Evaluation of Next-Generation Sequencing Applied to <em>Cryptosporidium parvum</em> and <em>Cryptosporidium hominis</em> Epidemiological Study
Eloïse Bailly,
Stéphane Valot,
Anne Vincent,
Yannis Duffourd,
Nadège Grangier,
Martin Chevarin,
Damien Costa,
Romy Razakandrainibe,
Loïc Favennec,
Louise Basmaciyan,
Frédéric Dalle
Affiliations
Eloïse Bailly
Parasitology-Mycology Laboratory, University Hospital Biology Platform, Dijon University Hospital Center, 21000 Dijon, France
Stéphane Valot
Parasitology-Mycology Laboratory, University Hospital Biology Platform, Dijon University Hospital Center, 21000 Dijon, France
Anne Vincent
Parasitology-Mycology Laboratory, University Hospital Biology Platform, Dijon University Hospital Center, 21000 Dijon, France
Yannis Duffourd
Inserm UMR 1231 GAD, Genetics of Developmental Disorders, Bourgogne-Franche Comté University, FHU TRANSLAD, 21000 Dijon, France
Nadège Grangier
Associated Laboratory CNR-LE for Cryptosporidiosis, University Hospital Biology Platform, Dijon University Hospital Center, 21000 Dijon, France
Martin Chevarin
Inserm UMR 1231 GAD, Genetics of Developmental Disorders, Bourgogne-Franche Comté University, FHU TRANSLAD, 21000 Dijon, France
Damien Costa
CNR LE for Cryptosporidiosis (National Center of Reference for Cryptosporidiosis, Expert Laboratory), Santé Publique France, Rouen University Hospital Center, 76031 Rouen, France
Romy Razakandrainibe
CNR LE for Cryptosporidiosis (National Center of Reference for Cryptosporidiosis, Expert Laboratory), Santé Publique France, Rouen University Hospital Center, 76031 Rouen, France
Loïc Favennec
CNR LE for Cryptosporidiosis (National Center of Reference for Cryptosporidiosis, Expert Laboratory), Santé Publique France, Rouen University Hospital Center, 76031 Rouen, France
Louise Basmaciyan
Parasitology-Mycology Laboratory, University Hospital Biology Platform, Dijon University Hospital Center, 21000 Dijon, France
Frédéric Dalle
Parasitology-Mycology Laboratory, University Hospital Biology Platform, Dijon University Hospital Center, 21000 Dijon, France
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.