Journal Article

Generation of whole genome sequences of new Cryptosporidium hominis and Cryptosporidium parvum isolates directly from stool samples

Robinson, Guy, Alexander, Jenna, Hegarty, Matthew J., Swain, Martin T., Cameron, Simon JS, Chalmers, Rachel M., Pachebat, Justin A., Hadfield, Stephen J., Elwin, Kristin

2015

Overview

Background Whole genome sequencing (WGS) of Cryptosporidium spp. has previously relied on propagation of the parasite in animals to generate enough oocysts from which to extract DNA of sufficient quantity and purity for analysis. We have developed and validated a method for preparation of genomic Cryptosporidium DNA suitable for WGS directly from human stool samples and used it to generate 10 high-quality whole Cryptosporidium genome assemblies. Our method uses a combination of salt flotation, immunomagnetic separation (IMS), and surface sterilisation of oocysts prior to DNA extraction, with subsequent use of the transposome-based Nextera XT kit to generate libraries for sequencing on Illumina platforms. IMS was found to be superior to caesium chloride density centrifugation for purification of oocysts from small volume stool samples and for reducing levels of contaminant DNA. Results The IMS-based method was used initially to sequence whole genomes of Cryptosporidium hominis gp60 subtype IbA10G2 and Cryptosporidium parvum gp60 subtype IIaA19G1R2 from small amounts of stool left over from diagnostic testing of clinical cases of cryptosporidiosis. The C. parvum isolate was sequenced to a mean depth of 51.8X with reads covering 100 % of the bases of the C. parvum Iowa II reference genome (Bioproject PRJNA 15586), while the C. hominis isolate was sequenced to a mean depth of 34.7X with reads covering 98 % of the bases of the C. hominis TU502 v1 reference genome (Bioproject PRJNA 15585). The method was then applied to a further 17 stools, successfully generating another eight new whole genome sequences, of which two were C. hominis ( gp60 subtypes IbA10G2 and IaA14R3) and six C. parvum ( gp60 subtypes IIaA15G2R1 from three samples, and one each of IIaA17G1R1, IIaA18G2R1, and IIdA22G1), demonstrating the utility of this method to sequence Cryptosporidium genomes directly from clinical samples. This development is especially important as it reduces the requirement to propagate Cryptosporidium oocysts in animal models prior to genome sequencing. Conclusion This represents the first report of high-quality whole genome sequencing of Cryptosporidium isolates prepared directly from human stool samples.

• Publisher: BioMed Central,BioMed Central Ltd,Springer Nature B.V
• Subject: Analysis / Animal Genetics and Genomics / Animal models / Base Sequence / Biomedical and Life Sciences / Centrifugation / Contaminants / Cryptosporidiosis / Cryptosporidium / Cryptosporidium - genetics / Cryptosporidium - isolation & purification / Cryptosporidium parvum - genetics / Cryptosporidium parvum - isolation & purification / Deoxyribonucleic acid / DNA / DNA, Protozoan - genetics / Eukaryote microbial genomics / Feces - parasitology / Flotation / Genetic aspects / Genome / Genomics / High-Throughput Nucleotide Sequencing / Humans / Life Sciences / Microarrays / Microbial Genetics and Genomics / Oocysts / Oocysts - metabolism / Parasites / Pilot Projects / Plant Genetics and Genomics / Proteomics / Research Article