A rapid RT-LAMP assay for the detection of all four lineages of Peste des Petits Ruminants Virus

被引:15
作者
Rajko-Nenow, Paulina [1 ]
Flannery, John [1 ]
Arnold, Hannah [1 ]
Howson, Emma L. A. [1 ]
Darpel, Karin [1 ]
Stedman, Anna [1 ]
Corla, Amanda [1 ]
Batten, Carrie [1 ]
机构
[1] Pirbright Inst, Ash Rd, Surrey GU24 ONF, England
基金
英国生物技术与生命科学研究理事会;
关键词
PPRV; RT-LAMP; Diagnostics; Outbreak; Surveillance; ISOTHERMAL AMPLIFICATION ASSAY; SENSITIVE DETECTION; PCR ASSAY; EPIDEMIOLOGY;
D O I
10.1016/j.jviromet.2019.113730
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Peste des petits ruminants (PPR) is a viral disease of small ruminants that is caused by the PPR virus (PPRV) and is a significant burden on subsistence farmers across the developing world. Loop-mediated isothermal amplification (LAMP) provides cost-effective, rapid, specific and sensitive detection of nucleic acid and has been demonstrated to have field application for a range of viruses. We describe the development of a novel PPRV RT-LAMP assay utilising carefully-selected primers (targeting the N-gene) allowing for the detection of all known PPRV lineages in < 20 min. The assay was evaluated in comparison with a "gold standard" real-time RT-PCR assay using more than 200 samples, comprising samples from recent PPRV outbreaks, experimentally-infected goats, well-characterised cell culture isolates and samples collected from uninfected animals. The RT-LAMP assay demonstrated 100% diagnostic specificity and greater than 97% diagnostic sensitivity in comparison with the real-time RT-PCR assay. The limit of detection was between 0.3 and 0.8 log(10) TCID50 ml(-1) equating to a Cr value of 31.52 to 33.48. In experimentally-infected animals, the RT-LAMP could detect PPRV as early as 4 days post infection (dpi) - before clinical signs were observed at 7 dpi. The RT-LAMP assay can support the global PPR eradication campaign.
引用
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页数:9
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