A novel recombinase polymerase amplification (RPA) assay for the rapid isothermal detection of Neospora caninum in aborted bovine fetuses

Tian, A.L. and Elsheikha, Hany M. and Zhou, Dong-Hui and Wu, Yao-Dong and Chen, Mu-Xin and Wang, Meng and Chen, Dan and Zhang, Xi-Chen and Zhu, Xing-Quan (2018) A novel recombinase polymerase amplification (RPA) assay for the rapid isothermal detection of Neospora caninum in aborted bovine fetuses. Veterinary Parasitology, 258 . pp. 24-29. ISSN 0304-4017

Full text not available from this repository.

Abstract

The development of a method to rapidly diagnose Neospora caninum infection is highly desirable. Recombinase polymerase amplification (RPA), combined with lateral flow (LF) strips, is a novel approach to rapidly amplify and visualize DNA. We have developed a prototype LF-RPA assay, using primers and a probe that targeted a specific sequence in the N. caninum NC-5 gene. The N. caninum-specific LF-RPA assay was first tested on purified DNA from oocysts and amplified N. caninum DNA to detectable levels in 10 min, at a constant temperature and without the need for an expensive thermocycler. The designed RPA primers and probe displayed 100% specificity for detecting N. caninum without any cross-reaction with DNA from nine related protozoan spp. (eg Toxoplasma gondii, Sarcocystis gigantean, Sarcocystis zuoi, Hammondia hammondi, Hammondia heydorni, Eimeria cylindrica, Plasmodium falciparum, Theileria annulata and Babesia bigemina). Although, LF-RPA assay detected amounts as low as 50 fg of N. caninum DNA, it was nearly 5-fold less sensitive than previously published qPCR and nested PCR assays. We tested the diagnostic performance of the LF-RPA assay for the detection of N. caninum DNA in aborted bovine fetal tissue samples, and compared the results with those obtained from nested PCR. Out of the 75 samples examined, 18 (24%) and 17 (22.6%) tested positive using LF-RPA and nested PCR, respectively. Our results indicate that LF-RPA is a suitable assay for the rapid and reliable detection of N. caninum.

Item Type: Article
RIS ID: https://nottingham-repository.worktribe.com/output/946704
Keywords: Neospora caninum; Molecular diagnostics; Isothermal amplification; Recombinase polymerase amplification(RPA); Lateral flow(LF)strips
Schools/Departments: University of Nottingham, UK > Faculty of Medicine and Health Sciences > School of Veterinary Medicine and Science
Identification Number: https://doi.org/10.1016/j.vetpar.2018.06.004
Depositing User: Eprints, Support
Date Deposited: 13 Jun 2018 12:01
Last Modified: 04 May 2020 19:46
URI: http://eprints.nottingham.ac.uk/id/eprint/52373

Actions (Archive Staff Only)

Edit View Edit View