; Parmar, S; Pitt, R; Baker, S; Ison, CA; Marsh, P; Jalal, H; Lewis, DA; Unemo, M; Clarke, IN; Parkhill, J; Thomson, NR; (2013) Whole-genome sequences of Chlamydia trachomatis directly from clinical samples without culture. Genome research, 23 (5). pp. 855-66. ISSN 1088-9051 DOI: https://doi.org/10.1101/gr.150037.112

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Abstract

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 human DNA. To determine whether it is possible to obtain whole-genome sequences from bacteria without the need for culture, we have devised an approach that combines immunomagnetic separation (IMS) for targeted bacterial enrichment with multiple displacement amplification (MDA) for whole-genome amplification. Using IMS-MDA in conjunction with high-throughput multiplexed Illumina sequencing, we have produced the first whole bacterial genome sequences direct from clinical samples. We also show that this method can be used to generate genome data from nonviable archived samples. This method will prove a useful tool in answering questions relating to the biology of many difficult-to-culture or fastidious bacteria of clinical concern.

Item Type: Article
Faculty and Department: Faculty of Infectious and Tropical Diseases > Dept of Pathogen Molecular Biology
PubMed ID: 23525359
Web of Science ID: 318202400010
URI: http://researchonline.lshtm.ac.uk/id/eprint/1229394

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