Polymerase chain reaction combined with fluorescent lateral flow immunoassay based on magnetic purification for rapid detection of canine parvovirus 2

被引:26
|
作者
Zhuang, Linlin [1 ,2 ]
Ji, Yongxin [3 ]
Tian, Peilong [1 ,2 ]
Wang, Kaixuan [1 ,2 ]
Kou, Chengkun [3 ]
Gu, Ning [1 ,2 ]
Zhang, Yu [1 ,2 ]
机构
[1] Southeast Univ, Sch Biol Sci & Med Engn, Jiangsu Key Lab Biomat & Devices, State Key Lab Bioelect, 2 Sipailou, Nanjing 210096, Jiangsu, Peoples R China
[2] Southeast Univ, Collaborat Innovat Ctr Suzhou Nano Sci & Technol, 2 Sipailou, Nanjing 210096, Jiangsu, Peoples R China
[3] Nanjing Nanoeast Biotech Co Ltd, Nanjing 210009, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Canine parvovirus; Polymerase chain reaction; Fluorescent lateral flow immunoassay; Magnetic purification; SENSITIVE DETECTION; PCR; TYPE-2; BEADS; DOGS; SEPARATION; INFECTION; FECES; ASSAY;
D O I
10.1186/s12917-019-1774-3
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
BackgroundCanine parvovirus 2 (CPV-2) is one of the most common etiological agents that cause severe gastroenteritis in puppies. Early accurate diagnosis is important for infected dogs. In recent years, magnetic separation has become an efficient and useful tool for bioassays. In this study, polymerase chain reaction (PCR) combined with fluorescent lateral flow immunoassay (LFIA) based on magnetic purification assay was developed for the quantitative detection of CPV-2.ResultsThe optimum working reaction volume and reaction time for LFIA was 100L and 2min, respectively. The PCR-LFIA assay only detected CPV-2, and did not show cross-detection of non-CPV strains. Experiments showed analytical sensitivity of 3x10(1) copies/L and demonstrated the PCR-LFIA has a diagnostic agreement of 100% with conventional PCR on detection of clinical samples (22.6% positive, 14/62). Cutoff value is 146. The results were further verified by sequencing and BLAST software. The entire process from PCR step only takes 80min.ConclusionsThis approach provides an attractive platform for rapid and quantitative detection of CPV-2, indicating great promise as a convenient molecular detection tool to facilitate disease outbreak investigations and response timely.
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页数:13
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