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PMID: 12606174 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Sequencing and analysis of the genome of the Whipple's disease bacterium Tropheryma whipplei.

Lancet (London, England) ·Vol. 361 ·No. 9358 ·2003-02-22 ·Pages 637-44

Bentley SD, Maiwald M, Murphy LD, Pallen MJ, Yeats CA, Dover LG, Norbertczak HT, Besra GS, Quail MA, Harris DE, von Herbay A, Goble A, Rutter S, Squares R, Squares S, Barrell BG, Parkhill J, Relman DA

Abstract

Whipple's disease is a rare multisystem chronic infection, involving the intestinal tract as well as various other organs. The causative agent, Tropheryma whipplei, is a Gram-positive bacterium about which little is known. Our aim was to investigate the biology of this organism by generating and analysing the complete DNA sequence of its genome. We isolated and propagated T whipplei strain TW08/27 from the cerebrospinal fluid of a patient diagnosed with Whipple's disease. We generated the complete sequence of the genome by the whole genome shotgun method, and analysed it with a combination of automatic and manual bioinformatic techniques. Sequencing revealed a condensed 925938 bp genome with a lack of key biosynthetic pathways and a reduced capacity for energy metabolism. A family of large surface proteins was identified, some associated with large amounts of non-coding repetitive DNA, and an unexpected degree of sequence variation. The genome reduction and lack of metabolic capabilities point to a host-restricted lifestyle for the organism. The sequence variation indicates both known and novel mechanisms for the elaboration and variation of surface structures, and suggests that immune evasion and host interaction play an important part in the lifestyle of this persistent bacterial pathogen.

MeSH Terms
Female Genome Gram-Positive Bacteria/genetics,isolation & purification,pathogenicity Humans Sequence Analysis, DNA Whipple Disease/genetics,microbiology
Authors & Affiliations
18 authors, click to expand affiliations / ORCID
Bentley Stephen D
The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, UK.
Maiwald Matthias
Murphy Lee D
Pallen Mark J
Yeats Corin A
Dover Lynn G
Norbertczak Halina T
Besra Gurdyal S
Quail Michael A
Harris David E
von Herbay Axel
Goble Arlette
Rutter Simon
Squares Robert
Squares Stephen
Barrell Bart G
Parkhill Julian
Relman David A
Article Info
Journal
Lancet (London, England)
Abbr.
Lancet
ISSN
0140-6736
Published
2003-02-22
Pages
637-44
Language
English
Region
England
NLM ID
2985213R
Subset
IM
Grants
NIDDK NIH HHS · DK56339 · United States
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