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

Whole-genome sequences of Chlamydia trachomatis directly from clinical samples without culture
Whole-genome sequences of Chlamydia trachomatis directly from clinical samples without culture
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.
1088-9051
Seth-Smith, Helena M.B.
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Harris, Simon R.
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Skilton, Rachel J.
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Radebe, Frans M.
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Golparian, Daniel
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Shipitsyna, Elena
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Duy, Pham Thanh
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Scott, Paul
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Cutcliffe, Lesley T.
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O'Neill, Colette
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Parmar, Surendra
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Pitt, Rachel
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Baker, Stephen
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Ison, Catherine A.
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Marsh, Peter
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Jalal, Hamid
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Lewis, David A.
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Unemo, Magnus
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Clarke, Ian N.
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Parkhill, Julian
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Thomson, Nicholas R.
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Seth-Smith, Helena M.B.
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Harris, Simon R.
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Skilton, Rachel J.
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Radebe, Frans M.
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Golparian, Daniel
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Shipitsyna, Elena
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Duy, Pham Thanh
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Scott, Paul
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Cutcliffe, Lesley T.
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O'Neill, Colette
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Parmar, Surendra
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Pitt, Rachel
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Baker, Stephen
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Ison, Catherine A.
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Marsh, Peter
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Jalal, Hamid
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Lewis, David A.
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Unemo, Magnus
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Clarke, Ian N.
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Parkhill, Julian
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Thomson, Nicholas R.
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Seth-Smith, Helena M.B., Harris, Simon R., Skilton, Rachel J., Radebe, Frans M., Golparian, Daniel, Shipitsyna, Elena, Duy, Pham Thanh, Scott, Paul, Cutcliffe, Lesley T., O'Neill, Colette, Parmar, Surendra, Pitt, Rachel, Baker, Stephen, Ison, Catherine A., Marsh, Peter, Jalal, Hamid, Lewis, David A., Unemo, Magnus, Clarke, Ian N., Parkhill, Julian and Thomson, Nicholas R. (2013) Whole-genome sequences of Chlamydia trachomatis directly from clinical samples without culture. Genome Research. (doi:10.1101/gr.150037.112). (PMID:23525359)

Record type: Article

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.

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More information

e-pub ahead of print date: 22 March 2013
Organisations: Clinical & Experimental Sciences

Identifiers

Local EPrints ID: 350916
URI: http://eprints.soton.ac.uk/id/eprint/350916
ISSN: 1088-9051
PURE UUID: 9fc8ae1a-85bf-4f9d-9ce0-cf7fffe437a4
ORCID for Ian N. Clarke: ORCID iD orcid.org/0000-0002-4938-1620

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Date deposited: 11 Apr 2013 08:46
Last modified: 15 Mar 2024 02:33

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Contributors

Author: Helena M.B. Seth-Smith
Author: Simon R. Harris
Author: Rachel J. Skilton
Author: Frans M. Radebe
Author: Daniel Golparian
Author: Elena Shipitsyna
Author: Pham Thanh Duy
Author: Paul Scott
Author: Lesley T. Cutcliffe
Author: Colette O'Neill
Author: Surendra Parmar
Author: Rachel Pitt
Author: Stephen Baker
Author: Catherine A. Ison
Author: Peter Marsh
Author: Hamid Jalal
Author: David A. Lewis
Author: Magnus Unemo
Author: Ian N. Clarke ORCID iD
Author: Julian Parkhill
Author: Nicholas R. Thomson

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