Variant Surface Glycoprotein gene repertoires in <it>Trypanosoma brucei </it>have diverged to become strain-specific

<p>Abstract</p> <p>Background</p> <p>In a mammalian host, the cell surface of African trypanosomes is protected by a monolayer of a single variant surface glycoprotein (VSG). The VSG is central to antigenic variation; one VSG gene is expressed at any one time and there...

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Main Authors: Sharma Reuben, Mott Helen, Jones Nicola G, Picozzi Kim, Hutchinson O Clyde, Welburn Susan C, Carrington Mark
Format: Article
Language:English
Published: BMC 2007-07-01
Series:BMC Genomics
Online Access:http://www.biomedcentral.com/1471-2164/8/234
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spelling doaj-40c1b0908925406388054f0481215c2f2020-11-25T01:03:49ZengBMCBMC Genomics1471-21642007-07-018123410.1186/1471-2164-8-234Variant Surface Glycoprotein gene repertoires in <it>Trypanosoma brucei </it>have diverged to become strain-specificSharma ReubenMott HelenJones Nicola GPicozzi KimHutchinson O ClydeWelburn Susan CCarrington Mark<p>Abstract</p> <p>Background</p> <p>In a mammalian host, the cell surface of African trypanosomes is protected by a monolayer of a single variant surface glycoprotein (VSG). The VSG is central to antigenic variation; one VSG gene is expressed at any one time and there is a low frequency stochastic switch to expression of a different VSG gene. The genome of <it>Trypanosoma brucei </it>contains a repertoire of > 1000 VSG sequences. The degree of conservation of the genomic VSG repertoire in different strains has not been investigated in detail.</p> <p>Results</p> <p>Eighteen expressed VSGs from Ugandan isolates were compared with homologues (> 40 % sequence identity) in the two available <it>T. brucei </it>genome sequences. Fourteen homologues were present in the genome of <it>Trypanosoma brucei brucei </it>TREU927 from Kenya and fourteen in the genome of <it>T. b. gambiense </it>Dal972 from Cote d'Ivoire. The Ugandan VSGs averaged 71% and 73 % identity to homologues in <it>T. b. brucei </it>and <it>T. b. gambiense </it>respectively. The sequence divergence between homologous VSGs from the three different strains was not random but was more prevalent in the parts of the VSG believed to interact with the host immune system on the living trypanosome.</p> <p>Conclusion</p> <p>It is probable that the VSG repertoires in the different isolates contain many common VSG genes. The location of divergence between VSGs is consistent with selection for strain-specific VSG repertoires, possibly to allow superinfection of an animal by a second strain. A consequence of strain-specific VSG repertoires is that any vaccine based on large numbers of VSGs from a single strain will only provide partial protection against other strains.</p> http://www.biomedcentral.com/1471-2164/8/234
collection DOAJ
language English
format Article
sources DOAJ
author Sharma Reuben
Mott Helen
Jones Nicola G
Picozzi Kim
Hutchinson O Clyde
Welburn Susan C
Carrington Mark
spellingShingle Sharma Reuben
Mott Helen
Jones Nicola G
Picozzi Kim
Hutchinson O Clyde
Welburn Susan C
Carrington Mark
Variant Surface Glycoprotein gene repertoires in <it>Trypanosoma brucei </it>have diverged to become strain-specific
BMC Genomics
author_facet Sharma Reuben
Mott Helen
Jones Nicola G
Picozzi Kim
Hutchinson O Clyde
Welburn Susan C
Carrington Mark
author_sort Sharma Reuben
title Variant Surface Glycoprotein gene repertoires in <it>Trypanosoma brucei </it>have diverged to become strain-specific
title_short Variant Surface Glycoprotein gene repertoires in <it>Trypanosoma brucei </it>have diverged to become strain-specific
title_full Variant Surface Glycoprotein gene repertoires in <it>Trypanosoma brucei </it>have diverged to become strain-specific
title_fullStr Variant Surface Glycoprotein gene repertoires in <it>Trypanosoma brucei </it>have diverged to become strain-specific
title_full_unstemmed Variant Surface Glycoprotein gene repertoires in <it>Trypanosoma brucei </it>have diverged to become strain-specific
title_sort variant surface glycoprotein gene repertoires in <it>trypanosoma brucei </it>have diverged to become strain-specific
publisher BMC
series BMC Genomics
issn 1471-2164
publishDate 2007-07-01
description <p>Abstract</p> <p>Background</p> <p>In a mammalian host, the cell surface of African trypanosomes is protected by a monolayer of a single variant surface glycoprotein (VSG). The VSG is central to antigenic variation; one VSG gene is expressed at any one time and there is a low frequency stochastic switch to expression of a different VSG gene. The genome of <it>Trypanosoma brucei </it>contains a repertoire of > 1000 VSG sequences. The degree of conservation of the genomic VSG repertoire in different strains has not been investigated in detail.</p> <p>Results</p> <p>Eighteen expressed VSGs from Ugandan isolates were compared with homologues (> 40 % sequence identity) in the two available <it>T. brucei </it>genome sequences. Fourteen homologues were present in the genome of <it>Trypanosoma brucei brucei </it>TREU927 from Kenya and fourteen in the genome of <it>T. b. gambiense </it>Dal972 from Cote d'Ivoire. The Ugandan VSGs averaged 71% and 73 % identity to homologues in <it>T. b. brucei </it>and <it>T. b. gambiense </it>respectively. The sequence divergence between homologous VSGs from the three different strains was not random but was more prevalent in the parts of the VSG believed to interact with the host immune system on the living trypanosome.</p> <p>Conclusion</p> <p>It is probable that the VSG repertoires in the different isolates contain many common VSG genes. The location of divergence between VSGs is consistent with selection for strain-specific VSG repertoires, possibly to allow superinfection of an animal by a second strain. A consequence of strain-specific VSG repertoires is that any vaccine based on large numbers of VSGs from a single strain will only provide partial protection against other strains.</p>
url http://www.biomedcentral.com/1471-2164/8/234
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