Detection of gastrointestinal nematodes (GIN) as both a qualitative and quantitative test is highly desirable. Methods such as multiplex and qPCR are capable of providing such results, but can be laborious and expensive. This paper presents a rapid, low-cost method of preparing GIN egg from faecal samples that produces DNA suitable for PCR analysis. We also describe a set of primers that are suitable for single-tube multiplex PCR.
Keywords: Gastrointestinal nematodes; Multiplex; Polymerase Chain Reaction; Primers.
Copyright © 2021 Elsevier B.V. All rights reserved.