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Genome analysis and comparative genomics of a Giardia intestinalis assemblage E isolate
BACKGROUND: Giardia intestinalis is a protozoan parasite that causes diarrhea in a wide range of mammalian species. To further understand the genetic diversity between the Giardia intestinalis species, we have performed genome sequencing and analysis of a wild-type Giardia intestinalis sample from t...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3091692/ https://www.ncbi.nlm.nih.gov/pubmed/20929575 http://dx.doi.org/10.1186/1471-2164-11-543 |
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author | Jerlström-Hultqvist, Jon Franzén, Oscar Ankarklev, Johan Xu, Feifei Nohýnková, Eva Andersson, Jan O Svärd, Staffan G Andersson, Björn |
author_facet | Jerlström-Hultqvist, Jon Franzén, Oscar Ankarklev, Johan Xu, Feifei Nohýnková, Eva Andersson, Jan O Svärd, Staffan G Andersson, Björn |
author_sort | Jerlström-Hultqvist, Jon |
collection | PubMed |
description | BACKGROUND: Giardia intestinalis is a protozoan parasite that causes diarrhea in a wide range of mammalian species. To further understand the genetic diversity between the Giardia intestinalis species, we have performed genome sequencing and analysis of a wild-type Giardia intestinalis sample from the assemblage E group, isolated from a pig. RESULTS: We identified 5012 protein coding genes, the majority of which are conserved compared to the previously sequenced genomes of the WB and GS strains in terms of microsynteny and sequence identity. Despite this, there is an unexpectedly large number of chromosomal rearrangements and several smaller structural changes that are present in all chromosomes. Novel members of the VSP, NEK Kinase and HCMP gene families were identified, which may reveal possible mechanisms for host specificity and new avenues for antigenic variation. We used comparative genomics of the three diverse Giardia intestinalis isolates P15, GS and WB to define a core proteome for this species complex and to identify lineage-specific genes. Extensive analyses of polymorphisms in the core proteome of Giardia revealed differential rates of divergence among cellular processes. CONCLUSIONS: Our results indicate that despite a well conserved core of genes there is significant genome variation between Giardia isolates, both in terms of gene content, gene polymorphisms, structural chromosomal variations and surface molecule repertoires. This study improves the annotation of the Giardia genomes and enables the identification of functionally important variation. |
format | Text |
id | pubmed-3091692 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30916922011-05-11 Genome analysis and comparative genomics of a Giardia intestinalis assemblage E isolate Jerlström-Hultqvist, Jon Franzén, Oscar Ankarklev, Johan Xu, Feifei Nohýnková, Eva Andersson, Jan O Svärd, Staffan G Andersson, Björn BMC Genomics Research Article BACKGROUND: Giardia intestinalis is a protozoan parasite that causes diarrhea in a wide range of mammalian species. To further understand the genetic diversity between the Giardia intestinalis species, we have performed genome sequencing and analysis of a wild-type Giardia intestinalis sample from the assemblage E group, isolated from a pig. RESULTS: We identified 5012 protein coding genes, the majority of which are conserved compared to the previously sequenced genomes of the WB and GS strains in terms of microsynteny and sequence identity. Despite this, there is an unexpectedly large number of chromosomal rearrangements and several smaller structural changes that are present in all chromosomes. Novel members of the VSP, NEK Kinase and HCMP gene families were identified, which may reveal possible mechanisms for host specificity and new avenues for antigenic variation. We used comparative genomics of the three diverse Giardia intestinalis isolates P15, GS and WB to define a core proteome for this species complex and to identify lineage-specific genes. Extensive analyses of polymorphisms in the core proteome of Giardia revealed differential rates of divergence among cellular processes. CONCLUSIONS: Our results indicate that despite a well conserved core of genes there is significant genome variation between Giardia isolates, both in terms of gene content, gene polymorphisms, structural chromosomal variations and surface molecule repertoires. This study improves the annotation of the Giardia genomes and enables the identification of functionally important variation. BioMed Central 2010-10-07 /pmc/articles/PMC3091692/ /pubmed/20929575 http://dx.doi.org/10.1186/1471-2164-11-543 Text en Copyright ©2010 Jerlström-Hultqvist et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Jerlström-Hultqvist, Jon Franzén, Oscar Ankarklev, Johan Xu, Feifei Nohýnková, Eva Andersson, Jan O Svärd, Staffan G Andersson, Björn Genome analysis and comparative genomics of a Giardia intestinalis assemblage E isolate |
title | Genome analysis and comparative genomics of a Giardia intestinalis assemblage E isolate |
title_full | Genome analysis and comparative genomics of a Giardia intestinalis assemblage E isolate |
title_fullStr | Genome analysis and comparative genomics of a Giardia intestinalis assemblage E isolate |
title_full_unstemmed | Genome analysis and comparative genomics of a Giardia intestinalis assemblage E isolate |
title_short | Genome analysis and comparative genomics of a Giardia intestinalis assemblage E isolate |
title_sort | genome analysis and comparative genomics of a giardia intestinalis assemblage e isolate |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3091692/ https://www.ncbi.nlm.nih.gov/pubmed/20929575 http://dx.doi.org/10.1186/1471-2164-11-543 |
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