Exploiting digital droplet PCR and Next Generation Sequencing technologies to determine the relative abundance of individual Eimeria species in a DNA sample

• Published in: Veterinary parasitology 2021-08, Vol.296, p.109443-109443, Article 109443
• Main Authors: Snyder, R.P., Guerin, M.T., Hargis, B.M., Imai, R., Kruth, P.S., Page, G., Rejman, E., Barta, J.R.
• Format: Article
• Language: English
• Subjects: Droplet digital PCR; Eimeria species; Next Generation Sequencing; Quantification
• ISSN: 0304-4017; 1873-2550
• DOI: 10.1016/j.vetpar.2021.109443

DNA-based diagnostic assays for detecting infections with Eimeria species have been limited to providing identification and presence/absence data for samples containing oocysts. Modern technologies that generate quantitative data, such as droplet digital PCR (ddPCR) and Next Generation Sequencing (NGS), utilize a relatively short amplicon size containing sufficient species-specific variation for reliable species level identification. Targeting the cytochrome c oxidase subunit III gene in the mitochondrial genome, we established protocols using these technologies to determine the relative abundance of the number of copies/μL of Eimeria species in a sample. Samples from chickens of known and unknown Eimeria species composition were analyzed to determine the suitability of these technologies as diagnostic assays. All technologies demonstrated robust capability of identifying and quantifying the Eimeria species in samples. The new quantitative assays described herein will produce invaluable detail of Eimeria species infections for an array of situations in commercial chicken production systems, enabling further characterization of the disease profile and allowing for the development or enhancement of new intervention strategies.