TY - JOUR
T1 - Sequencing and analysis of the genome of the Whipples disease bacterium Tropheryma whipplei
AU - Bentley, SD
AU - Maiwald, M
AU - Murphy, LD
AU - Pallen, Mark
AU - Yeats, CA
AU - Dover, Lynn
AU - Besra, Gurdyal
PY - 2003/2/22
Y1 - 2003/2/22
N2 - Background 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.
Methods We isolated and propagated T whipplei strain TWO8/27 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.
Findings Sequencing revealed a condensed 925 938 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.
Interpretation 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.
AB - Background 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.
Methods We isolated and propagated T whipplei strain TWO8/27 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.
Findings Sequencing revealed a condensed 925 938 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.
Interpretation 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.
UR - http://www.scopus.com/inward/record.url?scp=0037460735&partnerID=8YFLogxK
U2 - 10.1016/S0140-6736(03)12597-4
DO - 10.1016/S0140-6736(03)12597-4
M3 - Article
C2 - 12606174
SN - 1474-547X
VL - 361
SP - 637
EP - 644
JO - Lancet
JF - Lancet
IS - 9358
ER -