Comparative genomics of Giardia duodenalis sub-assemblage AI beaver (Be-2) and human (WB-C6) strains show remarkable homozygosity, sequence similarity, and conservation of VSP genes
Giardia duodenalis, a major cause of waterborne infection, infects a wide range of mammalian hosts and is subdivided into eight genetically well-defined assemblages named A through H. However, fragmented genomes and a lack of comparative analysis within and between the assemblages render unclear the...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2024
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- eng
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/44791
- Acceso en línea:
- https://doi.org/10.1038/s41598-024-63783-5
https://repository.urosario.edu.co/handle/10336/44791
- Palabra clave:
- Long-read sequencing
Genome assembly
Giardia
Annotation
Ploidy
Synteny
- Rights
- License
- Attribution-NonCommercial-NoDerivatives 4.0 International
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ecfb9890-5303-4a45-bf32-71f989e55cedabcf58ba-2453-42c5-a1bd-922d7ca80a4106d7faaf-6fed-4d42-8134-2a7226f02b15bcf8bbb6-b0e6-4d01-a38f-9a30ce35ca1ed04b7d2f-97c6-45ac-933b-bbc9f523bd8d6eb99bb8-3814-439a-a605-2fa35ef94e2904ac44f5-b177-4663-825a-0f2ef51fc69194e76a16-100b-44f1-bc70-bfbb1589a25b2025-01-26T18:27:45Z2025-01-26T18:27:45Z2024-12-012024-12-01Giardia duodenalis, a major cause of waterborne infection, infects a wide range of mammalian hosts and is subdivided into eight genetically well-defined assemblages named A through H. However, fragmented genomes and a lack of comparative analysis within and between the assemblages render unclear the molecular mechanisms controlling host specificity and differential disease outcomes. To address this, we generated a near-complete de novo genome of AI assemblage using the Oxford Nanopore platform by sequencing the Be-2 genome. We generated 148,144 long-reads with quality scores of > 7. The final genome assembly consists of only nine contigs with an N50 of 3,045,186 bp. This assembly agrees closely with the assembly of another strain in the AI assemblage (WB-C6). However, a critical difference is that a region previously placed in the five-prime region of Chr5 belongs to Chr4 of Be-2. We find a high degree of conservation in the ploidy, homozygosity, and the presence of cysteine-rich variant-specific surface proteins (VSPs) within the AI assemblage. Our assembly provides a nearly complete genome of a member of the AI assemblage of G. duodenalis, aiding population genomic studies capable of elucidating Giardia transmission, host range, and pathogenicity.application/pdfhttps://doi.org/10.1038/s41598-024-63783-5https://repository.urosario.edu.co/handle/10336/44791engScientific ReportsScientific ReportsAttribution-NonCommercial-NoDerivatives 4.0 InternationalAbierto (Texto Completo)http://creativecommons.org/licenses/by-nc-sa/4.0/http://purl.org/coar/access_right/c_abf2Scientific Reportsinstname:Universidad del Rosarioreponame:Repositorio Institucional EdocURLong-read sequencingGenome assemblyGiardiaAnnotationPloidySyntenyComparative genomics of Giardia duodenalis sub-assemblage AI beaver (Be-2) and human (WB-C6) strains show remarkable homozygosity, sequence similarity, and conservation of VSP genesarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Rodrigo de Paula BaptistaMatthew S. TuckerMatthew J. ValenteSubodh K. SrivastavaNadya Chehab, Alison LiJahangheer S. ShaikJuan David RamirezBenjamin M. Rosenthal,Asis KhanORIGINALComparative_genomics_of_Giardia_duodenalis_sub-assemblage_AI_beaver.pdfapplication/pdf2400899https://repository.urosario.edu.co/bitstreams/67940d6e-932c-49cf-8fbb-b9a460250d28/download1c3c6c9dc03c735f6d5044571ec6e598MD51TEXTComparative_genomics_of_Giardia_duodenalis_sub-assemblage_AI_beaver.pdf.txtComparative_genomics_of_Giardia_duodenalis_sub-assemblage_AI_beaver.pdf.txtExtracted texttext/plain58349https://repository.urosario.edu.co/bitstreams/26f7b881-6343-4de7-9f19-001120b2c07c/download8983c3537c51a1cac3fe00458a38657cMD52THUMBNAILComparative_genomics_of_Giardia_duodenalis_sub-assemblage_AI_beaver.pdf.jpgComparative_genomics_of_Giardia_duodenalis_sub-assemblage_AI_beaver.pdf.jpgGenerated Thumbnailimage/jpeg4992https://repository.urosario.edu.co/bitstreams/3d7a24da-414c-43b7-ae23-b43247e63f90/downloadd1a6f876a6085067f0e9bebc525446e0MD5310336/44791oai:repository.urosario.edu.co:10336/447912025-01-27 03:06:26.471http://creativecommons.org/licenses/by-nc-sa/4.0/Attribution-NonCommercial-NoDerivatives 4.0 Internationalhttps://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co |
dc.title.spa.fl_str_mv |
