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Evaluation of Next-Generation Sequencing Applied to Cryptosporidium parvum and Cryptosporidium hominis Epidemiological Study

Background. Nowadays, most of the C. parvum and C. hominis epidemiological studies are based on gp60 gene subtyping using the Sanger sequencing (SgS) method. Unfortunately, SgS presents the limitation of being unable to detect mixed infections. Next-Generation Sequencing (NGS) seems to be an interes...

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Autores principales: Bailly, Eloïse, Valot, Stéphane, Vincent, Anne, Duffourd, Yannis, Grangier, Nadège, Chevarin, Martin, Costa, Damien, Razakandrainibe, Romy, Favennec, Loïc, Basmaciyan, Louise, Dalle, Frédéric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9414878/
https://www.ncbi.nlm.nih.gov/pubmed/36015058
http://dx.doi.org/10.3390/pathogens11080938
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author Bailly, Eloïse
Valot, Stéphane
Vincent, Anne
Duffourd, Yannis
Grangier, Nadège
Chevarin, Martin
Costa, Damien
Razakandrainibe, Romy
Favennec, Loïc
Basmaciyan, Louise
Dalle, Frédéric
author_facet Bailly, Eloïse
Valot, Stéphane
Vincent, Anne
Duffourd, Yannis
Grangier, Nadège
Chevarin, Martin
Costa, Damien
Razakandrainibe, Romy
Favennec, Loïc
Basmaciyan, Louise
Dalle, Frédéric
author_sort Bailly, Eloïse
collection PubMed
description Background. Nowadays, most of the C. parvum and C. hominis epidemiological studies are based on gp60 gene subtyping using the Sanger sequencing (SgS) method. Unfortunately, SgS presents the limitation of being unable to detect mixed infections. Next-Generation Sequencing (NGS) seems to be an interesting solution to overcome SgS limits. Thus, the aim of our study was to (i) evaluate the reliability of NGS as a molecular typing tool for cryptosporidiosis, (ii) investigate the genetic diversity of the parasite and the frequency of mixed infections, (iii) assess NGS usefulness in Cryptosporidium sp. outbreak investigations, and (iv) assess an interpretation threshold of sequencing data. Methods. 108 DNA extracts from positive samples were sequenced by NGS. Among them, two samples were used to validate the reliability of the subtyping obtained by NGS and its capacity to detect DNA mixtures. In parallel, 106 samples from French outbreaks were used to expose NGS to epidemic samples. Results. NGS proved suitable for Cryptosporidium sp. subtyping at the gp60 gene locus, bringing more genetic information compared to SgS, especially by working on many samples simultaneously and detecting more diversity. Conclusions. This study confirms the usefulness of NGS applied to C. hominis and C. parvum epidemiological studies, especially aimed at detecting minority variants.
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spelling pubmed-94148782022-08-27 Evaluation of Next-Generation Sequencing Applied to Cryptosporidium parvum and Cryptosporidium hominis Epidemiological Study Bailly, Eloïse Valot, Stéphane Vincent, Anne Duffourd, Yannis Grangier, Nadège Chevarin, Martin Costa, Damien Razakandrainibe, Romy Favennec, Loïc Basmaciyan, Louise Dalle, Frédéric Pathogens Article Background. Nowadays, most of the C. parvum and C. hominis epidemiological studies are based on gp60 gene subtyping using the Sanger sequencing (SgS) method. Unfortunately, SgS presents the limitation of being unable to detect mixed infections. Next-Generation Sequencing (NGS) seems to be an interesting solution to overcome SgS limits. Thus, the aim of our study was to (i) evaluate the reliability of NGS as a molecular typing tool for cryptosporidiosis, (ii) investigate the genetic diversity of the parasite and the frequency of mixed infections, (iii) assess NGS usefulness in Cryptosporidium sp. outbreak investigations, and (iv) assess an interpretation threshold of sequencing data. Methods. 108 DNA extracts from positive samples were sequenced by NGS. Among them, two samples were used to validate the reliability of the subtyping obtained by NGS and its capacity to detect DNA mixtures. In parallel, 106 samples from French outbreaks were used to expose NGS to epidemic samples. Results. NGS proved suitable for Cryptosporidium sp. subtyping at the gp60 gene locus, bringing more genetic information compared to SgS, especially by working on many samples simultaneously and detecting more diversity. Conclusions. This study confirms the usefulness of NGS applied to C. hominis and C. parvum epidemiological studies, especially aimed at detecting minority variants. MDPI 2022-08-18 /pmc/articles/PMC9414878/ /pubmed/36015058 http://dx.doi.org/10.3390/pathogens11080938 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Bailly, Eloïse
Valot, Stéphane
Vincent, Anne
Duffourd, Yannis
Grangier, Nadège
Chevarin, Martin
Costa, Damien
Razakandrainibe, Romy
Favennec, Loïc
Basmaciyan, Louise
Dalle, Frédéric
Evaluation of Next-Generation Sequencing Applied to Cryptosporidium parvum and Cryptosporidium hominis Epidemiological Study
title Evaluation of Next-Generation Sequencing Applied to Cryptosporidium parvum and Cryptosporidium hominis Epidemiological Study
title_full Evaluation of Next-Generation Sequencing Applied to Cryptosporidium parvum and Cryptosporidium hominis Epidemiological Study
title_fullStr Evaluation of Next-Generation Sequencing Applied to Cryptosporidium parvum and Cryptosporidium hominis Epidemiological Study
title_full_unstemmed Evaluation of Next-Generation Sequencing Applied to Cryptosporidium parvum and Cryptosporidium hominis Epidemiological Study
title_short Evaluation of Next-Generation Sequencing Applied to Cryptosporidium parvum and Cryptosporidium hominis Epidemiological Study
title_sort evaluation of next-generation sequencing applied to cryptosporidium parvum and cryptosporidium hominis epidemiological study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9414878/
https://www.ncbi.nlm.nih.gov/pubmed/36015058
http://dx.doi.org/10.3390/pathogens11080938
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