Cargando…

Highly contiguous genomes of human clinical isolates of Giardia duodenalis reveal assemblage- and sub-assemblage-specific presence–absence variation in protein-coding genes

Giardia duodenalis (syn. G. intestinalis, G. lamblia) is a widespread gastrointestinal protozoan parasite with debated taxonomic status. Currently, eight distinct genetic sub-groups, termed assemblages A–H, are defined based on a few genetic markers. Assemblages A and B may represent distinct specie...

Descripción completa

Detalles Bibliográficos
Autores principales: Klotz, Christian, Schmid, Marc William, Winter, Katja, Ignatius, Ralf, Weisz, Filip, Saghaug, Christina Skar, Langeland, Nina, Dawson, Scott, Lalle, Marco, Hanevik, Kurt, Cacciò, Simone M., Aebischer, Toni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Microbiology Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10132058/
https://www.ncbi.nlm.nih.gov/pubmed/36976254
http://dx.doi.org/10.1099/mgen.0.000963
_version_ 1785031317788819456
author Klotz, Christian
Schmid, Marc William
Winter, Katja
Ignatius, Ralf
Weisz, Filip
Saghaug, Christina Skar
Langeland, Nina
Dawson, Scott
Lalle, Marco
Hanevik, Kurt
Cacciò, Simone M.
Aebischer, Toni
author_facet Klotz, Christian
Schmid, Marc William
Winter, Katja
Ignatius, Ralf
Weisz, Filip
Saghaug, Christina Skar
Langeland, Nina
Dawson, Scott
Lalle, Marco
Hanevik, Kurt
Cacciò, Simone M.
Aebischer, Toni
author_sort Klotz, Christian
collection PubMed
description Giardia duodenalis (syn. G. intestinalis, G. lamblia) is a widespread gastrointestinal protozoan parasite with debated taxonomic status. Currently, eight distinct genetic sub-groups, termed assemblages A–H, are defined based on a few genetic markers. Assemblages A and B may represent distinct species and are both of human public health relevance. Genomic studies are scarce and the few reference genomes available, in particular for assemblage B, are insufficient for adequate comparative genomics. Here, by combining long- and short-read sequences generated by PacBio and Illumina sequencing technologies, we provide nine annotated genome sequences for reference from new clinical isolates (four assemblage A and five assemblage B parasite isolates). Isolates chosen represent the currently accepted classification of sub-assemblages AI, AII, BIII and BIV. Synteny over the whole genome was generally high, but we report chromosome-level translocations as a feature that distinguishes assemblage A from B parasites. Orthologue gene group analysis was used to define gene content differences between assemblage A and B and to contribute a gene-set-based operational definition of respective taxonomic units. Giardia is tetraploid, and high allelic sequence heterogeneity (ASH) for assemblage B vs. assemblage A has been observed so far. Noteworthy, here we report an extremely low ASH (0.002%) for one of the assemblage B isolates (a value even lower than the reference assemblage A isolate WB-C6). This challenges the view of low ASH being a notable feature that distinguishes assemblage A from B parasites, and low ASH allowed assembly of the most contiguous assemblage B genome currently available for reference. In conclusion, the description of nine highly contiguous genome assemblies of new isolates of G. duodenalis assemblage A and B adds to our understanding of the genomics and species population structure of this widespread zoonotic parasite.
format Online
Article
Text
id pubmed-10132058
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Microbiology Society
record_format MEDLINE/PubMed
spelling pubmed-101320582023-04-27 Highly contiguous genomes of human clinical isolates of Giardia duodenalis reveal assemblage- and sub-assemblage-specific presence–absence variation in protein-coding genes Klotz, Christian Schmid, Marc William Winter, Katja Ignatius, Ralf Weisz, Filip Saghaug, Christina Skar Langeland, Nina Dawson, Scott Lalle, Marco Hanevik, Kurt Cacciò, Simone M. Aebischer, Toni Microb Genom Research Articles Giardia duodenalis (syn. G. intestinalis, G. lamblia) is a widespread gastrointestinal protozoan parasite with debated taxonomic status. Currently, eight distinct genetic sub-groups, termed assemblages A–H, are defined based on a few genetic markers. Assemblages A and B may represent distinct species and are both of human public health relevance. Genomic studies are scarce and the few reference genomes available, in particular for assemblage B, are insufficient for adequate comparative genomics. Here, by combining long- and short-read sequences generated by PacBio and Illumina sequencing technologies, we provide nine annotated genome sequences for reference from new clinical isolates (four assemblage A and five assemblage B parasite isolates). Isolates chosen represent the currently accepted classification of sub-assemblages AI, AII, BIII and BIV. Synteny over the whole genome was generally