Development of a targeted amplicon sequencing method for genotyping Cyclospora cayetanensis from fresh produce and clinical samples with enhanced genomic resolution and sensitivity

Susan R Leonard; Mark K Mammel; Baback Gharizadeh; Sonia Almeria; Zhihai Ma; David J Lipman; Mary E Torrence; Chunlin Wang; Steven M Musser

doi:10.3389/fmicb.2023.1212863

Development of a targeted amplicon sequencing method for genotyping Cyclospora cayetanensis from fresh produce and clinical samples with enhanced genomic resolution and sensitivity

Front Microbiol. 2023 Jun 16:14:1212863. doi: 10.3389/fmicb.2023.1212863. eCollection 2023.

Authors

Susan R Leonard¹, Mark K Mammel¹, Baback Gharizadeh², Sonia Almeria¹, Zhihai Ma², David J Lipman³, Mary E Torrence¹, Chunlin Wang², Steven M Musser³

Affiliations

¹ Office of Applied Research and Safety Assessment, Center for Food Safety and Applied Nutrition, U.S. Food and Drug Administration, Laurel, MD, United States.
² Chapter Diagnostics, Menlo Park, CA, United States.
³ Center for Food Safety and Applied Nutrition, U.S. Food and Drug Administration, College Park, MD, United States.

Abstract

Outbreaks of cyclosporiasis, an enteric illness caused by the parasite Cyclospora cayetanensis, have been associated with consumption of various types of fresh produce. Although a method is in use for genotyping C. cayetanensis from clinical specimens, the very low abundance of C. cayetanensis in food and environmental samples presents a greater challenge. To complement epidemiological investigations, a molecular surveillance tool is needed for use in genetic linkage of food vehicles to cyclosporiasis illnesses, estimation of the scope of outbreaks or clusters of illness, and determination of geographical areas involved. We developed a targeted amplicon sequencing (TAS) assay that incorporates a further enrichment step to gain the requisite sensitivity for genotyping C. cayetanensis contaminating fresh produce samples. The TAS assay targets 52 loci, 49 of which are located in the nuclear genome, and encompasses 396 currently known SNP sites. The performance of the TAS assay was evaluated using lettuce, basil, cilantro, salad mix, and blackberries inoculated with C. cayetanensis oocysts. A minimum of 24 markers were haplotyped even at low contamination levels of 10 oocysts in 25 g leafy greens. The artificially contaminated fresh produce samples were included in a genetic distance analysis based on haplotype presence/absence with publicly available C. cayetanensis whole genome sequence assemblies. Oocysts from two different sources were used for inoculation, and samples receiving the same oocyst preparation clustered together, but separately from the other group, demonstrating the utility of the assay for genetically linking samples. Clinical fecal samples with low parasite loads were also successfully genotyped. This work represents a significant advance in the ability to genotype C. cayetanensis contaminating fresh produce along with greatly expanding the genomic diversity included for genetic clustering of clinical specimens.

Keywords: bait-capture; cyclosporiasis; epidemiology; foodborne parasite; genetic clustering; targeted amplicon sequencing.