Development of a recombinase-aided amplification assay for detection of orf virus

被引:17
|
作者
Wang, Yong [1 ]
Cui, Yongqiu [1 ]
Yu, Zhaorong [1 ]
Li, Yeqiu [1 ]
Bai, Caixia [1 ]
Sun, Pei [1 ]
Zhu, Wen [1 ]
Li, Yongdong [2 ]
机构
[1] Anhui Agr Univ, Coll Anim Sci & Technol, Anhui Prov Key Lab Vet Pathobiol & Dis Control, Hefei 230036, Peoples R China
[2] Ningbo Municipal Ctr Dis Control & Prevent, Municipal Key Lab Virol, Ningbo 315010, Peoples R China
基金
中国国家自然科学基金;
关键词
Recombinase-aided amplification; Orf virus; Clinical diagnosis; TIME PCR ASSAY; PHYLOGENETIC ANALYSIS; IDENTIFICATION; PROVINCE; OUTBREAK;
D O I
10.1016/j.jviromet.2020.113861
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Orf, caused by orf virus (ORFV), is an important zoonotic disease that infects goat and sheep, leading to huge economic losses. ORFV can also cause cutaneous lesions in people who come in close contact with the diseased animals. Although accurate diagnostic methods for ORFV infection exist, there is a need for a rapid, specific, and sensitive method for easy clinical application. Here, we successfully established a recombinase-aided amplification (RAA) assay for rapid detection of ORFV. The analytical sensitivity of the assay for ORFV detection is 1 x 10(1) copies per reaction. Moreover, no cross-reaction was observed with other common DNA viruses. A total of 45 archived suspected ORFV infected nasal scab skin samples were examined by RAA and SYBR Green-based real-time polymerase chain reaction (PCR). Compared with the real-time PCR assay, the kappa values of the RAA assay for ORFV detection was 0.845 (p < 0.001), indicating that both assay results were fully in agreement. In conclusion, this detection assay provides a rapid, sensitive, and specific method for ORFV detection and is suitable for ORFV clinical testing.
引用
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页数:4
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