Comparative genomics of Giardia duodenalis sub-assemblage AI beaver (Be-2) and human (WB-C6) strains show remarkable homozygosity, sequence similarity, and conservation of VSP genes |
title |
Comparative genomics of Giardia duodenalis sub-assemblage AI beaver (Be-2) and human (WB-C6) strains show remarkable homozygosity, sequence similarity, and conservation of VSP genes |
spellingShingle |
Comparative genomics of Giardia duodenalis sub-assemblage AI beaver (Be-2) and human (WB-C6) strains show remarkable homozygosity, sequence similarity, and conservation of VSP genes Long-read sequencing Genome assembly Giardia Annotation Ploidy Synteny |
title_short |
Comparative genomics of Giardia duodenalis sub-assemblage AI beaver (Be-2) and human (WB-C6) strains show remarkable homozygosity, sequence similarity, and conservation of VSP genes |
title_full |
Comparative genomics of Giardia duodenalis sub-assemblage AI beaver (Be-2) and human (WB-C6) strains show remarkable homozygosity, sequence similarity, and conservation of VSP genes |
title_fullStr |
Comparative genomics of Giardia duodenalis sub-assemblage AI beaver (Be-2) and human (WB-C6) strains show remarkable homozygosity, sequence similarity, and conservation of VSP genes |
title_full_unstemmed |
Comparative genomics of Giardia duodenalis sub-assemblage AI beaver (Be-2) and human (WB-C6) strains show remarkable homozygosity, sequence similarity, and conservation of VSP genes |
title_sort |
Comparative genomics of Giardia duodenalis sub-assemblage AI beaver (Be-2) and human (WB-C6) strains show remarkable homozygosity, sequence similarity, and conservation of VSP genes |
dc.subject.spa.fl_str_mv |
Long-read sequencing Genome assembly Giardia Annotation Ploidy Synteny |
topic |
Long-read sequencing Genome assembly Giardia Annotation Ploidy Synteny |
description |
Giardia duodenalis, a major cause of waterborne infection, infects a wide range of mammalian hosts and is subdivided into eight genetically well-defined assemblages named A through H. However, fragmented genomes and a lack of comparative analysis within and between the assemblages render unclear the molecular mechanisms controlling host specificity and differential disease outcomes. To address this, we generated a near-complete de novo genome of AI assemblage using the Oxford Nanopore platform by sequencing the Be-2 genome. We generated 148,144 long-reads with quality scores of > 7. The final genome assembly consists of only nine contigs with an N50 of 3,045,186 bp. This assembly agrees closely with the assembly of another strain in the AI assemblage (WB-C6). However, a critical difference is that a region previously placed in the five-prime region of Chr5 belongs to Chr4 of Be-2. We find a high degree of conservation in the ploidy, homozygosity, and the presence of cysteine-rich variant-specific surface proteins (VSPs) within the AI assemblage. Our assembly provides a nearly complete genome of a member of the AI assemblage of G. duodenalis, aiding population genomic studies capable of elucidating Giardia transmission, host range, and pathogenicity. |
publishDate |
2024 |
dc.date.created.spa.fl_str_mv |
2024-12-01 |
dc.date.issued.spa.fl_str_mv |
2024-12-01 |
dc.date.accessioned.none.fl_str_mv |
2025-01-26T18:27:45Z |
dc.date.available.none.fl_str_mv |
2025-01-26T18:27:45Z |
dc.type.spa.fl_str_mv |
article |
dc.type.coarversion.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
dc.type.coar.fl_str_mv |
http://purl.org/coar/resource_type/c_6501 |
dc.type.spa.spa.fl_str_mv |
Artículo |
dc.identifier.doi.spa.fl_str_mv |
https://doi.org/10.1038/s41598-024-63783-5 |
dc.identifier.uri.none.fl_str_mv |
https://repository.urosario.edu.co/handle/10336/44791 |
url |
https://doi.org/10.1038/s41598-024-63783-5 https://repository.urosario.edu.co/handle/10336/44791 |
dc.language.iso.spa.fl_str_mv |
eng |
language |
eng |
dc.relation.ispartof.spa.fl_str_mv |
Scientific Reports |
dc.rights.spa.fl_str_mv |
Attribution-NonCommercial-NoDerivatives 4.0 International |
dc.rights.coar.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 |
dc.rights.acceso.spa.fl_str_mv |
Abierto (Texto Completo) |
dc.rights.uri.spa.fl_str_mv |
http://creativecommons.org/licenses/by-nc-sa/4.0/ |
rights_invalid_str_mv |
Attribution-NonCommercial-NoDerivatives 4.0 International Abierto (Texto Completo) http://creativecommons.org/licenses/by-nc-sa/4.0/ http://purl.org/coar/access_right/c_abf2 |
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application/pdf |
dc.publisher.spa.fl_str_mv |
Scientific Reports |
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Scientific Reports |
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Universidad del Rosario |
dc.source.instname.spa.fl_str_mv |
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