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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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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