high, but we report chromosome-level translocations as a feature that distinguishes assemblage A from B parasites. Orthologue gene group analysis was used to define gene content differences between assemblage A and B and to contribute a gene-set-based operational definition of respective taxonomic units. Giardia is tetraploid, and high allelic sequence heterogeneity (ASH) for assemblage B vs. assemblage A has been observed so far. Noteworthy, here we report an extremely low ASH (0.002%) for one of the assemblage B isolates (a value even lower than the reference assemblage A isolate WB-C6). This challenges the view of low ASH being a notable feature that distinguishes assemblage A from B parasites, and low ASH allowed assembly of the most contiguous assemblage B genome currently available for reference. In conclusion, the description of nine highly contiguous genome assemblies of new isolates of G. duodenalis assemblage A and B adds to our understanding of the genomics and species population structure of this widespread zoonotic parasite. Microbiology Society 2023-03-28 /pmc/articles/PMC10132058/ /pubmed/36976254 http://dx.doi.org/10.1099/mgen.0.000963 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License.
spellingShingle Research Articles
Klotz, Christian
Schmid, Marc William
Winter, Katja
Ignatius, Ralf
Weisz, Filip
Saghaug, Christina Skar
Langeland, Nina
Dawson, Scott
Lalle, Marco
Hanevik, Kurt
Cacciò, Simone M.
Aebischer, Toni
Highly contiguous genomes of human clinical isolates of Giardia duodenalis reveal assemblage- and sub-assemblage-specific presence–absence variation in protein-coding genes
title Highly contiguous genomes of human clinical isolates of Giardia duodenalis reveal assemblage- and sub-assemblage-specific presence–absence variation in protein-coding genes
title_full Highly contiguous genomes of human clinical isolates of Giardia duodenalis reveal assemblage- and sub-assemblage-specific presence–absence variation in protein-coding genes
title_fullStr Highly contiguous genomes of human clinical isolates of Giardia duodenalis reveal assemblage- and sub-assemblage-specific presence–absence variation in protein-coding genes
title_full_unstemmed Highly contiguous genomes of human clinical isolates of Giardia duodenalis reveal assemblage- and sub-assemblage-specific presence–absence variation in protein-coding genes
title_short Highly contiguous genomes of human clinical isolates of Giardia duodenalis reveal assemblage- and sub-assemblage-specific presence–absence variation in protein-coding genes
title_sort highly contiguous genomes of human clinical isolates of giardia duodenalis reveal assemblage- and sub-assemblage-specific presence–absence variation in protein-coding genes
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10132058/
https://www.ncbi.nlm.nih.gov/pubmed/36976254
http://dx.doi.org/10.1099/mgen.0.000963
work_keys_str_mv AT klotzchristian highlycontiguousgenomesofhumanclinicalisolatesofgiardiaduodenalisrevealassemblageandsubassemblagespecificpresenceabsencevariationinproteincodinggenes
AT schmidmarcwilliam highlycontiguousgenomesofhumanclinicalisolatesofgiardiaduodenalisrevealassemblageandsubassemblagespecificpresenceabsencevariationinproteincodinggenes
AT winterkatja highlycontiguousgenomesofhumanclinicalisolatesofgiardiaduodenalisrevealassemblageandsubassemblagespecificpresenceabsencevariationinproteincodinggenes
AT ignatiusralf highlycontiguousgenomesofhumanclinicalisolatesofgiardiaduodenalisrevealassemblageandsubassemblagespecificpresenceabsencevariationinproteincodinggenes
AT weiszfilip highlycontiguousgenomesofhumanclinicalisolatesofgiardiaduodenalisrevealassemblageandsubassemblagespecificpresenceabsencevariationinproteincodinggenes
AT saghaugchristinaskar highlycontiguousgenomesofhumanclinicalisolatesofgiardiaduodenalisrevealassemblageandsubassemblagespecificpresenceabsencevariationinproteincodinggenes
AT langelandnina highlycontiguousgenomesofhumanclinicalisolatesofgiardiaduodenalisrevealassemblageandsubassemblagespecificpresenceabsencevariationinproteincodinggenes
AT dawsonscott highlycontiguousgenomesofhumanclinicalisolatesofgiardiaduodenalisrevealassemblageandsubassemblagespecificpresenceabsencevariationinproteincodinggenes
AT lallemarco highlycontiguousgenomesofhumanclinicalisolatesofgiardiaduodenalisrevealassemblageandsubassemblagespecificpresenceabsencevariationinproteincodinggenes
AT hanevikkurt highlycontiguousgenomesofhumanclinicalisolatesofgiardiaduodenalisrevealassemblageandsubassemblagespecificpresenceabsencevariationinproteincodinggenes
AT cacciosimonem highlycontiguousgenomesofhumanclinicalisolatesofgiardiaduodenalisrevealassemblageandsubassemblagespecificpresenceabsencevariationinproteincodinggenes
AT aebischertoni highlycontiguousgenomesofhumanclinicalisolatesofgiardiaduodenalisrevealassemblageandsubassemblagespecificpresenceabsencevariationinproteincodinggenes