Abstract

Cooperia sp. and Ostertagia sp. are two cosmopolitan parasitic nematodes often found in mixed gastrointestinal infections in cattle across temperate regions. In light of the recent increase in the emergence of anthelmintic resistance in these and other nematodes derived from cattle around the globe, and their negative impact on animal health and productivity, novel molecular assays need to be put forth in order to facilitate the monitoring of parasite burden in infected herds, using pasture and/or fecal samples. Here, we describe a novel droplet digital PCR platform–based concept for precise identification and quantification of the two most abundant and important parasite genera in grazing western European cattle. By exploiting a single nucleotide difference in the two parasites’ ITS2 sequence regions, we have developed two specific hydrolysis probes labeled with FAM™ or HEX™ fluorophores, which can not only distinguish between the DNA sequences of the two, but also quantify them in mixed DNA samples. A third, newly developed universal probe was also tested along the genus-specific probes to provide a robust and accurate reference. It was evident that the universal probe displayed congruent results to those obtained by the genus-specific probes when used with DNA from both parasites in a single sample. All in all, the results of our assay suggest that this novel protocol could be used to distinguish and quantify cattle parasites belonging to the two most important genera (i.e., Cooperia and Ostertagia) in a single mixed DNA sample.

Highlights

  • Infections with parasitic nematodes in cattle yield poor outcomes for both the animal(s) and the industry

  • Whereas Cooperia is mostly abundant in younger cattle and does not constitute a grave threat, worms belonging to the genus Ostertagia are known to induce severe pathological

  • The majority of work and effort into improving the detection of nematode parasites in livestock go into the small ruminant sector, where the problem of drugresistant worms is the most severe (Wolstenholme et al 2004). We address this knowledge gap between cattle and small ruminants by describing a novel assay concept that relies on the ddPCR platform for the detection and quantification of Cooperia and Ostertagia genus-specific DNA

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Summary

Introduction

Infections with parasitic nematodes in cattle yield poor outcomes for both the animal(s) and the industry. Gastrointestinal nematode (GIN) infections in ruminants often tend to be mixed, the most commonly encountered genera in European cattle are Cooperia and Ostertagia (Craig 2018). We address this knowledge gap between cattle and small ruminants by describing a novel assay concept that relies on the ddPCR platform for the detection and quantification of Cooperia and Ostertagia genus-specific DNA. The presented ddPCR assay results constitute an important stepping stone towards the development of an improved diagnostic tool, used in the monitoring of relative influence of both of these omnipresent parasite genera in grazing cattle herds. It was decided to only keep the sequences belonging to the two most well-known and studied species in European cattle—Cooperia oncophora and Ostertagia ostertagi. All downloaded sequences for each parasite species were aligned using CodonCode Aligner (v. 8.0.1), and the subsequent consensus sequences for both parasite species were inspected and compared

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